Jobs at UCB Pharma

Statistical Methodologist (UK) (Slough, Berkshire, GB)

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We are looking for a Statistical Methodologist who is curious, collaborative, and impact-focused to join us in our Biometrics and Data Science team, based in any of our Brussels (Belgium), Monheim (Germany), Slough (UK) or Raleigh (US) offices.

About the role

You will help shape how evidence is generated and communicated across the drug development lifecycle—from early clinical development to regulatory approval and lifecycle work. You will provide expert statistical consultation on trial design and analysis, develop and apply advanced methods, and translate complex quantitative concepts into clear insights for cross-functional partners. You will also contribute to scientific communications and external collaboration through publications and industry initiatives.

Who you’ll work with

You will be working in a team that provides statistical consultancy across therapy areas and development stages, partnering closely with colleagues in clinical development, regulatory strategy, data science, and medical affairs. The team values practical innovation, clear communication, and collaboration—bringing novel statistical approaches into real study decisions and sharing learnings with the wider scientific community.

What you’ll do

Provide statistical consultation on clinical trial design and analysis across multiple development stages and therapy areas.
Develop and implement innovative statistical approaches, including model-based methods using frequentist and Bayesian techniques.
Run or guide advanced analyses and simulations to inform design options, sample size, and power trade-offs.
Communicate complex quantitative topics clearly using visuals, simulations, and plain language for diverse audiences.
Contribute to internal learning by delivering training on advanced statistical concepts for non-statisticians and statisticians.
Contribute to the group’s external profile through scientific publications, conference presentations, and participation in cross-industry initiatives and working groups

Interested? For this position you’ll need the following education, experience and skills:

Doctoral degree in statistics, mathematics, or a closely related scientific discipline.
Experience in statistical methodology for clinical development (early to late stage); direct entry may be considered.
Strong statistical programming skills (R preferred; equivalent tools considered).
Working knowledge of global clinical trial guidelines and major health authority expectations is an advantage.
Ability to work effectively with autonomy, manage multiple priorities, and deliver timely, high-quality outputs.
Clear written and spoken communication in English, including the ability to explain statistics to non-technical audiences.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Patient Evidence and Communities Learning Partner (Slough, Berkshire, GB)

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We are looking for a Patient Evidence Communities Learning Partner who is curious, collaborative, and impact-focused to join us in our Learning Patient Evidence & Impact team, based in our Slough office in the United Kingdom.

About the role

You will design and deliver learning solutions that strengthen capabilities across patient evidence communities, a key business division for UCB. Acting as a strategic partner, you will translate business priorities and capability gaps into structured learning journeys that drive measurable impact, adoption, and continuous improvement across teams.

Who you’ll work with

You will be working in a team that collaborates closely with patient evidence, stakeholder integration, and patient community-focused colleagues across global, regional, and local levels. You will partner with talent professionals, subject experts, and external partners to create practical, engaging learning experiences embedded in everyday work.

What you’ll do

• Partner with business and talent colleagues to align learning priorities with strategic goals and capability needs.

• Design structured, competency-based learning journeys that support knowledge, skills, and behavior development.

• Lead learning needs analysis and translate insights into clear, actionable learning plans.

• Coordinate and deliver learning programs across virtual, hybrid, and in-person formats.

• Support stakeholder engagement and change adoption through clear communication and storytelling.

• Measure learning effectiveness using qualitative and quantitative data to drive continuous improvement.

Interested?

For this role we’re looking for the following education, experience and skills:

• University degree with proven experience in health sciences, evidence generation, regulatory, medical, markets access, RWE or related fields preferably in the biopharmaceutical industry.

• Several years of experience designing and delivering impactful learning programs in complex organizations.

• Strong understanding of adult learning principles and modern learning design approaches.

• Proven ability to manage projects, work across functions, and balance multiple priorities.

• Confident communicator who builds trust and influences through collaboration.

• Comfortable working with data to identify trends, evaluate impact, and improve learning outcomes.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Market Access Learning Lead - Europe & Intercontinental (Slough, Berkshire, GB)

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We are looking for a Market Access Learning Lead – Europe & Intercontinental who is strategic, collaborative, and impact-driven to join us in our Learning Patient Evidence & Impact team, based in our Slough office in the United Kingdom.

About the role

You will shape and deliver a regional learning strategy that strengthens Market Access, Pricing, and Policy capabilities across Europe and intercontinental markets. Working closely with cross-functional partners, you will translate evolving access and reimbursement landscapes into practical, high-impact learning journeys that support decision-making, performance, and business outcomes.

Who you’ll work with

You will be working in a diverse, international team that partners closely with Market Access, Pricing, Policy, Evidence, Corporate Affairs, and Commercial teams. You will collaborate with global learning colleagues, subject-matter experts, and local teams to deliver consistent, relevant, and engaging learning experiences across markets.

What you’ll do

• Own and evolve the regional Market Access and Pricing learning strategy aligned with business priorities and policy trends.

• Translate complex access, pricing, and reimbursement changes into clear capability and learning priorities.

• Design and deliver end-to-end learning journeys, including role-based capability frameworks and launch readiness programs.

• Partner with cross-functional stakeholders and learning experts to ensure practical, scientifically sound learning solutions.

• Oversee regional rollout, localization, and adoption of learning initiatives across markets.

• Measure learning impact, track capability progress, and continuously improve solutions using data and insights.

Interested?

For this role we’re looking for the following education, experience and skills:

• Bachelor’s degree required; advanced degree in life sciences, health economics, public health, or related field preferred.

• Several years of experience in pharmaceutical Market Access, Pricing, Policy, HEOR, RWE or related roles across multiple ecosystems.

• Strong understanding of European and Intercontinental Payer landscape differences, pricing, and reimbursement environments.

• Proven experience translating complex topics into engaging, actionable learning solutions.

• Confident stakeholder partner with strong facilitation, collaboration, and influencing skills.

• Comfortable working across cultures, functions, and changing environments.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global Regulatory Affairs CMC Lead (Slough, Berkshire, GB)

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We are looking for a Global Regulatory Affairs CMC Lead who is collaborative, strategic, and delivery focused to join us in our Global Regulatory Affairs team, based in any of our Brussels (Belgium), Slough (UK) or Atlanta/Raleigh (US) offices.

About the role

You will lead regulatory strategies, planning and preparation of global or regional specific CMC submissions for assigned projects/products across the full product lifecycle, from early development to post approval. Working closely with cross functional teams, you will shape high quality regulatory documentation, engage with health authorities, and support timely approvals that meet patient and business needs. This role plays a key part in ensuring regulatory excellence and continuous improvement across global markets.

Who you’ll work with

You will be working in a team that brings together regulatory, manufacturing, quality, and supply experts from around the world. The team collaborates closely with other functions in global regulatory affairs, and development, technical and supply teams, creating strong partnerships to support innovative therapies. You will also engage with global stakeholders and external authorities, contributing your expertise across cross-functional projects.

What you’ll do

Define and deliver regulatory strategies for global or regional specific CMC submissions for assigned projects/products across development and post approval stages.
Lead complex regulatory submissions, ensuring consistency, quality, and alignment with agreed global strategies.
Author and review regulatory CMC documentation within agreed timelines.
Represent regulatory CMC expertise in cross functional project teams and authority interactions, as needed.
Anticipate risks across the product lifecycle and communicate solutions clearly to key stakeholders.
Support process improvement initiatives and mentor colleagues within the regulatory team.

Interested? For this position you’ll need the following education, experience and skills:

A degree in a scientific or technical discipline; advanced or regulatory qualifications are an advantage.
Extensive experience in pharmaceutical industry and in regulatory roles, including global submissions and working with health authorities supporting regulatory discussions
Excellence and proven track record of successful regulatory strategic authoring and contribution to delivering regulatory CMC documentation of new marketing authorisations, clinical trial applications and post-approval submissions.
Experience working with health authorities and supporting regulatory discussions and responses.
Demonstrated ability to leverage digital tools, structured data, and regulatory information systems to enhance regulatory strategy, submission quality, lifecycle management, and decision‑making across global markets.
Ability to participate or lead and embed digital and process innovation initiatives within the team, driving harmonization, efficiency, and regulatory excellence across cross‑functional and global teams.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Biological Services Unit Technician (Slough, Berkshire, GB)

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We are looking for a Technician who is agile and innovative to join our Biological Services Unit, based in Slough, UK (Windlesham 2026/2027).

About the role

We have an opportunity for an experienced licensed animal technician to join our leading research establishment.

The BSU plays a crucial role in UCB’s drug discovery platform. When it’s necessary to conduct in-vivo experiments, we are dedicated to providing the highest welfare standards and always consider ethical implications.

The staff in the unit are specialists in providing practical in-vivo support and advise for scientists, as well as providing an outstanding environment and care for the animals housed. Optimising housing conditions, reducing stress, and refining all human interactions with our animals are key to our ethics, standards and scientific models. We expect the Technicians to be proactive with these refinements and set examples for the unit.

The facilities will fully relocate to Windlesham, Surrey in early 2027; however, some travel will be required toward the end of 2026. Staff will be expected to support the preparation and transition activities, including establishing processes at the new facility to ensure regulatory compliance and to facilitate the successful introduction of animals in optimal conditions.

You will be able to work as a team, with a flexible approach. To work additional hours when required, this will include occasional weekends (1 in 4) and Bank Holidays.

Who you’ll work with

Our small team in the BSU and scientists.

What you’ll do

Responsible for keeping all animal room areas clean and tidy, in alignment with UCB standards.
Prepare equipment and cages for weekly use.
Check animals on a daily basis and complete routine husbandry.
Be proactive, creative and innovative regarding housing, environmental enrichment, playtime and interaction for animals.
Provide the greatest care and respect for our animals.
Assisting/completing In-vivo experiments.
Liaising with scientists to ensure Animal Scientific Procedures Act (ASPA) is adhered to.
Assist in training other staff members.
Acting as a Named Animal Care & Welfare Officer (NACWO).

Interested? For this role we’re looking for the following education, experience and skills

Knowledge of Animals Scientific Procedures Act (ASPA).
Home Office License Holder PIL A-B.
NACWO qualifications or a willing to achieve
Experience of working with rodents and enthusiasm for animal welfare.
Competent in a variety of licensed procedures and a desire to continue learning.
Ability to commute to sites in both Slough and Windlesham.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Artwork & Packaging Development Expert (UK) (Slough, Berkshire, GB)

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We are looking for an Artwork & Packaging Development Expert who is detail driven, solution oriented, and creative to join our Devices, Artwork & Packaging team, supporting UCB’s global packaging network from early development through commercial lifecycle management, based in Braine-l’Alleud, Belgium or Slough, UK.

About the Role

As Artwork & Packaging Development Expert, you will lead the development and design validation activities for secondary and tertiary (transport) packaging solutions across UCB’s portfolio and global manufacturing and external partners’ network. Your scope will cover the full end-to-end lifecycle—from clinical development and human factors usability studies through submission, commercial launch, and lifecycle optimisation.

You will also play a central role in defining and evolving visual identity, graphic charters, and artwork solutions, translating design briefs into compliant, high-quality packaging and artwork files that support a wide range of business needs. In parallel, you will be responsible to strengthen processes, standards, governance, and continuous improvement across artwork and packaging development activities.

Who You’ll Work With

You will report to the Head of Artwork & Packaging Development and will be a central role as a recognized subject matter expert and key interface for the defined accountabilities.., for internal and external stakeholders across Manufacturing, Supply Chain, Artwork & Packaging Program Leadership, Packaging and Devices teams, Procurement, Marketing, Regulatory Affairs, and external design or manufacturing partners. You will collaborate in a global, cross functional environment to ensure packaging solutions are robust, scalable, compliant, fit for purpose, and sustainable (minimizing environmental impact, reducing waste, and promoting recyclability and efficient use of resources), in line with the UCB Global Artwork & Packaging Strategy concepts.

What You’ll Do

Within the Artwork & Packaging Program governance structure, you contribute with expert authority, among peer experts, with accountability for high‑quality development deliverables and activities (while Program Leads act as the central SPOC for cross‑functional oversight).
Lead secondary and tertiary packaging development projects from early concept to commercial launch through design validation, visual identity activities and industrialisation support. Clinical Trials packaging is part of the scope.
Drive development of innovative, manufacturable, and cost-effective packaging solutions that create patient, stakeholders and brand value.
Drive creation, evolution, and governance of visual identity, graphic charters, and artwork deliverables.
Ensure development processes, SOPs, and training materials are in place, followed, and continuously improved.
Identify packaging features that support patient usability, compliance, manufacturing efficiency, and supply chain reliability, cost consciousness
Support lifecycle optimisation initiatives, including cost of goods (COGs) improvement and packaging standardisation.
Provide technical expertise to packaging sites and partners, supporting troubleshooting, capacity optimisation, and technology transfer.
Understanding printing techniques and underlying impacts-constraints on branding-packaging development.
Contribute to the development and implementation of global packaging standards, guidelines, and design platforms and technical features.
Monitor external trends, technologies, regulations, and standards related to packaging and artwork, ensuring timely adoption and communication.
Support long-range manufacturing and packaging strategies, including risk assessment and mitigation planning.

Interested? For this role we’re looking for:

Strong communication skills with the ability to engage diverse technical and non-technical stakeholders.
Proactive, pragmatic, and solution-oriented working style, with the ability to manage multiple priorities.
Ability to influence, lead, and deliver results without direct authority.
Business proficiency in English.
Bachelor's or master's degree in engineering, packaging science, life sciences, or a related discipline.
5–10 years’ experience in packaging development within a GMP regulated pharmaceutical environment.
Solid project management experience in global, cross functional environments.
Demonstrated understanding of development activities related to secondary-tertiary packaging within manufacturing network across the end-to-end from clinical, human factors usability studies, submission into commercial launch and later lifecycle.
Strong knowledge of graphic design, visual identity creation, and regulatory labelling requirements.
Sustainability knowledge skills (understanding of materials, processes, and design strategies that minimize environmental impact, reduce waste, and promote recyclability and efficient use of resources).
Experience managing artwork development and external partners (design agencies, CMOs) is a strong advantage.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Data Science Lead 1 (Slough, Berkshire, GB)

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To strengthen our Global Advanced Analytics team, we are looking for an adaptable, collaborative individual with an intrapreneurial mindset for our Analytics Lead opening. This hybrid role is based in our headquarters in Slough, United Kingdom requiring 40% onsite presence and 5-10% international/ domestic travel.

About the role
You will help to inform on the commercial viability of various assets in development. You will be responsible for making exceptional business impact with the use of secondary data and insights development through advanced analytics methods, enabling an increased use of data and, where applicable, reducing the necessity for building primary data. You will also be responsible for managing and implementing advanced analytics/AI projects to ensure successful delivery. You will oversee the ongoing operations of advanced analytics solutions to ensure that models continue to work and scale them up with additional demand and applications. You will serve as the subject matter expert for Advanced Analytics/AI capabilities in support of business needs within Patient Solutions and Patient Evidence.

Who you’ll work with
You will co-create with Integrated Insights Leads from early asset and late stage (Phase 0-3) teams, Real world evidence teams, Translational Medicine and Bioinformatics, Clinical operations, clinical recruitment, and asset teams, new product planning teams, Commercial teams, Medical Affairs, Market Access, Finance, and IT. Externally, you will work with data and analytics vendors and partners.

What you’ll do

Analytics Leadership: Provide clear expertise for opportunities to leverage advanced analytics, especially where they are advantageous to reducing the need for primary data or have high marginal impact
Deliver the most impactful data and analytics projects that:

address the most compelling business questions, and/or
identify new opportunities for patients and UCB through effective visual displays of quantitative and qualitative information

Partnership and Collaboration: Be the key strategic partner for functional stakeholders and co-create plans and priorities for data and advanced analytics with them together with the Patient Solutions and Evidence Leads. Ensure tight relationships and collaboration with IT, Data Office, and other Analytics teams using relevant data sources.
Team Leadership. Serve as a mentor and guide to more junior data scientists and translators in demonstrating the application of cutting-edge analytics, clear communication and presentation of insights and practical/pragmatic implementation of key recommendations
Drive the execution of regional and local data-driven insights research and data analytics plans and priorities
Foster a strong data science community with significant business acumen and communication skills across Hubs and Engine and Supervise the conduct of advanced analytics studies in a collaborative manner ensuring that the study methodology is appropriate to deliver reliable results.
Improve the team’s partnership with, and impact on, key internal (UCB) and external stakeholders within the specific area of focus by:

developing and executing a communication and collaboration plan with key UCB stakeholders
increasing personal and the Advanced Analytics team’s knowledge of the business by ensuring that she/he and each team member has direct interaction with patients and/or other external stakeholders

Attract, retain, motivate, and develop key talent for the Advanced Analytics team; coach and develop team members
Drive deep partnership with the Hub insights team and other “fellow” Engines and insights generating functions (e.g. regional analytics teams) allowing for a joined delivery of cross-functional, deep impactful insights
Be a champion for a data-driven, decision-making culture

Interested? For this role we’re looking for the following education, experience and skills

Minimum Experience/Skills Required:

Bachelor's degree in quantitative area
Minimum of 8-10+ years experience applying predictive modeling techniques such as ML, decision trees, ensemble learning, neural networks etc, and data transformation such as data cleansing and integration, fuzzy matching, etc., is required
Minimum of 8-10+ years of experience developing program/project plans and leading programs/projects from initiation to implementation is required
At least 8 years of experience working with real world data (Claims data, EMR, IQVIA, -omics, etc)
Minimum of 8-10+ years of experience with programming and application development using Python or R is preferred

Preferred Experience/Skills:

Master/Doctor’s degree in quantitative area
Knowledge of pharmaceutical industry, ideally specialty pharma and biologic treatments
Deep expertise in leveraging data science methodologies within the Research and Development and Clinical trials sphere of the pharmaceutical industry. The Go-to-Market domain encompasses the commercial, medical, and market access facets of the business
Expertise in analyzing a range of large, secondary transactional databases, unstructured data or other computationally difficult challenges
You are a structured problem solver
Possess an 80/20 mindset to push for fast model iterations
Interpret model results and identify potential model errors (e.g., overfitting, model bias, correlation vs causation)
Global role, so willingness and flexibility to work across geographies / time zones (sometimes outside of core hours)

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Digital Technology Lead - Solution & Programs (Slough, Berkshire, GB)

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We are looking for a Digital Technology Lead - Solution & Programs who is passionate, collaborative, and curious to join our Digital Technology for Patient Solutions (DTPS) team, based in Slough office in the United Kingdom.

About the role

You will join DTPS, the IT group dedicated to Research and Early Development, to drive the modernization, integration, and optimization of laboratory technology ecosystems across Research & Early Development. As research becomes increasingly technology‑driven, you will support laboratory digitalization, automation, and AI‑enabled operations. Acting as a hybrid technical and business contributor, you will lead business analysis, process engineering, system implementation, and end‑to‑end project delivery. Your work will strengthen operational resilience, increase efficiency, and support strategic Digital Technology objectives in laboratory environments.

Who you’ll work with

You will collaborate in a multidisciplinary, international environment with scientists, laboratory end users, and operations teams. You’ll work closely with digital, data, and architecture teams, and external technology vendors. As part of the broader DTPS and IT community, you will act as a key connector between science, operations, and technology.

What you’ll do

Analyze, redesign, and optimize laboratory workflows, translating scientific and operational needs into functional and technical requirements
Lead or support mid‑size projects delivering laboratory systems, automation, and digital capabilities from planning through implementation
Act as IT System Owner for designated laboratory systems, ensuring lifecycle management, compliance, documentation, and audit readiness
Ensure system reliability, data integrity, cybersecurity alignment, and integration with scientific workflows
Support integration of automation, robotics, and AI‑enabled technologies within laboratory environments
Contribute to business cases, standardization, and continuous improvement of laboratory digital ecosystems

What we’re looking for

Master’s degree, PhD, or equivalent in a scientific, engineering, automation, or digital discipline
3+ years’ experience delivering digital technology, automation, or laboratory system projects
Demonstrated experience in business analysis, process design, or scientific workflow optimization
Strong understanding of laboratory environments, data flows, and instrument integration
Proven project management, stakeholder management, and cross‑functional collaboration skills
Curiosity for emerging technologies, particularly automation and AI in scientific contexts

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Non-Clinical Safety Lead - UK (Slough, Berkshire, GB)

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To strengthen our Non-Clinical Safety Evaluation group within Early Clinical Development and Translational Science, we are looking for a talented individual for the role of Non-Clinical Safety Lead, based in Braine L'alleud, Belgium or Slough, UK or Cambridge, MA (USA).

About the role

As a Non-clinical Safety Lead, you will provide scientific leadership for non-clinical safety across discovery and development programs. You will shape non-clinical strategies, ensure high-quality execution, and support regulatory interactions from early development through clinical progression and post approval. You will:

Lead, communicate, and execute non-clinical safety strategies aligned with clinical development goals.
Develop integrated non-clinical safety plans supporting innovative programs. Ensure timely delivery of high-quality non-clinical data and global regulatory documentation.
Represent UCB in interactions with regulatory authorities and external partners.

This role is well suited to an experienced toxicologist—ideally with exposure to gene and cell therapy or other novel modalities—who enjoys working at the interface of science, development strategy, and regulation. You will thrive in an environment where you can share expertise across functions and global UCB sites, engage with cutting-edge science and build collaborative networks to drive cross-functional success.

What you'll do

Provide non-clinical safety expertise to discovery and development projects
Define, lead, and implement non-clinical safety strategies across programs.
Partner with clinical teams to ensure robust preclinical data supports clinical trial design.
Contribute to global regulatory submissions (e.g., IBs, Briefing Books, INDs, NDA/BLAs) and interact with regulatory authorities.
Oversee the design, review, and interpretation of non-clinical studies.
Manage non-clinical safety programs, including budgets.

Interested? For this role you’ll need the following education, experience and skills

PhD in Toxicology, Pharmacology, or related discipline (or equivalent MS/DVM with experience).
5+ years in non-clinical safety (preferably in pharma or biotech).
Deep understanding of regulatory processes and regulatory toxicology.
Experience managing and forecasting non-clinical safety budgets.
Ability to produce high-quality reports and submission documents with subject matter expert support.

Preferred Qualifications:

Accredited or registered toxicologist.
Experience in gene and cell therapy and/or other novel modalities.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Clinical Development Lead (UK) (Slough, Berkshire, GB)

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We are looking for a Clinical Development Lead to join us in our Clinical Development team, based in any of our Brussels (Belgium), Monheim (Germany), Slough (UK) or Atlanta/Raleigh (US) offices.

About the role

As a Clinical Development Lead, you have the opportunity to leave a lasting impact on patients’ lives by driving innovative, patient-centric clinical strategies in a highly visible, high-stakes environment. Reporting to senior R&D leadership, you will lead the end-to-end design and execution of global development programs, working cross-functionally to translate science into access, and strategy into action.

Who you’ll work with

You’ll collaborate with global thought leaders, guide multifunctional teams, and influence decisions that shape both science and the business. You will report into the Global Head of Clinical Development for Immunology

What you’ll do

Set the global clinical development strategy for assigned asset(s), ensuring alignment with TPVP, regulatory requirements, and commercial goals.
Lead external engagement with global thought leaders, investigators, and stakeholders to continuously refine strategy based on emerging insights and unmet needs.
Design and adapt robust clinical development plans that integrate the latest scientific, regulatory, operational, and payer perspectives—balancing innovation with executional feasibility.
Oversee the execution of pivotal studies and regulatory submissions across all relevant markets, ensuring clinical excellence, data integrity, and timely delivery.
Shape clinical narratives and regulatory strategy, acting as a key representative in interactions with global health authorities and strategic partners.
Contribute to corporate strategy, supporting business development initiatives and representing the clinical perspective in asset evaluations.

Interested? For this position you’ll need the following education, experience and skills:

Advanced degree (MD, PhD, PharmD, or equivalent).
Track record of leading complex global programs across multiple indications.
Familiarity with digital health technologies, real-world data, and AI-enabled trial innovation.
Ability to lead through ambiguity, make informed decisions in uncertainty, and drive results across organizational boundaries.
Strategic mindset with a bias for innovation, speed, and operational excellence.
Exceptional communication and stakeholder management skills, including C-suite level.
Global experience and cultural fluency; willingness to travel internationally as needed.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Project Lead Programmer (UK) (Slough, Berkshire, GB)

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We are looking for a Senior Project Lead Programmer to join us in our Biometric & Data Science team, to be based in any of our Brussels (Belgium), Monheim (Germany), Slough (UK) or Raleigh (US) offices

About the role

The Senior Project Lead Programmer will drive the strategic development, governance, and execution of open-source initiatives within the Biometrics function. This role is central to advancing innovation in statistical programming, data science, and clinical analytics through open collaboration, transparent tooling, and community engagement. The position will work closely with Programming and Biostatistics teams to ensure open-source efforts are scientifically rigorous, regulatory-compliant, and operationally impactful. Provide strategic, technical, operating, and tactical transformation change and implementation of state-of-the-art programming and play a central leading role in the continuous transformation of the BDS organization at all levels: talent, capability build/needs, optimized and efficient operating model, initiatives, systems and strategy. Will optimize scoping, input, and solution provision through collaborations cross functionally.

Who you’ll work with

You will report into the Head of Programming Visualisation & Reporting

What you’ll do

Define and implement the programming team’s open-source innovation strategy aligned with the department goals.
Develop the vision and roadmap for open-source tools that directly support the Biometrics department, including programming, visualization, and reporting needs but not limited to.
Drive innovation in clinical trial analyses, using R to improve the efficiency of study results analysis delivery for the Programming team
Champion open-source principles across departments including R&D, IT, Regulatory Affairs, and Data Science.
Represent the company in external open-source consortia (e.g., Pharmaverse, PHUSE, etc.).
Responsible to lead high complex projects with multiple stakeholders (internal and external stakeholders) and articulated structure Lead and shape the continuous learning and upskilling culture for a modern Biometrics (Programming) organization

Interested? For this position you’ll need the following education, experience and skills:

MSc (preferred) in Statistics, Mathematical, Statistical Computer Science or Life Science, or equivalent
Deep understanding of open-source ecosystems, licensing models, and software development practices
Strong communication and stakeholder management skills across scientific and technical domains.
Experience with regulatory environments and data standards (e.g., CDISC, HL7).
Proficiency in platforms like GitHub and tools such as R, Python, Docker, and CI/CD pipelines.
Experience contributing to or leading open-source projects in clinical research or statistical programming.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Real World Evidence Expert (UK) (Slough, Berkshire, GB)

Make your mark for patients

We are looking for a Senior Real World Evidence Expert who is scientifically rigorous, strategically minded, and passionate about generating impactful real‑world evidence to help shape key decisions across the lifecycle of UCB’s assets, based in Slough, UK or Brussels, Belgium

About the Role

As a Senior RWE Expert, you will autonomously design, lead, and deliver a wide range of global real‑world evidence (RWE) studies. Your work will inform internal decision-making, support regulatory and payer interactions, and contribute to the scientific understanding of disease areas. In addition to overseeing project delivery, you will help shape asset‑level RWE strategies and propose innovative approaches to evidence generation in partnership with the RWE Strategy Lead.

Who You’ll Work With

You will collaborate with statistical teams, RWE Analysts, epidemiologists, clinical teams, Evidence Synthesis partners (HE/HTA), Safety/Pharmacovigilance, external vendors, medical experts, and cross‑functional asset teams. You will serve as an influential scientific contributor with the ability to engage diverse stakeholders and ensure RWE outputs meet strategic, regulatory, and scientific needs.

What You’ll Do

Lead execution of complex global RWE studies using diverse methodologies and datasets end‑to‑end.
Develop study concepts, write protocols, shape analysis plans, and ensure governance and QC compliance.
Deliver epidemiology, natural‑history, burden‑of‑disease, safety‑outcome, regulatory, and comparative‑effectiveness studies.
Represent RWE on primary data‑collection teams and lead high‑visibility secondary data‑use initiatives.
Collaborate with vendors, clinicians, statisticians, and analytics teams to deliver scientifically robust outputs.
Interpret results and communicate findings internally and externally across scientific and strategic forums.
Co‑define evidence needs with HE/HTA partners, Safety, and other functions to support regulatory and payer interactions.
Contribute to asset‑level RWE strategy and propose innovative study designs, data sources, and analytic approaches.
Advocate for rigorous scientific methodology and challenge assumptions using strong methodological reasoning.
Help advance RWE functional excellence through thought leadership, innovation, and best‑practice sharing.

Interested? For this role we’re looking for:

Master’s degree, PhD, or MD in a life science, epidemiology, outcomes research, HEOR, statistics, or related field.
Experience designing and delivering RWE studies using primary or secondary data in pharma, academia, or consultancies.
Strong quantitative and methodological expertise across epidemiology, pharmacoepidemiology, and outcomes research.
Ability to develop high‑quality scientific communications (abstracts, manuscripts, posters, presentations).
Excellent communication skills with the ability to influence and engage cross‑functional and senior stakeholders.
Proven ability to lead projects independently, think strategically, innovate, and adapt in fast‑changing environments.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Healthcare & Access Partner - Dermatology - North London (Slough, Berkshire, GB)

Make your mark for patients

We are looking for a Healthcare & Access Partner to join us in our UK & Ireland Dermatology team, to be field based covering North London

About the role

Amplifies and strengthens the matching of UCB therapeutic options with appropriate patients in assigned accounts and territory through strong collaborative relationships with key healthcare professionals

Who you’ll work with

You will report into the Ecosystem Lead – South for our Dermatology franchise

What you’ll do

Acts as single point of contact for healthcare professionals by applying deep knowledge of UCB solutions and connecting the right resource at the right time
Tailors omni-channel tools to impact healthcare professionals based on individual preferences
Defines and executes an impactful tactical plan within territory of responsibility
Be an efficient point of contact to independent healthcare professionals supporting them to provide optimal care
As part of a multidisciplinary team coordinate stakeholder management in a community-based environment through two-way interactions with healthcare professionals helping them to provide optimal care
Establish strong business relationships with healthcare professionals within assigned territory
Matching of UCB therapeutic options via a deeper understanding of targeted healthcare professionals patient population by deploying a tailored approach (communication and tools) and solutions

Interested? For this position you’ll need the following education, experience and skills:

Bachelor’s degree required
Previous pharmaceutical or health care management experience e.g. ABPI examination.
A successful track record in key account/project management and influencing key health care customers.
Experience and knowledge of relevant disease areas i.e. Dermatology, Immunology, etc.
Demonstratable National and sub-national NHS knowledge plus in-depth disease, market and competitive intelligence expertise.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Principal Statistician (UK) (Slough, Berkshire, GB)

Make your mark for patients

We are looking for a Senior Principal Statistician to join us in our Biometrics & Data Science team, based in any of our Brussels (Belgium), Monheim (Germany) or Slough (UK) offices.

About the role

You will lead as the strong voice for Early Development Statistics, helping drive the development of UCB compounds, providing statistical expertise in technical areas such as clinical pharmacology, pre-clinical statistics and or biomarker strategy and bioassay development.

Who you’ll work with

You will report into the Head of Early Development Statistics or a technical area leader in her team (Translational Statistics lead, or Clinical Pharmacology Statistics Lead)

What you’ll do

Provide direction and continuous leadership of the Early Development Statistics team – for compounds under development, via an expert area such as clinical pharmacology statistics, pre-clinical, biomarker and or bioassay development.
Lead and influence the translation of strategy to tactical planning, operations, and quality
Contribute to strategic planning of the non-clinical and or clinical development plan, including study designs, design of experiments, analysis plans, quantitative decision criteria, exploratory analysis etc.
May oversee more junior statisticians, to ensure operational delivery of statistical outputs, for clinical or non-clinical studies.
Work closely with relevant stakeholders in the team, such as research lead, biomarker lead, bioassay development lead or quantitative clinical pharmacology lead, in alignment with statistics leaders such as Project Lead Statistician, translational statistician, or clinical pharmacology statistician.
Help lead the continuous learning and upskilling culture for a modern Biometrics (statistics) organization

Interested? For this position you’ll need the following education, experience and skills:

MSc. Or Ph.D. in Biostatistics or Statistics, or equivalent
More than 5 years in the pharmaceutical industry;
Solid knowledge of drug development across all phases.
Experience in Early Development, in at least one technical area (pre-clinical, translational (biomarker/bioassay), or clinical-pharmacology)
Understands how the functional expertise and contributions fit into the bigger picture
Influencer and collaborator in a development team environment
Good communication skills
Programming skills in R or SAS

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

EU Evidence Generation Lead - Rare Diseases & Epilepsy (Slough, Berkshire, GB)

Make your mark for patients

We are looking for an EU Evidence Generation Lead Developmental Epileptic Encephalopathies and Epilepsy who is strategic, collaborative, and highly self-driven to join us in our Rare Diseases & Epilepsy team, based in Slough, UK.

About the role

You will lead and execute evidence generation strategies across Europe to support patient access and the differentiation of our therapies for developmental epileptic encephalopathies and epilepsy. This highly external-facing role ensures robust, impactful projects and maximizes the visibility of our evidence generation activities.

Who you’ll work with

You will collaborate closely with EU country medical teams, global colleagues, and external partners. You’ll engage with key opinion leaders, regulatory bodies, and cross-functional teams to deliver on strategic objectives in a matrix organization.

What you’ll do

Build and maintain strong relationships with external partners and EU country teams
Oversee development and execution of evidence generation plans in key markets
Drive delivery of EU-level projects, ensuring timelines, budgets, and quality standards
Represent UCB at scientific forums and with regulatory and reimbursement bodies
Champion innovative digital solutions to enhance evidence generation
Lead capability building and training for EU teams
Collaborate across matrix teams and work independently to achieve objectives

Interested? For this role we’re looking for the following education, experience and skills

Bachelor’s degree with relevant professional experience required; Master’s or PhD preferred
5+ years’ experience in evidence generation, preferably in epilepsy or rare diseases
Proven ability to thrive in a complex matrix organization
Demonstrated team player with excellent collaboration skills, yet highly self-driven and able to work independently
Strong understanding of healthcare ecosystems and policy shaping
Excellent communication and relationship-building skills
Digital literacy and agile mindset

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Pharmacometrics Team Lead (UK) (Slough, Berkshire, GB)

Make your mark for patients

We are looking for a Pharmacometrics Lead, who is innovative and agile to strengthen our Quantitative Clinical Pharmacology group, based at our research site in Slough (UK), Monheim (Germany) or Braine (Belgium).

About the role

Bringing experience in the application of pharmacometrics to pediatric drug development, Neurology and Immunology, with the aspiration to lead/manage more junior staff, to contribute to the teams’ development and grow expertise and skills in these areas.

Who you’ll work with

Reporting to the Global Head of Pharmacometrics, you’ll be leading a team of Pharmacometricians, from both a technical and scientific perspective, to ensure state of the art pharmacometrics approaches are applied to optimize drug discovery and development.

Working closely with the QCP Leads assigned to the various projects, to ensure clear integration of the pharmacometrics aspects into the programs.

What you’ll do

Coaching and mentoring junior staff on how to navigate within a project and matrix organization.
Leading and delivering the Pharmacometrics strategy to support development of our assets. extrapolation (where appropriate), dose selection, trial design, PIP development and ongoing evaluation of data as generated.
Performing hands-on population PK/PD, exposure-response modeling and clinical trial simulations on an assigned project.
Developing submission ready fit for purpose Pharmacometrics analysis plans and reports.
Initiating and overseeing outsourced pharmacometrics activities and further internalizing the work as needed.
Having a working knowledge about the regulatory pathways on a global basis and opportunities for collaboration with health authorities (either through working parties, advice meetings, and other initiatives) in pediatrics, Neurology and Immunology.
Promoting MID3 internally and externally.

Interested? For this role you’ll need the following education, experience and skills

Doctorate (PhD or MD) in the related disciplines of Pharmaceutical Sciences, Statistics or Engineering.
8+ years (Bio)pharmaceutical industry experience in Pharmacometrics with minimum of 2 years line management responsibilities.
Hands-on experience in population PK/PD, disease progression modeling, and clinical trial simulations.
Strong understanding and knowledge of Bayesian methodologies, model-based meta-analyses, PBPK, QSP, and AI/ML in Pharmacometrics.
Expertise in R, NONMEM or related pharmacometrics software.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Clinical Development Lead (Tokyo, Tokyo, JP)

Make your mark for patients

患者さんのためにあなたの力を発揮してください

私たちは、情熱的で、成長志向があり、戦略的思考力のあるクリニカル・ディベロップメント・リードを募集しています。東京に拠点を置く臨床開発チームの一員として、担当製品の日本における臨床開発戦略の立案と実行をリードしていただきます。社内外のステークホルダーと連携しながら、規制当局対応、申請書類作成、外部専門家とのネットワーク構築などを通じて、製品の成功に貢献する役割です。

【チームについて】
あなたは、臨床開発、メディカルアフェアーズ、薬事、ファーマコビジランス、マーケティングなどの社内関係者と密接に連携しながら、日本の臨床開発戦略を推進するチームで働くことになります。グローバルアセットチームや関連部門とも協働し、日本の視点を反映した開発計画を策定・実行します。

【主な業務内容】
・日本における臨床開発計画の立案と実行
・規制当局との対応および申請書類の作成支援・外部専門家とのネットワーク構築と関係維持
・臨床試験の設計、実施、評価、報告の監督
・社内外ステークホルダーへの戦略説明と調整
・薬事申請、承認、上市に向けた臨床面での貢献

【応募資格】
・ライフサイエンスまたはヘルスケア分野の学士号（修士号、Ph.D.、M.D.、PharmD尚可）
・製薬業界での臨床開発経験5年以上・複数の臨床試験の同時進行管理経験
・規制当局との対応経験および申請書類作成経験
・日本語および英語での優れたコミュニケーション能力
・戦略的思考力と問題解決能力
・マトリックス環境でのチームリーダーシップ経験

【応募方法】
・日本語と英語の履歴書を1つのファイルにまとめ、システムにアップロードしてください
・UCB社員からの紹介がある場合は、応募時にその旨をシステム上でご記載ください

担当リクルーター：河合

患者さんのために価値を創造し、ご自身の力を発揮する準備ができているとお感じでしたら、ぜひ私たちにご連絡ください。

会社概要

UCBは、神経および免疫領域に注力するグローバルなバイオ医薬品企業です。世界中で約8,500人の社員が、患者さんからインスピレーションを受け、科学の力で前進しています。

UCBで働く魅力

UCBでは、単に業務をこなすのではなく、価値を創造することを大切にしています。私たちは挑戦を恐れず、協力し合い、革新を追求しながら、患者さんのために成果を出すことを目指しています。
誰もが尊重され、受け入れられ、最善を尽くせる平等な機会がある、思いやりと支援に満ちた文化が根付いています。
私たちは常に「その先」を目指し、患者さん、社員、そして地球に対して人間らしさを大切にした価値を提供しています。UCBで働くことで、自分自身の成長を実感し、自由にキャリアを築き、可能性を最大限に引き出すことができます。

UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。

選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください：

EMEA-Reasonable_Accommodation@ucb.com

※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。

障がい者採用開発本部事務職（薬事もしくはオペレーション部） (Tokyo, Tokyo, JP)

患者さんのためにあなたの力を発揮してください

主な業務内容について

下記２事業部のどちらかの配属を想定しております。
知識・経験により具体的な業務内容は調整可能です。

【薬事部】
・薬事部の過去の電子書類のアーカイブ整理やデータ入力
・申請システムのメンテナンスやアップデート対応
・提出書類のマスキング対応など

【オペレーション部】
・契約書類のアーカイブ整理
・監査対応のための書類整理
・ドキュメントリストの作成など

応募資格・スキル

・PCの正確な操作が出来る方

（尚可）
・英語を使っての勤務経験のある方

担当リクルーター：堀口

※フルリモート不可/Hybrid work model

※Please check if the candidate has applied for a job at UCB in the past year.　一年以内のご応募歴を必ずご確認ください。

※Please make resume combined in one document to submit　書類を一つに纏めてご提出ください。

※If you have any questions, please contact recruiting team 質問がございましたら採用チームまでお問い合わせください

患者さんのために価値を創造し、あなたの力を発揮して「その先」に進む準備はできていますか？もしそう思われるなら、ぜひご応募ください！

UCBについて
UCBは神経学と免疫学に特化したグローバルなバイオ医薬品企業です。UCBは、世界各地に約8,500人の従業員を擁し、患者さんに触発され、科学を原動力としています。

UCBで働く理由
UCBでは、単に仕事をこなすだけでなく、価値を創造します。私たちは、患者さんのために前進し、協力し、革新することを恐れません。UCBには、思いやりがあり、協力的な社風があります。そこでは、誰もが仲間とともに尊重され、ベストを尽くす機会を公平に与えられています。私たちは、患者さん、従業員、地球のいずれに対しても、常に人間的な視点に立ち、患者さんのために価値を創造する「その先」を目指します。UCBで働けば、自分が成長できる場所を発見し、自分の可能性を最大限に発揮するために自分のキャリアパスを切り開く自由を得ることができます。

UCBにおけるサステナビリティと、それが私たちのビジネスアプローチにどのように統合されているかについては、こちらをご覧ください。

UCBとその子会社は、職場における多様性と包括性を奨励しています。人種／肌の色／宗教／性別／国籍／退役軍人／障害／年齢／性的指向／性自認による差別は行いません。

あなたの強みや能力を発揮するために、日本での職種への応募に特別な配慮が必要な場合は、Ucb_recruit@ucb.com までご連絡ください。その他のお問い合わせの場合、このルートではサポートできませんのでご注意ください。

Principal Statistician (Tokyo, Tokyo, JP)

Make your mark for patients

(English Follows Japanese)

【チームについて】
あなたが所属するチームは、グローバルおよび東アジア地域の臨床開発を支えるバイオメトリクス＆データサイエンス部門です。国内外の多様な専門家と協力し、革新的な統計解析やデータサイエンスの手法を用いて、グローバルレベルでの医薬品開発の質と効率向上に貢献しています。患者さんにとっての価値を創造するため、チームは常に新しい知識やスキルの習得を重視し、協働と成長を促進する環境です。
【主な業務内容】
・開発化合物に対し、バイオメトリクス＆データサイエンス部門の代表として、統計的観点からの開発戦略を含むプログラム全体を支援する
・統計関連の成果物に対する責任をもち、国内外のプロジェクトチームの意思決定に寄与する
・バイオメトリクス＆データサイエンス部門の継続的なイノベーションとスキル向上の文化醸成に貢献する
・社内外で部門の代表として活動し、業界をリードしながら、組織の評判向上に寄与する
・医薬品開発におけるトレンド（RWDの活用、Complex innovative design等）を把握し、戦略の提案・実行につなげる
・統計担当者の立場から申請準備や規制当局とのやり取りを行い、承認取得に貢献する
【応募資格】
・統計学または生物統計学分野の修士号または博士号
・臨床試験の統計担当者として6年以上の実務経験
・少なくとも1つの規制当局（例：FDA、EMA、PMDA、CDEなど）への申請および承認経験
・国内外のステークホルダーとの調整・交渉をおこなえる優れた書面および口頭でのコミュニケーション力
・最新の統計手法に関する議論に対応できる柔軟性および専門性
・自発的に行動し、戦略から実務まで遂行できる実行力
・統計プログラミング言語（例：SAS、R）およびサンプルサイズやシミュレーションソフト（例：EAST、nQuery、WinBugsなど）に精通
・プログラマーと協業するためのCDISC標準（SDTM/ADaM）に関する知識
・チームリーダー経験（例：統計チーム（またはプログラミングチーム）のマネジメント経験）があれば尚可
【応募方法】
・日本語と英語の履歴書を1つのファイルにまとめ、当社システムにアップロードしてください
・UCB社員からの紹介や知人がいる場合は、応募時にシステム上でその旨を記載してください

ーーーーーーーーーーーーーーーーーーーー

【About Our Team】

You will be part of the Biometrics & Data Sciences (BDS) department, which supports global clinical development. By collaborating with diverse experts both within Japan and internationally, our team leverages innovative statistical and data science methodologies to enhance the quality and efficiency of drug development on a global scale. With a strong focus on creating value for patients, our team emphasizes continuous learning of new knowledge and skills, fostering an environment that promotes collaboration and growth.

【Key Responsibilities】

Serve as a representative of the Biometrics & Data Sciences department for development compounds, supporting the overall program including development strategies from a statistical perspective.
Take accountability for statistical deliverables and contribute to decision-making within domestic and global project teams.
Contribute to fostering a culture of continuous innovation and skill development within the Biometrics & Data Sciences department.
Act as a representative of the department internally and externally, helping strengthen the organization’s reputation while taking a leadership role within the industry.
Stay abreast of trends in drug development (e.g., use of RWD, complex innovative designs) and propose and implement strategies accordingly.
Support submission preparation and interactions with regulatory authorities from the statistical perspective, contributing to successful approvals.

【Qualifications】

Master’s or Ph.D. in Statistics or Biostatistics.
At least 6 years of hands-on experience as a statistician in clinical trials.
Proven experience in submissions and approvals with at least one regulatory authority (e.g., FDA, EMA, PMDA, CDE).
Excellent written and verbal communication skills with the ability to coordinate and negotiate with stakeholders across countries.
Flexibility and expertise to engage in discussions on the latest statistical methodologies.
Proactive attitude with the ability to execute from strategy through to operations.
Proficiency in statistical programming languages (e.g., SAS, R) and sample size/simulation software (e.g., EAST, nQuery, WinBUGS).
Knowledge of CDISC standards (SDTM/ADaM) for effective collaboration with programmers.
Team leadership experience (e.g., managing a statistics or programming team) is a plus.

【How to Apply】

Please combine your resume in both Japanese and English into a single file and upload it to our application system.
If you have been referred by a UCB employee or have contacts within the company, please indicate this information in the system at the time of application.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Patient Access Partner Korea (Seoul, Seoul, KR)

Make your mark for patients

[Patient Access Partner Korea]

We are looking for a Patient Access Partner Korea to join us in our Market Access & External Engagement team, based in Korea.

About the role

Support to achieve and maintain the optimal pricing and reimbursement of the UCB products to align with the business strategy
- New Drug Listing & Indication expansion Strategy and management of UCB Products
Post listing management alinged with product strategy.
Evidence developement and execute evidence generation to demonstrate the value of UCB products brings to the patients.
Enhance Relationships with key government officials and hospital listing bodies as well as UCB internal stakeholders to shape favourable environment for patients‘ access.
Foresee the health policy and environmental chances and provide up-to-date market access intelligence to support more predictable business planning and patient’s benefit
Provide P&R support to all areas of the business, according to departmental priorities and principles
Support external engagements to deliver the value of UCB’s products and improve patients‘ access to the innovative UCB’s products.

What you’ll do

New Drug Listing & Indication expansion Strategy/Management of UCB Products

Develop and identify reimbursement strategies for new products and new indications to support optimal NHI listing and pricing
Conduct early assessment of products and initiate activities for reimbursement success
Write and review of National P&MA applications in view of a submission to payers
Present to/negotiate with payer/HTA body
Manage the timeline and quality of reimbursement projects (High quality BNHI submissions, P&R Document, PE Report, PE study, etc.)
Identify, engage and co-ordinate the external resources where required
Develop negotiation strategies and manage negotiation prices to optimize NHI listing and pricing, or minimize business impact

Post Listing Management
- Manage reimbursement status and reimbursement criteria, NHI price
- Develop and identify PVA strategy and manage PVA
- Negotiate NHI price
Evidence generation
- Plan local evidence generation for payer communication and execute it.
Relationships with Government officials and target stakeholders

Foster strong working relationships with Government officials(reviewers and PBRS members) and hospital listing bodies
Use key relationships with target stakeholders to facilitate optimal relationships with Government

- Provide /educate in-house customers
- Communicate and manage health care professionals & medical experts for responsible projects
- Maintain relationships and negotiate contracts and prices in accordance with the overall sales
- Analyze and determine the most important account in an organization at any time
- Shape the pricing related regulatory environment by actively participating in the industry-government discussions
Operational pricing
- Manage the approval of price change or launch, thru approval of Biz case
External engagement
- Support external engagments to deliver the value of UCB’s products and improve patients‘ access to the innovative UCB’s products.
- Develop external engagements plan and execute with the relavant stakeholders.
Keep the KR pricing data in the global pricing database updated timely

Interested? For this role we’re looking for the following education, experience and skills

Experience (List the type and length of experience)

Minimum 3 years’ experience in MNC pharmaceutical company
More than 3 years’ experience in pricing & reimbursement
Management of all product life cycle is preferred (e.g. filing experience for new drug listing and/or reimbursement expansion)
RSA or PE exemption/Rare disease experience prefered

Specific skills (Include specific skills and knowledge necessary to meet the objectives of the position)

Strong interpersonal & Good communication skill
Negotiation and facilitation skills
Strategic focus
Good knowledge in pharmaco-economics
Knowledge of relevant legislation
Knowledge of relevant professional standards and best practices
Understanding of medical background and Clinical Trial Data analysis & evaluation
Good command of Budget Impact Analysis between business impacts.

Understanding of global P&R approach and process Advanced skill/competency in recognizing, analysing and solving problems
Excellent English in speaking and writing

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

障がい者採用 Medical Strategy Associate（担当疾患領域：てんかん） (Tokyo, Tokyo, JP)

患者さんのためにあなたの力を発揮してください

職務概要

てんかん領域における患者さんや医師の声、ならびに最新の科学的知見を収集・整理し、メディカルアフェアーズ部の活動（戦略検討、情報提供、エビデンス創出等）に活用する業務に関わっていただきます。

仕事内容

以下の業務について、まずはマネージャー、既存メンバーのサポート業務からスタートしていただき、適性や習熟度に応じて、徐々に業務をお任せしていく予定です。
・てんかん領域の患者さんや医師からの意見を、今後のメディカルアフェアーズ活動を検討する上で重要な「気づき（インサイト）」として整理する。
・てんかん領域に関する論文や学術情報を収集し、スライド等の資料にまとめる。・社内外の関係者との会議設定、議事録作成、ならびに関連文書の作成・管理を行う。
・講演会の企画実行（年7～８回）

応募条件

【必要な経験・スキル】
・大学理系学部卒業、又は相応のサイエンスバックグラウンド
・日本語および英語の論文を理解できる方・PCの基本的なアプリケーション（Microsoft Outlook、Word、PowerPoint、Excel）を使用できる方

【あれば尚可】
・生成AIを活用した情報整理や資料作成の経験がある方

担当リクルーター：堀口

※フルリモート不可
※日本語の履歴書と職経歴書を１つのファイルに纏めてアップロードしてください
※ご不明点、ご質問がございましたら採用チームまでお問合せください。

患者さんのために価値を創造し、あなたの力を発揮して「その先」に進む準備はできていますか？もしそう思われるなら、ぜひご応募ください！

UCBにおけるサステナビリティと、それが私たちのビジネスアプローチにどのように統合されているかについては、こちらをご覧ください。

Investigations Lead APAC (Tokyo, Tokyo, JP)

Make your mark for patients

Investigations Lead APAC (English Follows)

私たちは、倫理調査リードとして活躍でき、「誠実さを大切にし、状況に柔軟に対応し、多文化環境で力を発揮できる」方を募集しています。勤務先は、東京オフィスの Ethics & Integrity チームです。

We are looking for an Investigations Lead, Asia Pacific who is curious, principled, and collaborative to join our Ethics & Legal Affairs team, based in our UCB Japan office in Tokyo, Japan.

About the role（職務概要）

このポジションでは、組織の信頼性を守るために、不正や不適切行為が疑われる案件の調査を公平かつ迅速に実施します。調査で得た気づきを基に、予防策の強化や倫理文化の促進にも貢献します。日本を中心にアジア太平洋地域の関係者と連携し、透明性・説明責任・倫理性の向上を支える役割です。

You will be working in a team that protects the organisation’s integrity by leading fair, timely, and robust investigations across the Asia Pacific region. You will provide insight that strengthens ethical culture, improves compliance processes, and reduces organisational risk. You will partner across multiple countries to ensure accountability, transparency, and learning.

Who you’ll work with（関わるチーム）

You will be working in a team that 倫理・法務の専門家で構成され、地域各国のビジネスリーダー、人事、内部統制、リスク管理など多様な部門と協働します。
互いに支え合いながら、組織の倫理文化を強化する国際的で協力的なチームです。

You will be working in a team that collaborates closely with colleagues across Ethics & Legal Affairs, People & Culture, business leaders, and local affiliates in Asia Pacific. You will also interact with employees across a variety of functions to gather information, share learnings, and support a strong ethics and compliance mindset.

What you’ll do（主な業務内容）

報告案件を評価し、調査または事案分類を適切に判断
公平で徹底した調査を内部ガバナンスに沿って実施
関係者へのインタビューと事実確認を効果的に実施
是正措置・再発防止策・必要な処分のフォローアップ
調査から得た知見を共有し、倫理文化向上を支援
調査関連の方針や手順の整備・改善を継続的に推進
Lead investigations to ensure fairness, accuracy, and timely resolution· Assess incoming matters and determine appropriate investigation pathways
Conduct interviews and gather information to establish reliable findings
Oversee corrective and preventive actions following investigations
Identify legal or ethical risks and recommend mitigating actions
Maintain organised, accurate documentation for all investigation activities

Interested? （求める経験・スキル）

製薬業界での実務経験（3年以上）
医療領域のコンプライアンスに関する知識と経験
日本語ネイティブレベルの運用能力
英語での優れた文書作成力とコミュニケーション力
多文化・多国籍の環境での協働経験
人事領域での調査経験
Experience in the pharmaceutical or healthcare industry
Experience in compliance or investigations roles
Ability to work effectively in multicultural, international environments
Strong communication skills in Japanese and English
Ability to identify risks, analyse root causes, and propose solutions
Skilled at conducting interviews and evaluating information objectively

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Planning & Execution Lead Immunology (Tokyo, Tokyo, JP)

Make your mark for patients

患者さんのためにあなたの力を発揮してください

Major Responsibilities
The role of PE Lead is to work with PVU/Franchise Head to create a system for ensuring the most effective and efficient Business operation (Commercial & Medical) through better alignment among Solutions, Medical, and Sales teams as well as other business and support functions.
In order to fulfill this role, the PE Lead is responsible for the following.

Business Operation Management:
Serve as a hub for each brand and indication and ensure efficient and effective business (Commercial & Medical）activities based on the PVU/Franchise’s portfolio strategy.
 Collaborates with various functions and lead the creation of resource plans and co-create training plans with L&D for PVU/Franchise
 Identify the operational issues in coordination with Solutions, Sales and Medical teams and propose solutions to PVU/Franchise Head
 Collaborates with I2I and SOM to conduct monthly analysis of the PVU/Franchise sales performance, landing forecasts, and business progress including field execution results, and lead regular business reviews.

Project Management (within PVU/Franchise)
 Lead the planning and execution of various priorities and new ideas within PVU/Franchise on a project basis, and align with other business/functions.
 Lead the execution of new cross-PVU business projects such as AI and digital projects in PVU/Franchise, in collaboration with Solutions and Strategic Operations teams.

Business Planning
Serves as the hub of information gathering and consolidation in the process of PVU/Franchise budgeting, FCASTx, and LRF to support PVU/Franchise Head.

Change Management
Collect various types of feedback in PVU/Franchise on a regular basis and leads the creation of a system to foster and maintain engagement and momentum.

Chief of Staff for PVU/Franchise Head
Event/meeting scheduling etc,.to be defined by each PVU/Franchise

ストラテジスト職責

主な職務内容
ストラテジストの役割は、PVU/Franchiseヘッドと協力し、ソリューション、メディカル、セールス、その他のビジネスおよびサポート部門間の連携を強化することで、最も効果的かつ効率的なビジネスオペレーションを実現するシステムを構築すること。この役割を果たすために、ストラテジストは以下の責任がある。

事業運営管理（営業企画的な仕事）：
各ブランドおよび適応症のハブとなり、PVU/Franchiseのポートフォリオ戦略に基づき、PVU/Franchise内の効率的かつ効果的なビジネス活動（Commercial & Medical）をリードする。
 様々な部署と連携し、PVU/フランチャイズのリソースプランの作成をリード、L&Dと共同でトレーニングプランを作成する。
 ソリューション、セールス、メディカルチームと連携して業務上の問題を特定し、PVU/Franchiseヘッドに解決策を提案する。
 I2IやSOMと協力し、PVU/フランチャイズの販売実績、着地予測、フィールド活動成果を含めた事業進捗の月次分析を行い、定期的なビジネスレビューをリードする。

プロジェクトマネジメント（PVU/フランチャイズ内）
 事業部内の様々な優先事項や新しいアイデアの計画と実行をプロジェクトベースでリードし、他の事業部/部門との連携を図る。
 ソリューションチームやストラテジックオペレーションチームと連携し、PVU/フランチャイズにおけるAIやデジタルプロジェクトなど、PVU横断的な新規ビジネスプロジェクトのPVU/Franchise内での実行をリードする。

ビジネスプランニング
PVU/Franchiseのバジェット、FCASTx、LRFプロセスのPVU/Franchise内での情報収集、Consolidationのハブとなり、PVU/Franchise Headをサポートする。

チェンジマネージメント
PVU/Franchise内の様々なフィードバックを定期的に収集し、PVU/Franchise全体のエンゲージメントとモメンタムを醸成・維持するためのシステム作りをリードする。

PVU/フランチャイズヘッドのチーフスタッフ
イベント/ミーティングのスケジューリングなど、各PVU/Franchise内にて定義する

患者さんのために価値を創造し、ご自身の力を発揮する準備ができているとお感じでしたら、ぜひ私たちにご連絡ください。

会社概要

UCBで働く魅力

UCBでは、単に業務をこなすのではなく、価値を創造することを大切にしています。私たちは挑戦を恐れず、協力し合い、革新を追求しながら、患者さんのために成果を出すことを目指しています。
誰もが尊重され、受け入れられ、最善を尽くせる平等な機会がある、思いやりと支援に満ちた文化が根付いています。
私たちは常に「その先」を目指し、患者さん、社員、そして地球に対して人間らしさを大切にした価値を提供しています。
UCBで働くことで、自分自身の成長を実感し、自由にキャリアを築き、可能性を最大限に引き出すことができます。

UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。

選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください：

EMEA-Reasonable_Accommodation@ucb.com

※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。

Supply chain specialist (Hong Kong, Hong Kong, HK)

Make your mark for patients

[Hong Kong Supply Chain Specialist]

We are looking for a Hong Kong Supply Chain Specialist to join us in our IC Market Supply Operations team, based in our Hong Kong office

About the role

This position is primarily accountable for maximizing Supply Chain performance in Hong Kong. Achieving target service levels, improving cost-to-serve and delivery of key product launches are the success criteria in meeting market needs.

This position must set direction for local supply chain that is aligned with global strategy, create and maintain effective relationships with local commercial leadership and ensure strict compliance with internal standards as well as external regulations.

Key responsibilities include: building competency and expertise, implementing 'best-practice' core SCM processes (i.e., demand forecasting, SIOP/demand meetings), ensuring transparent and rapid flow of critical issues/risks to key Global Supply Chain stakeholders, continuous improvement/optimization of network performance (i.e., working capital levels, distribution costs), active engagement in risk-management efforts to mitigate supply interruptions/losses and effective management and delivery of key projects/initiatives. This position is primarily accountable for maximizing Supply Chain performance in

Hong Kong. Achieving target service levels, improving cost-to-serve and delivery of key product launches are the critical success criteria in meeting market needs.

What you’ll do

Demand Management

Develop forecasting excellence adding local market expertise and ensuring local business alignment via regular SIOP / IBP meetings with appropriate local stakeholders: Sales, Marketing, Regulatory, Finance, QA…
Maintain UCB forecasting tool considering monthly collaboration calendar set at Global level
Coordinate Supply Chain aspects of phase in – phase out products, new product launches (incl. support to business case submissions and transfer price requests), (early) patients’ programs or tenders

2- Inventory Management

Ensure local inventory management process is implemented according to group policy and rules (safety stock, material review board process…)
Manage and control inventory to secure an appropriate stock level in the country and consequently, prevent out of stock situations or excessive inventory
Coordinate import/export transactions and release of products (temp loggers, deviations, release…)
Support recall activities of products from the market, together with Global Supply Chain, local QA, local RA, local Business.
Coordinate write-offs

3- Local Vendor Relationships Management

Manage local vendors (“3PL, Customs broker”) according to guidance provided by UCB External Network Governance, by acting as External network Vendor Manager and ensuring that service is compliant with agreements in place
Collaborate to negotiation and update of business agreements
Manage risk assessment for local vendors and ensure that any required corrective/preventive actions are implemented in a timely manner
Evaluate and implement improvement and cost reduction initiatives
Review and control of 3rd party providers’ invoices

4- Systems & Global Tools

SAP SD module: As local Key User (LKU) daily monitoring of the 3PL interface reports, follow new product codes creation
Perform, contribute to monthly SAP closing activities & any local reporting needed
Coordinate the relationship between Global IT, Global Key User (GKU) and 3PL to reach system fixing or processes amendments if/when needed
Maintain vendor’s and customer’s details updated and make sure they match in SAP
Ensure business continuity

5- GMP/GDP Compliance Management

Support Quality and ensure compliance (new GDP, falsified medicines…)
Ensure UCB Affiliate and partners (“3PL, Customs broker”) comply with all GMP/GDP Regulations
Creation/updating of SOPs of the area

6- Reporting and KPI

Prepare or/and monitor internal KPIs (product availability, days out of stock, obsoletes, OTIF, forecasting accuracy…) and report to group (timely-correct and complete)
Identify improvement opportunities in the areas of quality, cost, and service for the local SC function

7- Projects

Support local projects (Business development, reporting to Authorities…) on top of global (Supply Chain, Tax, Business development…) ones

8- Others

Manage Customer Service/O2C activities/Tenders management
Taking part in the management and resolution of complaints and deviation cases
Manage day-to-day actions for products for which a stock allocation scheme is active (implement and monitor allocation decisions)
Respond to the Finance Team and external provider queries
Collect and provide required documents to the auditor
Act as a member of the Local Change Control Committee (CCC)
Supervise, drive & deliver on time 2nd distribution budget cycles preparation according to the Global Supply Chain Finance guidelines for the regional market scope whilst providing best quantitative, qualitative optimal & accurate insights monitoring with relevant affiliates stakeholders & facilitating with GSC finance.
In routine, pilot & secure cost to serve adherence whilst being point of alert & proactively support any possible actionable mitigation if deviating
Secure in-market Business continuity & respective back-up orchestration implementation across in-Market operations &/or actively mitigate any risks detected that may impact (Supply Chain manual update)

Interested? For this role we’re looking for the following education, experience and skills

• More than 5 years of experience in Supply chain management (Planning, distribution or other relevant functions…), International Pharma/Healthcare Industry as an advantage, although related sectors or other fields can also be considered.

• Languages: Mandarin, English

• Good knowledge of supply chain and GDP/GMP concepts within the Pharma/ Healthcare industry is a plus

• Excellent communication (oral and written) and influencing skills

• High level of organizational skills and ability to balance multiple priorities

• Ability to work with minimal supervision and as part of a team

• Patient and customer focused approach to all activities

• Ability to solve issues in an efficient and compliant way

• Ability to collect, analyze and act on data to allow better decision making

• Project/process management skills

• Continuous improvement mind-set

• Proficient in Microsoft Windows, in particular Microsoft Office (PowerPoint, Excel and Word), digital tools

• Experience in database management and SAP SD MM PP – SAP H4Hana is a plus

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Rare & Epilepsy Solutions Lead (Seoul, Seoul, KR)

Make your mark for patients

MAJOR RESPONSIBILITIES
1) Collection of market and competitor information, keeping informed of all major developments, and communication of such information to Head of Rare & Epilepsy.
2) Ownership of Rare and Epilepsy Annual Brand Plans including development of local strategy together with tactical plans and campaigns to optimise sales
3) Input into pricing negotiations with health authorities and reimbursement listing
4) Input into strategic marketing plans for rare and epilepsy products
5) Significant interaction with NEUROLOGY sales team including product training, implementation of marketing / brand programs, and customer management
6) Build and maintain strong relationships with key customers in Epilepsy and gMG.
7) Close working relationship with internal stakeholders, including Regulatory Affairs, Market Access, Medical and Supply Chain departments.
8) Close working relationship with external agencies (Example: market research, advertising, medical education, medical communication, meetings management, packaging artwork)
9) Control of significant promotional investment budget of epilepsy and gMG products.
10) Act and be seen by others (internal and external) as the Rare & Epilepsy Brand Champion.
11) Prepare and lead launch preparation for Fintepla, Ristiggo and Zybrisq

COMPETENCIES
• Minumum 10 years pharma working experience.
• Preferably 5 Years Marketing experience as product manager in ethical Rx, involving a significant strategic brand.
• Marketing Project / Program implementation experience with hospital based customers (KOLs)
• Hand’s on and commercial approach to management of service agencies
• Ability to make product / marketing presentations confidently in English to management (including Global Marketing)
• High (advanced) level of written and spoken English to enable efficient communication with line manager and global / regional contacts
• Marketing Expertise with outstanding communication and presentation skills
• Patient Value Engagement: Translates patient insights from applicable sources into patient value-driven engagements.

• High level of market understanding so to create marketing programs which are consistent with brand strategy and fit local demands
• Flexible and resourceful, with a creative flare whilst retaining a practical and objective mindset.
• Ability to act on own initiative and to take ownership and responsibility.
• Strategic approach to problem solving.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

DT Lead CRM & Commercial Solutions Japan (Tokyo, Tokyo, JP)

Make your mark for patients

患者さんのためにあなたの力を発揮してください

JOB SUMMARY

The DT Lead CRM & Commercial Solutions Japan serves as the local owner of the Global Standard CRM Platform, ensuring its successful adoption, optimization, and value realization within the Japan organization. The role is accountable for defining and executing the Japan strategy, roadmap, and operational model for CRM and connected commercial technologies—such as Veeva CRM, CLM, Veeva Engage, OCCP, Case Follow System, and third‑party media integrations—while ensuring that global design principles, governance, and standardization are consistently applied.

This role acts as the bridge between global platform strategy and local business needs. By deeply understanding local commercial, medical, and regulatory requirements, the DT Lead ensures that the Global Standard Platform delivers maximum business impact in Japan through fit‑for‑purpose configuration, localized adoption support, and continuous value optimization.

The DT Lead will play a critical leadership role in Japan’s transition to the next‑generation CRM platform over the coming years—a large‑scale and complex transformation requiring strong program leadership, change management, global‑local alignment, and technology orchestration.

Leveraging expertise in business processes, data, and platform architecture, the role designs scalable and future‑ready solutions that accelerate productivity, compliance, and customer engagement. Working closely with Business functions and Digital Technology teams, the DT Lead enables data‑driven decision‑making and contributes to UCB Japan’s ambition to modernize customer experience and omnichannel engagement.

MAJOR ACCOUNTABILITIES

Act as Japan’s local owner of the Global Standard CRM Platform and Japan local commercial solutions, ensuring its successful deployment, localization, and business value realization while maintaining alignment with global governance, architecture, and design standards.
Lead the nationwide transition to the new CRM solution, managing a multi‑year, complex transformation involving global programs, business stakeholders, change management, data migration, and technology integration.
Partner closely with business units and cross‑functional teams to deploy CRM and commercial solutions that support Japan‑specific needs while adhering to global templates and standardized processes.
Collaborate intensively with Global DT/IT teams (Architecture, Centers of Excellence, Operations, Support) to co‑design capabilities, resolve platform gaps, ensure consistent implementation, and secure effective transition into global support models.
Manage third‑party vendors and implementation partners, coordinating development, configuration, and rollout activities, and ensuring deliverables are of high quality and aligned with platform strategy.
Provide strategic direction and prioritize solution enhancements, ensuring a balanced approach between global product roadmap, local regulatory requirements, and Japan business priorities.
Lead end‑to‑end project and program management, ensuring delivery on time, within scope and budget, and in accordance with quality and compliance expectations.
Translate business requirements into platform‑aligned architecture specifications, defining processes, integrations, and data flows that meet Japan needs while maintaining global consistency.
Create and maintain architecture artifacts that clarify end‑to‑end solution design, including integration maps, domain models, and reference architectures.
Ensure adherence to enterprise architecture and governance standards, embedding controls in PMO processes, SDLC, change management, and procurement to sustain long‑term platform integrity.

Experience & Skills

Bachelor's Degree or above
5+ years of experience in CRM, commercial and project management.
Experience in latest CRM, commercial related tools and technologies: Veeva CRM, SFMC, SFHC, GA4, M3, PowerBI, etc.
3+ years of experience in Pharmaceutical industry

COMPETENCIES

Strong passion for CRM, platform innovation, and business transformation, with a clear understanding of how global platform capabilities can improve decision‑making and patient/HCP outcomes in Japan.
Continuously monitors global and local trends in CRM, commercial technologies, omnichannel engagement, and AI, applying insights to optimize adoption and maximize local value.
Strong strategic and analytical skills to translate Japan business needs into structured objectives, clear requirements, and globally aligned solutions – Global and Japan specific solutions.
Demonstrates adaptability, creativity, and resilience in leading large‑scale transformation, particularly in multi‑year global‑local CRM migration initiatives.
Thinks holistically and long‑term, identifying high‑impact opportunities and enhancements that elevate customer engagement and system performance in Japan.
Excellent collaboration and influence skills, working effectively across DT/IT, business teams, global stakeholders, and external partners.
Fluent in Japanese and English

患者さんのために価値を創造し、ご自身の力を発揮する準備ができているとお感じでしたら、ぜひ私たちにご連絡ください。

会社概要

UCBで働く魅力

UCBでは、単に業務をこなすのではなく、価値を創造することを大切にしています。私たちは挑戦を恐れず、協力し合い、革新を追求しながら、患者さんのために成果を出すことを目指しています。
誰もが尊重され、受け入れられ、最善を尽くせる平等な機会がある、思いやりと支援に満ちた文化が根付いています。
私たちは常に「その先」を目指し、患者さん、社員、そして地球に対して人間らしさを大切にした価値を提供しています。
UCBで働くことで、自分自身の成長を実感し、自由にキャリアを築き、可能性を最大限に引き出すことができます。

UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。

選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください：

EMEA-Reasonable_Accommodation@ucb.com

※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。

Medical Solution Lead (Shanghai, Shanghai, CN)

Make your mark for patients

The Medical Advisor will report to Medical Strategy Lead (China), who is responsible for the assigned therapeutic area to provide the bridge between clinical research and commercial department as well as the remaining departments within the organization. The Medical advisor will align with global strategies to develop China local medical strategy and medical plan for assigned therapeutic area, provide medical/academic insights for marketing strategy/plan and cross-functional professional support (including but not limited with post-marketing clinical trials) medical training and academic communication, build up and maintain academic relationship with top KOLs.

You will provide the professional medical advice to healthcare organizations, ensuring compliance with regulations. Responsibilities include developing local medical strategy, programs and medical materials, reviewing medical data, advising on clinical development, and liaising between medical and non-medical staff.

Experience：

• Master of clinical medicine, bio-pharmaceutical or biotechnology as minimum.

• More than 1 year in clinical practice is preferred;

• More than 5 years in pharmaceutical company, including 2 years medical strategy role, specialized in neurology is preferred;

• Previous experience in Clinical Research and/or Drug Development is a plus.

• Firmly grounded in scientific fundamentals of experimental protocol development and methodology, data interpretation and scientific communication;

• Capable of developing Country Medical strategy and tactics;

• Business insights and marketing sense (good understanding pharmaceutical business)

• Ability to function in a team-oriented (matrix) environment

• Ability to think strategically to guide publication-related activities in accordance with industry standards and good publication practices

• Knowledge in ICH, GCP and local regulations;

• Fluent English in literature reading, medical writing and oral communication, can independently communicate with global;

• Leadership without authorization

• Excellent Project management skills and Budget control

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Stagiaire Environnement & Système HSE (Bulle, Gruyere, CH)

Make your mark for patients

Pour soutenir son département « Manufacturing Support au sein du Groupe HSE», UCB Farchim SA à Bulle en Suisse est à la recherche, pour une durée de 6 mois (avec possibilité de prolongation de 2 mois), d’un.e :

Stagiaire Environnement & Système HSE

Dans le cadre de l’évolution des activités du site, le département HSE souhaite renforcer la conformité réglementaire et améliorer la gestion environnementale en actualisant ses outils et ses processus.

Missions principales :

Veille réglementaire :

Mettre en place et adapter le nouvel outil de veille réglementaire HSE.
Identifier et intégrer les exigences légales applicables.

Documentation environnementale :

Mettre à jour et structurer les documents liés aux aspects environnementaux (plans d’action, SOP).
Assurer la traçabilité et la conformité des informations.

Analyse environnementale :

Participer à l’analyse des risques environnementaux et au suivi des plans d’action.
Collecter les données terrain en collaboration avec les équipes opérationnelles.
Communiquer et motiver des équipes non spécialisées pour une approche pragmatique et efficace.

Profil souhaité :

Étudiant·e en ingénierie, HSE, environnement ou domaine connexe.
Intérêt pour la réglementation suisse et européenne en matière de sécurité et d’environnement.
Autonomie, rigueur, esprit d’analyse.
Maîtrise des outils informatiques (Excel, Word, SharePoint).
Excellentes compétences en communication et vulgarisation.
Une expérience en industrie pharmaceutique (environnement GMP) est un plus,
Organisation et gestion de projet.
Français obligatoire et anglais en plus

Compétences clés :

Connaissance des réglementations HSE.
Capacité à travailler en équipe et à interagir avec des interlocuteurs variés.

Nous offrons un stage rémunéré dans un cadre dynamique d’une durée approximative de 6 mois (avec possibilité de 2 mois supplémentaire); date d’entrée en fonction: négociable selon les disponibilités.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Quality Control Microbiology Specialist (Bulle, Gruyere, CH)

Make your mark for patients

We are looking for an experienced, detail-oriented, and collaborative Quality Control Microbiology Specialist to join our team at our Bulle site in Switzerland.

About the role

You will maintain and develop microbiological laboratory activities in alignment with our company vision, ensuring compliance with GMP and quality standards. Your role includes supporting microbiological operations, driving continuous improvements, and fostering a strong quality culture on site.

Who you’ll work with

You will collaborate closely with internal teams including Manufacturing, Supply Chain, Technical Services, Quality Compliance, HSE, and Manufacturing Support, as well as with other UCB sites globally to ensure quality excellence.

What you’ll do

Provide SME (Subject Matter Expert) support for microbiological methods and laboratory equipment.
Lead troubleshooting, deviations, and investigations related to microbiology lab methods.
Support laboratory teams and participate in the implementation of new microbiological methods.
Establish and maintain effective relationships with internal and external stakeholders.
Contribute to SOPs, Product Quality Reviews, and continuous process verification.
Promote and implement process improvements aligned with Quality and HSE standards.

Interested? For this role we’re looking for the following education, experience and skills

Master’s degree or equivalent experience in lab technology, microbiology, or related field.
5+ years of experience in Quality Control within the biopharmaceutical industry.
Knowledge in environmental monitoring and microbiology.
Strong problem-solving, statistical, and project management skills.
Familiarity with GMP, pharmacopeia standards, and regulatory requirements.
Leadership skills with the ability to maintain team spirit and train others.
Proficiency in French and English.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Method & Support Trainee (Bulle, Gruyere, CH)

Make your mark for patients

Nous recherchons un Stagiaire en ingénierie mécanique qui est rigoureux, collaboratif et orienté amélioration continue pour rejoindre notre équipe Method & Support, basée dans notre bureau de UCB à Bulle, Suisse

À propos du rôle

UCB est une société biopharmaceutique mondiale spécialisée dans les troubles neurologiques et l’immunologie. Pour soutenir le Pôle fiabilité du site, ce stage de 6 mois vise à renforcer la fiabilisation des équipements de production. Le rôle consiste à conduire des travaux d’amélioration continue, à réaliser des AMDEC sur des équipements critiques et à structurer la base de données dédiée afin d’assurer la qualité, la cohérence et la pérennité des analyses.

Avec qui vous travaillerez

Vous collaborerez directement avec les équipes de production, les services support et nos partenaires industriels. Vous serez accompagné(e) par l’équipe fiabilité du site, qui vous guidera dans la réalisation des AMDEC, la priorisation des actions et la mise en œuvre des améliorations. L’environnement est dynamique, multidisciplinaire et orienté performance.

Ce que vous ferez

• Identifier les modes de défaillance des moyens de production

• Évaluer les effets sur qualité, sécurité et disponibilité

• Prioriser les actions pour réduire les pannes et améliorer la performance

• Structurer et maintenir la base de données dédiée aux AMDEC

• Standardiser le processus de mise à jour des AMDEC

• Participer à la mise en œuvre des améliorations fiabilité

Intéressé(e) ? Pour ce rôle, nous recherchons la formation, l’expérience et les compétences suivantes

• Cursus ingénieur/master en génie mécanique ou équivalent

• Intérêt marqué pour l’industrie pharmaceutique

• Aisance relationnelle et esprit de collaboration

• Capacité à travailler avec des équipes multidisciplinaires

• Motivation pour les démarches d’amélioration continue

• Maîtrise du français obligatoire

• Maîtrise de l’anglais appréciée

• Disponibilité pour un stage rémunéré de 6 mois dès 2025

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

External Manufacturing Operations Lead (Bulle, Gruyere, CH)

Make your mark for patients

We are looking for an External Manufacturing Operations Lead to join us in our External Manufacturing Department, based in Bulle in Switzerland.

About the role

As the External Manufacturing Operations Lead for Drug Substance, you will be responsible for the overall performance of contract manufacturing organizations (CMOs) and key suppliers within your portfolio (here in identified as third parties). Your focus will be on ensuring reliable supply, prompt issue resolution, and strong partnerships with stakeholders. You will guide the UCB vendor team (a team dedicated to management of given third party) and act as the primary contact and relationship manager with third parties, maintaining strong connections to ensure sites meet expectations and UCB needs.

Who you’ll work with

In this role, you will collaborate closely with cross-functional and matrix teams within UCB, as well as with third parties leadership teams and strategic vendors. Your daily interactions will include internal stakeholders from various UCB functions, external business partners, and senior management members of third parties. Through these partnerships, you will foster effective communication, drive operational excellence, and ensure that all parties are aligned toward achieving shared goals.

What you’ll do

Support reliability, robust processes, prompt issue resolution, and strong partnerships with vendors and internal stakeholders
Guide third parties vendor teams, coordinating cross-functional and inter-company activities
Participate in projects to foster operational excellence within UCB external manufacturing
Maintain governance structures and facilitate regular meetings between CMOs and UCB teams
Conduct operational performance evaluations and management processes for third parties
Provide operational expertise to support effective processes and optimized capacity utilization
Lead troubleshooting and investigations in collaboration with third parties, coordinating corrective actions
Identify and deliver continuous improvement projects to enhance quality, cycle times, and cost efficiency
Ensure compliance with regulatory standards and industry regulations
Prepare business and operations plans, defining operational management based on commercial strategy
Manage risks, including capacity availability and potential supply chain disruptions
Monitor third parties capacities and implement long-range product plans
Share technology knowledge, market intelligence, and product knowledge

Interested? For this role we’re looking for the following education, experience and skills

Master’s degree or PhD in life sciences with at least 7 years of relevant experience
Knowledgeable in technical and manufacturing aspects related to the portfolio area
Ability to lead multi-functional teams, motivate others, ensure responsibility, and focus on goals
Skilled in managing external business partners and relationships
Basic knowledge in financial and business knowledge. Capable of developing and analyzing business cases
Able to clarify complex technical and manufacturing performance issues
Capable of summarizing and presenting scenarios to support decision-making
Experience in crisis management and related communication
Strong problem-solving, project management and strategic thinking
Experience in operational excellence is a plus
Fluent in English (written and spoken), French is a plus

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Digital Business Analyst Trainee (Bulle, Gruyere, CH)

Make your mark for patients

Nous recherchons un Stagiaire en Ingénierie de gestion / génie industriel qui est dynamique, autonome et curieux/se pour rejoindre notre équipe service digital / amélioration continue, basé dans notre site de production de Bulle à Bulle, Suisse.

À propos du rôle

En tant que Business Analyst stagiaire chez UCB, vous jouerez un rôle central dans la compréhension et l’amélioration des processus métiers au sein d’un site biopharmaceutique. Vous interviendrez sur des projets variés où qualité et transformation digitale sont prioritaires.

Avec qui vous travaillerez

Vous collaborerez avec les équipes opérationnelles et le Digital Transformation Lead pour analyser, modéliser et améliorer les processus. L’équipe est multidisciplinaire et centrée sur la valeur apportée au client.

Ce que vous ferez

• Analyser les processus existants et identifier les pistes d’amélioration
• Recueillir les besoins auprès des utilisateurs via ateliers et interviews
• Modéliser les processus avec BPM, diagrammes et cartographies
• Contribuer à la définition de solutions digitales (automatisation, Power Platform)
• Créer des dashboards Power BI pour le suivi des performances
• Accompagner les équipes dans l’adoption des nouvelles solutions

Intéressé(e) ? Pour ce rôle, nous recherchons

• Bachelor ou Master en Ingénierie de gestion / génie industriel
• Bonne compréhension de la modélisation de processus
• Intérêt marqué pour la transformation digitale et les environnements industriels
• Capacité d'analyse, esprit critique et curiosité
• Aisance relationnelle et collaboration avec équipes multidisciplinaires
• Notions d’outils digitaux : Power BI, QlikSense, Power Apps, Excel avancé
• La connaissance du secteur biotechnologique et pharmaceutique est un atout
• Bonne compréhension de l’anglais

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Laboratory Technician (Bulle, Gruyere, CH)

Faites la différence pour les patients

Nous sommes à la recherche d’un/e Laboratory Technicien pour rejoindre notre département Quality Control, basée dans notre site de production biotechnologique, pharmaceutique et chimique à Bulle, Suisse.

Concernant le rôle

Le Technicien(ne) de Laboratoire est responsable d’effectuer les essais analytiques conformément aux instructions reçues dans les conditions préétablies de qualité (exacts et fiables), de temps, de conformité technique, d’hygiène, de sécurité et de respect de l’environnement.

Vos activités

Réalisation des analyses : Effectuer des tests selon les instructions et les pharmacopées en vigueur.
Fiabilité des résultats : Restituer des résultats justes et fiables, et vérifier les analyses des collègues.
Gestion des sous-traitances : Envoyer des analyses à sous-traiter et traiter les résultats reçus.
Amélioration continue : Proposer des mesures pour améliorer la précision et réduire les coûts.
Rédaction des procédures : Participer à la rédaction et à la mise à jour des procédures.
Entretien du matériel : Respecter et entretenir le matériel et les locaux.

Intéressé/e ? Pour ce poste, vous devez posséder la formation, l'expérience et les compétences suivantes :

CFC de laborantin(e) en chimie ou diplôme équivalent.
Expérience en chimie analytique et instrumentale exigée.
2+ ans expériences dans un laboratoire qualité (GMP).
Expérience dans l’industrie pharmaceutique sera un plus.
Techniques d’analyses, dépendant des analyses attribuées (H-UPLC, GC, KF, UV, IR, Potentio, etc).
Connaissance de Pharmacopée (européenne, américaine, japonaise).
Informatique : maîtrise d’Office (Excel, Word, Access), maîtrise d’Empower et/ou d’un LIMS un plus.
Être autonome dans son travail, sens de l’organisation, esprit d’initiative.
Curiosité et esprit critique.
Capacité à apprendre de nouvelles techniques.
Bonne communication.
Esprit d’équipe.
Langues : Français (écrit et à l’oral).

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

UCB est une société biopharmaceutique mondiale, spécialisée dans la neurologie et l'immunologie. Nous sommes plus que 9.000 personnes aux quatre coins du monde, inspirées par les patients et motivées par la science.  

Pourquoi travailler pour nous ?

Chez UCB, nous ne nous limitons pas à réaliser des tâches, nous créons de la valeur. Nous ne craignons pas d'aller de l'avant, de collaborer et d'innover pour faire la différence auprès des patients. Nous avons une culture de bienveillance et solidarité où chacun se sent inclus, respecté et a des chances égales de faire de son mieux. Nous allons au-delà pour créer de la valeur pour nos patients, et toujours dans une optique humaine, que ce soit pour nos patients, nos employés ou notre planète. En travaillant pour nous, vous découvrirez un monde où vous pourrez grandir et aurez la liberté de tracer votre propre parcours professionnel et accomplir votre plein potentiel.

Chez UCB, nous avons adopté une approche hybride du travail, réunissant les équipes dans des hubs locaux pour favoriser la curiosité collaborative. Sauf mention contraire dans la description du poste ou incompatibilité avec ses missions, ce poste est hybride, avec 40 % du temps de travail effectué au bureau.

UCB est un employeur qui promeut l'égalité des chances. Toutes les décisions d'embauche seront prises sans tenir compte de toute caractéristique protégée par les lois applicables. Si vous avez besoin d'ajustements à notre processus de recrutement afin de mettre en valeur vos compétences, veuillez nous contacter à l'adresse EMEA-Reasonable_Accommodation@ucb.com. À noter que si votre message ne concerne pas une demande d'ajustements, nous ne pourrons pas vous assister par ce biais.

Technicien·ne de Production Pharmaceutique (Bulle, Gruyere, CH)

Make your mark for patients

Nous recherchons un·e Technicien·ne de Production Pharmaceutique, autonome, rigoureux·se et flexible, pour rejoindre notre équipe Pharma DP, basée sur notre site à Bulle, Suisse.

Le poste est organisé en horaires d’équipe 3x8.

À propos du poste

Le rôle consiste à conduire en autonomie plusieurs opérations de production pharmaceutique dans le respect des normes cGMP, des règles HSE, des exigences de qualité et des objectifs de coûts et délais. Il implique la manipulation d’équipements industriels, la réalisation d’opérations techniques variées, la documentation des activités et la participation active à l’amélioration continue.

Avec qui vous travaillerez

Vous travaillerez au sein de l’équipe Pharma DP, en collaboration avec des techniciens expérimentés, des responsables de production, les équipes Qualité, Maintenance et HSE. L’environnement est structuré, exigeant et orienté vers la sécurité, la conformité réglementaire et la performance opérationnelle.

Ce que vous ferez

Réaliser pesée, mélange, broyage, tamisage et opérations associées.
Conduire compression, pelliculage, inspection visuelle et tests IPC.
Effectuer transferts de solides/solutions et opérations d’essorage.
Nettoyer et désinfecter équipements et zones de production.
Compléter documents de production et systèmes électroniques (PRC, SAP, XFP).
Ajuster paramètres, réagir aux anomalies et prévenir dysfonctionnements.
Participer validations, qualifications et actions d’amélioration continue.
Respecter cGMP, procédures, règles HSE et exigences du site.

Profil recherché : formation, expérience et compétences

Certificat Fédéral de Capacité (CFC) ou formation technique équivalente.
Connaissance équipements industriels et produits chimiques utilisés.
Compréhension d’un système qualité GMP ou ISO.
Capacité à travailler en zones contrôlées et appliquer règles HSE.
Autonomie, rigueur, sens de l’observation, communication aisée.
Maîtrise du français oral et écrit.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Biotech Manufacturing Technician USP (Bulle, Gruyere, CH)

Make your mark for patients

Nous sommes à la recherche d’un/e Biotech Manufacturing Technician USP qui soit motivé(e) pour rejoindre notre équipe de production, basée sur notre site de production biotechnologique, pharmaceutique et chimique à Bulle, Suisse.

Concernant le rôle

En tant que Biotech Manufacturing Technician USP vous assurez les activités de la production biotechnologique upstream en shift 5x8, avec les délais et la qualité requise nécessaire au bon fonctionnement des opérations.

Vous aimez travailler dans un environnement où vous pouvez :

Faire partie d’une équipe très collaborative et soudée.
Participer à la production des médicaments qui vont améliorer la qualité de vie des patients.
Travailler pour une des rares entreprises à travers le monde qui réunissent des plateformes à la fois biotechnologiques et chimiques sur un seul et même site de production.

Vos activités :

Assurer la production de notre produit biologique en fonction du planning établi et avec la qualité requise pour maintenir la continuité des opérations.
Assurer que la zone USP ainsi que les opérations effectuées dans celle-ci soient en accord avec les règles GMP.
Effectuer des tests IPC.
Renseigner et/ou vérifier les documents de production
Participer à la mise en place des concepts nécessaires pour les activités de production et assurer leur application.
Participer à la création et la modification de la documentation de production : procédures, recettes.
Maintenir la zone et ses équipements dans un état propre (nettoyage).
Intervenir et résoudre les problèmes de premier niveau de la zone de production et les remonter au responsable de zone.
Respecter les règles HSE et particulièrement : respect des procédures, port des équipements de protection individuelle, utilisation systématique des éléments de sécurité, tri et identification des déchets, signalisation des fuites.
Assurer une bonne intégration des nouveaux collègues et les aider dans leur formation.
Assurer une traçabilité rigoureuse de la formation.
Participer à l’amélioration continue de la zone de production.

Ponctuellement :

Participer aux lots de validation pour le lancement de nouveaux produits
Participer aux activités de tests lors des qualifications des équipements process.

Intéressé/e ? Pour ce poste, vous devez posséder la formation, l'expérience et les compétences suivantes :

Formation technique / HES Biotechnologie / CFC laborantin/e en chimie/biologie, ou expérience équivalente.
Connaissance des BPF et des exigences liées à l’environnement pharmaceutique.
Expérience et à l’aise avec les systèmes d’automation (niveau utilisateur).
Flexibilité (travail en horaire décalé/weekend/nuit 5x8).
Suivi des procédures et des méthodes de production. Capable de fournir un travail soigné et de qualité.
Très bon sens de la communication.
Fort esprit d’équipe.
Esprit logique et pratique.
Bonne maîtrise du français (oral et écrit) ; l’anglais est un atout.
Expérience dans l’industrie biotechnologique, chimique ou pharmaceutique est un plus.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global SME Clean et Black Utilities (Bulle, Gruyere, CH)

Make your mark for patients

We are looking for a Global Clean & Black Utilities Expert, who is eager to join our Engineering & Sites and Facilities department, based in our manufacturing site in Bulle, Switzerland.

About the role

UCB is transforming the way we manage physical assets across all sites worldwide. As part of this transformation, we are looking for a Global Clean & Black Utilities Expert to join our Physical Asset Management organization within Engineering & Sites & Facilities (ESF).

In this global expert role, you will shape UCB’s strategy for clean utilities and selected non-GMP utility and waste systems, ensuring consistency, innovation, compliance, and safety across all CAPEX and lifecycle projects.

You will be the reference for Clean Utilities globally and play a critical role in defining standards, driving innovation, and influencing major engineering programs across Belgium, Switzerland, the US, Japan, and the UK.

Who you’ll work with

The Physical Asset Management / Asset Technical Standards & Expertise Team.
Engineering & Sites & Facilities project leads.
Global network of experts and external partners (e.g., ISPE).
Asset owners, users, and design engineering leads.
EHS, Quality, and manufacturing stakeholders worldwide.

Your expertise will directly contribute to UCB’s global technical excellence and long-term asset strategy.

What you’ll do

Define and develop global technical standards for clean utilities, gas systems, water pretreatment, and waste systems, integrating safety, sustainability, and regulatory requirements.
Lead the global strategy for utility-related systems on all engineering CAPEX projects and contribute expertise during design reviews and technical assessments.
Provide expert guidance to engineering teams, asset owners, and project leads to ensure robust technical solutions aligned with cGxP, EHS, and Good Engineering Practices.
Monitor technological trends and drive innovation in equipment lifecycle management, digitalization, and sustainable engineering solutions.
Build and lead a global network of internal and external experts, fostering knowledge flow and best-practice sharing across UCB.
Support transformation initiatives across UCB sites worldwide and contribute to technical peer reviews, gap assessments, and competency matrix development.
Act as SME for one Safety / Potential Life-Changing Activity topic (e.g., pressurized equipment, chemical storage & handling, LOTO).
Ensure technical oversight and follow-up of projects managed by Engineering & Sites & Facilities.

Interested? For this role we’re looking for the following education, experience and skills

Bachelor’s or master’s degree in engineering, Chemistry, Pharmaceutical Sciences, or a related technical field.
10+ years of experience in utilities, engineering, or technical operations in the pharmaceutical or regulated industry.
Strong technical background in clean utilities, gas systems, and waste systems in cGxP environments.
Deep expertise in clean utilities (WFI, RO, purified water, clean steam, gases) and waste systems (chemical, process, biowaste).
Strong knowledge of engineering standards, cGMP/GLP, ICH, FDA CMC, ISPE/PDA guidance.
Experience with qualification & validation (V-cycle, ASTM E2500).
Ability to interpret and set up P&IDs and Process Flow Diagrams.
Strong communication skills and ability to influence across multiple levels and functions.
Proven leadership and experience working in large, complex, international projects.
Full professional proficiency in English and French.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Laboratory Technician (shift 5X8) (Bulle, Gruyere, CH)

Faites la différence pour les patients

Nous recherchons un·e Technicien·ne de Laboratoire rigoureux·se, autonome et collaboratif·ve pour rejoindre notre équipe Quality Operations, basée dans nos bureaux de UCB à Bulle, Suisse.

À noter : poste en horaire 5x8.

À propos du poste

En tant que Technicien·ne de Laboratoire, vous réaliserez des analyses conformément aux procédures établies, dans le respect des normes de qualité, de sécurité et d’environnement. Vous contribuerez activement à la mise en œuvre de la politique HSE du site de Bulle, tout en garantissant des résultats fiables dans un environnement réglementé par les BPF.

Avec qui vous travaillerez

Vous intégrerez l’équipe Quality Operations de UCB Farchim SA à Bulle. Vous collaborerez avec des technicien·nes, des superviseur·es et d’autres départements pour assurer le bon fonctionnement du laboratoire et le respect des exigences internes et externes.

Ce que vous ferez

Réaliser des analyses selon les pharmacopées EP, USP, JP et les procédures internes.
Garantir des résultats justes, fiables et documentés.
Effectuer des double-checks et des analyses hors-routine.
Gérer les échantillons sous-traités et traiter les résultats reçus.
Participer aux projets internes et aux validations d’équipements et logiciels.
Respecter les règles HSE et contribuer à l’amélioration continue du laboratoire.
Travailler principalement sur analyses HPLC et U(H)PLC, conformément à votre expérience.

Intéressé·e ? Voici les formations, expériences et compétences requises

CFC de laborantin·e en chimie/biologie ou équivalent reconnu.
3+ ans d’expérience en laboratoire qualité sous BPF.
Maîtrise des techniques : HPLC/U(H)PLC, UV et électrophorèse capillaire est un atout. ELISA est un plus.
Connaissance des pharmacopées et des exigences GMP.
Bon niveau en français, lecture de l’anglais technique.
Maîtrise d’Office ; Empower ou LIMS est un atout.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

MES Engineer (Bulle, Gruyere, CH)

Make your mark for patients

We are looking for a MES Engineer who is meticulous, a team player, and proactive to join our Technical Services department, based at our biotechnology, pharmaceutical, and chemical production site in Bulle, Switzerland.

About the Role

The mission of the MES Engineer is to perform programming, testing, and documentation activities, participate in projects as a Subject-Matter Expert in Automation, and handle maintenance of automated and computerized production systems.

Work environment

Report to the Automation Manager and work in a team of 10 people, within the Automation team consisting of 18 members.
Be part of a dynamic and collaborative team, with a positive and solutions-oriented mindset allowing for knowledge sharing.
Participate in improving the quality of life of our patients.

Your Activities

Carry out programming activities, system maintenance, FAT/SAT, and commissioning.
Handle DITs (technical intervention requests) by applying best practices in analysis, programming, and verification.
Contribute as an automation expert to the execution of technical projects.
Manage and prioritize routine activities while ensuring continuity of production operations.
Coordinate and support the technical activities of external resources involved in DITs and projects.
Ensure the document life cycle (writing, verification, approval, regular update) for all project or routine activities.
Handle deviations, investigations and CAPA (corrective actions and preventive actions) at the technical and documentation level.
Actively participate in the production support plan (“On Call”) according to the annual plan, ensuring ongoing availability (24/7/365) of automation expertise.

Interested? For this position, you must possess the following education, experience, and skills:

Bachelor’s degree or higher in Automation/Computer Science or equivalent.
Over 5 years’ experience in Syncade (DeltaV MES) programming.
Pharmaceutical or biotech industry experience preferred.
Familiarity with administrating MES or DCS systems would be an advantage.
Effective communication and leadership skills.
Fluent in French and English.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head Qualification, Validation, Digital and Data Integrity (Switzerland) (Bulle, Gruyere, CH)

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To strengthen our Global QA Compliance Operations department, part of Internal Manufacturing Quality (IMQ) we are looking for a talented profile to fill the position of: Head Qualification, Validation, Digital and Data Integrity – Switzerland, Bulle

About the role

The Head of Head Qualification, Validation, Digital and Data Integrity, is a senior position within the Quality Compliance Operations team, reporting directly to the Head of QA Compliance Operations.

The position focus will be to ensure strategic oversight, harmonization, and continuous improvement of Qualification and Validation activities across all internal manufacturing sites; the coordination of Data Integrity Roadmap execution and monitoring; and align with processes being followed also by the External Manufacturing organization.

This strategic role ensures that Qualification, Validation, Digital, and Data Integrity systems across all UCB operational sites are designed, implemented, and maintained in a harmonized and consistent manner in alignment with the evolving regulatory requirements and internal company standards

While executing these Global activities the role needs to foster a culture of continuous improvement, process optimalization, driving operational excellence and implement process and value driven Digitalization, and collaborate with key stakeholders globally across UCB Units to uphold and enhance the organization’s quality standards.

You will work with

In this role, you will work closely with various stakeholders across UCB's internal and external manufacturing organizations. You will collaborate with the Internal Manufacturing Quality Assurance Leadership team, the QA Compliance Operations Leadership team ensuring alignment and harmonization of Qualification, Validation, Digital and DI activities, across all operational sites. Additionally, you will engage with the External Manufacturing organization to align processes. You will also interact with key stakeholders globally across UCB Units to foster a culture of continuous improvement, process optimization and wherever there is a process and value driven digitalization opportunity while supporting the organization’s quality standards.

What you will do

Lead a global quality team who supports operational and strategic activities, provide development opportunities while being value driven.
Conduct Gemba sessions across UCB Sites/ Departments to understand existing quality processes part of the role and systems, identify inefficiencies and identify Value Digitalization when needed.
Oversee Computerized Systems Validation (CSV) and champion DI initiatives, ensuring compliance with global DI standards and best practices of industry.
Oversee automation projects to optimize manufacturing quality executions.
Ensure quality oversight across IM, including deviations related to qualification, validation, and testing executed.
Coordinate the Data Integrity Roadmap execution, covering both paper documentation and systems.

Drive harmonization and standardization of quality practices related to Qualification/ Validation, DI execution (DIRA, audit trail…) across IM sites, fostering consistency and compliance globally.

Support quality improvement programs or/and initiatives aiming at enhancing efficiency, reducing risks, and maintaining high standards of compliance.
Support audit and inspection readiness when required, ensuring sites are prepared for internal and external reviews.
Promote a culture of innovation and continuous learning within the team and across the organization.

Oversee the training matrix, onboarding and development of people within the team.

Serve as the transversal IMQ Single Point Of Contact (SPOC) for Quality Compliance topics below:

CSV, Testing and Access management
Data Integrity (DIRA, audit trail...)
Cleaning Validation, disinfectant Validation
Qualification management (IQ, OQ, PQ)
Utilities, facilities
Maintenance & Metrology

Partner with key stakeholders to ensure alignment on quality processes and build regular networking communication (e.g. monthly meeting, monthly gemba...).
Integrate any new IM UCB site into the Qualification, Validation, Digital, and Data Integrity framework by defining and executing a comprehensive strategy.

Interested? For this position you’ll need the following education, experience and skills

Bachelor’s, master’s degree or an education in a relevant scientific discipline
Minimum of 10 years in Quality Assurance or/and Quality Systems Operations or/and Quality Compliance within a regulated pharmaceutical environment or equivalent
Fluent English communication (oral and written); any additional languages are a plus
Deep understanding of cGMP principles and global regulatory environments
Proven track record in leading a team of people across the world
Experience in participating in audits and inspections (FDA)
Experience in Value driven Digitalization is a plus
PMO, green belt, lean & six sigma is a plus
Excellent organizational and analytical abilities to manage projects
Expertise in data integrity, computerized systems validation, and process automation.
Expertise with quality processes: maintenance & metrology, utilities, facilities, qualification (IQ, OQ, PQ), cleaning validation, disinfectant validation
Exceptional communication and interpersonal skills for effective stakeholder engagement
Strategic & Critical thinking with the ability to foster a culture of Quality, Continuous Improvement and Innovation

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Immunology Lead Scandinavia (Stockholm, Stockholm, SE)

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Do you have the vision and drive to shape the future of immunology care in the Scandinavian countries? We’re looking for an empowering and forward‑thinking Immunology Lead Scandinavia, to elevate patient value, ignite cross‑functional collaboration, and steer the Immunology franchise across Rheumatology and Dermatology. This is your opportunity to make a meaningful impact—both for patients and the healthcare ecosystem.

About the role

In this commercial leadership role, you will orchestrate all activities of the Local Patient Value (LPV) unit and lead the franchise at the Scandinavian level. You will translate deep therapeutic expertise and ecosystem knowledge into powerful strategies that advance UCB’s immunology objectives and elevate patient value across Scandinavia. You will ensure that local strategies reflect global and Nordic priorities while fostering strong partnerships with healthcare stakeholders, patient organizations, and internal ecosystem teams.

Who you’ll work with

You will collaborate with internal local patient value unit colleagues, scientific leads, area heads, and external stakeholders such as KOLs, clinics, payers, and patient advocacy groups.

What will you do

Demonstrate motivational, inclusive cross-functional leadership built on UCB’s Patient Value Strategy.
Shape strategy and drive execution of patient value plans.
Build partnerships across the Scandinavian healthcare ecosystem.
Deliver performance, forecasting, and compliance excellence.
Be an active contributor in Immunology Nordic Leadership Team
Develop and manage key processes to gather insights to pro-actively manage the complexity of and relevant value drivers in the ecosystem

Interested? For this position you’ll need the following education, experience, and skills:

Extensive commercial experience in the pharmaceutical industry.
A visionary and ambitious leader with strong strategic muscle, and several years in a leadership role in the Immunology (Dermatology & Rheumatology) area with proven ability to lead cross-functional and matrix teams
Ability to develop and coach individuals and team to joint accountability and high performance
Languages: Swedish or Danish & English
Deep understanding of the Scandinavian healthcare ecosystem and key value drivers
Strong strategic planning, business acumen and analytical skills
Demonstrated excellence in stakeholder engagement and collaboration
Strong communication skills and customer focus

Deadline for applications: 13th of March

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Key Account Manager (Field Based, Field Based, CH)

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We are looking for a Key Account Manager Immunology to join us in our local commercial operations team, field-based in Eastern Switzerland.

About The Role

As Key Account Manager Immunology you inform office- and hospital-based dermatologists with positivity and engagement about the benefits of our innovative and newly launched product and establish impactful projects for our solutions and therapy approaches.

You like to work in an environment where you can

Be part of a very collaborative team who works towards a common goal: improving patient’s life's.
Be responsible for the assigned target groups of dermatologists in the territory (office- and hospital-based HCPs and relevant account stakeholders).
Proactively initiate, organize, and implement educational events in cooperation with the Medical Science Liaison (MSL) and internal stakeholders.

What You’ll Do

Building and strengthening mutually beneficial and sustainable customer relationships and ensure that the strategic and tactical objectives within your territory are met.
Cross functional collaboration & account planning: Work closely with internal teams to develop & align field force strategies and activities to ensure seamless service delivery.
Ensuring the implementation of defined activities in accordance with strategic account plans.
Using multiple communication channels (face to face & digital) to contact health care specialists.
Establishing UCB as valued partner in the immunology area in close collaboration with Medical Science Liaison (MSL).
Overseeing the periodical reporting for the First Line Manager and documentation in the CRM system.

Interested? For this role we’re looking for the following education, experience and skills

You have passed a medical, paramedical, pharmaceutical, or scientific education.
You have a minimum of 3 years of sales experience within the pharmaceutical industry, ideally in immunology.
Experience and relationships in dermatology will be a plus.
You have a proven expertise in strategic account planning.
You are a team player and appreciate working in cross-functional teams.
Fluent in German and good knowledge in English.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Lead Immunology ECE (Field Based, Field Based, PL)

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We are looking for a Medical Lead Immunology ECE (East Central Europe Cluster),who is eager to join our department, based in our office in Warsaw, Poland.

About the role

As Medical Lead Immunology ECE (East Central Europe), you will provide strategic, scientific, and people leadership for the Immunology medical organization in the East Central Europe Cluster (Poland, Czech Republic, Slovakia, Hungary).

You will be accountable for setting and executing the medical strategy across the region, ensuring alignment with global and regional priorities, and for leading, developing, and inspiring a team of Medical Science Liaisons (MSLs) and Medical Solution Leads.

You will act as a senior medical leader and scientific expert, shaping the value story of UCB’s immunology portfolio and ensuring high-quality scientific exchange with both internal and external stakeholders, always in line with the highest ethical and compliance standards.

Who you’ll work with

You will work in close partnership with:

The Head of Medical, East Central Europe Cluster, to align on strategy, capabilities, and talent development
Regional and global Immunology and Medical Affairs teams
Cross‑functional stakeholders including commercial, market access, evidence generation, and ecosystem leadership teams
External stakeholders such as key opinion leaders, advocacy partners, and decision-makers across the region

The Immunology MSLs and Medical Solution Leads in the ECE Cluster report directly to this role.

What you’ll do

Lead and develop the Immunology medical team

Lead, coach, and develop a regional team of MSLs and Medical Solution Leads
Recruit, onboard, and retain top medical talent across the ECE Cluster
Drive a strong culture of scientific excellence, collaboration, accountability, and compliance
Define objectives, KPIs, and development plans in alignment with cluster and global priorities

Shape and execute medical strategy

Develop and implement regional immunology medical strategies and roadmaps aligned with global and EU direction
Provide medical input into local Integrated Strategy Plans (ISPs) and ecosystem plans
Ensure high-quality planning, execution, and performance tracking of medical activities in the field

Act as a scientific and strategic partner

Serve as a subject matter expert in immunology, ensuring strong therapeutic area acumen across the organization
Translate complex scientific and clinical data into meaningful insights and value propositions
Support real‑world evidence and evidence generation activities in collaboration with regional partners

Drive cross‑functional collaboration and external engagement

Work closely with commercial, access, and medical colleagues to deliver coordinated, compliant ecosystem strategies
Engage with external experts and partners through conferences, field visits, and scientific exchange
Promote best-practice sharing and contribute to regional and global medical capability development

All activities are conducted in accordance with regulatory, legal, and compliance standards and UCB values.

Interested? For this role we’re looking for the following education, experience and skills

Advanced scientific degree preferred: MD, PharmD, or PhD.
Bachelor’s or master’s degree in a scientific discipline required.
2+ years of experience in Medical Affairs with demonstrated leadership responsibility.
Solid experience in Immunology or a closely related therapeutic area.
Proven track record in medical strategy development and execution.
Strong understanding of clinical development, study management, and real‑world evidence.
Experience working in cross‑functional, regional, or matrix environments.
Willingness to travel regularly within the region.
Strategic thinking and business acumen.
Strong scientific credibility and analytical skills.
Inspirational leadership and people development capability.
Excellent communication, storytelling, and stakeholder engagement skills.
High collaboration skills with the ability to influence without authority.
Digital literacy and comfort working in evolving medical ecosystems.
Fluency in English and Polish; additional regional languages are an advantage.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Non-Clinical Safety Lead - Cambridge, MA (Cambridge, Massachusetts, US)

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About the role

Lead, communicate, and execute non-clinical safety strategies aligned with clinical development goals.
Develop integrated non-clinical safety plans supporting innovative programs. Ensure timely delivery of high-quality non-clinical data and global regulatory documentation.
Represent UCB in interactions with regulatory authorities and external partners.

What you'll do

Provide non-clinical safety expertise to discovery and development projects
Define, lead, and implement non-clinical safety strategies across programs.
Partner with clinical teams to ensure robust preclinical data supports clinical trial design.
Contribute to global regulatory submissions (e.g., IBs, Briefing Books, INDs, NDA/BLAs) and interact with regulatory authorities.
Oversee the design, review, and interpretation of non-clinical studies.
Manage non-clinical safety programs, including budgets.

Interested? For this role you’ll need the following education, experience and skills

PhD in Toxicology, Pharmacology, or related discipline (or equivalent MS/DVM with experience).
5+ years in non-clinical safety (preferably in pharma or biotech).
Deep understanding of regulatory processes and regulatory toxicology.
Experience managing and forecasting non-clinical safety budgets.
Ability to produce high-quality reports and submission documents with subject matter expert support.

Preferred Qualifications:

Accredited or registered toxicologist.
Experience in gene and cell therapy and/or other novel modalities.

Salary:

This position’s reasonably anticipated base salary range is $168,000 to $220,500 per year. The actual salary offered will consider internal equity and may also vary depending on the candidate’s region, job-related knowledge, skills and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Content Clearance Lead (Atlanta, Georgia, US)

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We are looking for a Content Clearance Lead who is intellectually curious, self-driven, and adaptable to join our the Omnichannel and Content Operations team based in our Atlanta, Georgia office in the United States. This hybrid position requires a minimum of 40% on site presence and up to 10% domestic/international travel.

About the role
You will serve as the US business partner for the content clearance process (Review Committee or Medical-Legal-Regulatory Review) consisting of promotional and non-promotional materials. The Lead manages the review, discussion and approval of content, materials, and initiatives, with application and interpretation of regulations and industry guidance.

Who you’ll work with
You will work with Regulatory, Legal, Compliance, Medical Leads, Marketing Leads, Market Access, Patient Value Units, as well as all cross functional Subject Matter Experts and stakeholders that have input into the strategy and creation of promotional and non-promotional material.

What you’ll do

Perform initial quality reviews of materials and route submissions per internal governance standards.
Act as a Chair for Clearance Committees and lead efficient, effective content review meetings.
Partner with stakeholders to define project timelines, manage priorities, and advise on content processes.
Forecast review demand and manage approvals across planning, review, health authority submissions, dissemination and withdrawal lifecycle stages.
Ensure compliance with UCB standards and U.S. promotional labeling regulations.
Drive continuous improvement through retrospectives, deviation tracking, and root cause analysis.

Interested? For this role we’re looking for the following education, experience and skills
Minimum Education, Qualifications, Skills

Bachelor’s degree
5+ years of experience in pharmaceutical industry or life sciences industry, preferably in controlled process environment including development and approval of regulated information and materials.
Intermediate to advanced knowledge of US regulations for the promotion of pharmaceutical and biological products with proficiency in identifying emerging issues and making recommendations for resolution.
Ability to support multiple products or indications in all lifecycle stages; interpret and apply strategic business objectives to the clearance and ad/promo domain.
Excellent organization, time management, planning, and prioritization skills, with attention to detail.
Proven ability to work collaboratively and with sensitivity in a matrix organization.
Demonstrated aptitude for producing clear, concise verbal and written communications

The reasonably anticipated salary range for this position is $108,000-$141,800 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Account Executive / Scranton, PA (Scranton, Pennsylvania, US)

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To strengthen and support our launches within US Rare Disease Organization (RDO), we are seeking an Account Executive - Neuromuscular (AE) for the Scranton, PA territory that includes Hersey & Lancaster area. . The AE is an expert on the practices, delivery networks, and patient populations within their territory.

About the Role

They will represent UCB in the communities we serve as we strive to transform the lives of those living with Rare Diseases. The AE plays an integral role in identifying and building collaborative relationships with physicians and clinics. They embrace and execute marketing and sales strategies. They will master brand messaging, targeting, and digital technology to deliver persuasive, high-impact customer experiences tailored to distinct user segments while maintaining the highest ethical standards.

Who you’ll work with

Call plan physicians/HCPs and all care team members
Sales management/leadership
Market Access, Thought Leader Liaison, and Medical Teams
KOLs
Sites of care

What you’ll do

Consistently exceed territory sales objectives while operating with the highest level of ethics and integrity
Create and execute strategic business plans reflecting a thorough understanding of the local market conditions
Master targeted disease states, which include a deep understanding of patient journeys, standards of care, and treatment drivers
Advocate for Rare Disease patients and serve as the authority on the various tools and resources UCB offers to support physicians, pharmacists, and other health care providers
Continuously expand the expertise of all treating and referring physicians, as well as payers, hospital systems, pharmacies, labs, and other components of the care continuum; maintain awareness and remain attentive to the dynamics between different stakeholders that influence patient treatment decisions
Maintain strong relationships within the payer landscape to ensure providers are informed on coverage and reimbursement status; collaborate with the payer access team to ensure all relevant stakeholders are working with the most up-to-date information to maximize access and affordability for patients using UCB products
Foster strong relationships with patient advocacy groups and partners to support appropriate patient education and disease state awareness activities in the community
Collaborate cross-functionally with UCB colleagues to share insights on customer needs and market opportunities; work together towards more effective approaches to patient value creation
Maintain a commitment to continuous improvement (embrace a growth mindset) as evidenced by insights gained/shared about geography, stakeholders, and customer needs through day-to-day experience; growth in core competencies with feedback sought from managers and colleagues, courses taken, on-the-job projects and relevant periodicals/readings

Our 4 Pillars in Rare Disease Organization

Demonstrate great commitment to the Rare Disease patient community and understand the patient journey, the barriers they face in care and treatment, and how to help them overcome those barriers

Utilize innovative methods to identify patients who need treatment
Maintain a highly tactical approach to patient access
Help patients and caregivers navigate the Healthcare System and work around roadblocks

Interested? For this position, you’ll need the following education, experience, and skills:

Minimum Qualifcations:

Bachelor’s Degree
8+ years of field-based experience in sales, account management, and/or field reimbursement in biopharmaceuticals or healthcare, inclusive of 5+ years in a competitive specialty market segment
Field experience with Buy-and-Bill medical benefits, Specialty Pharmacy, and HUB delivery models
Verifiable record of sustained high sales performance and achievement in top 30% nationally
Experience/involvement in successful product launches
The ability to maximize impact of multichannel/digital tools and strategy/tactics with territory HCPs
Command of key medical, scientific, and healthcare concepts, language, and practices related to neurology and rare diseases
Experience serving a variety of call points – academic centers, community-based care, hospitals, and private office practices
Comfortable spending up to 60% of time traveling with overnight travel required (territory business need dependent)

Preferred experience

2+ years in rare/orphan drug experience in a competitive market
Significant CNS/neuroscience sales experience (to include epilepsy); Oncology, Hematology and/or Specialty reimbursement products requiring Specialty Pharmacy knowledge and expertise
Experience in supporting biologic therapy administered by a designated health care provider
Promotional product experience with REMS requirements

This positions reasonably anticipated base salary range is $137,600 - $180,600 annually. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Account Executive / Scranton, PA Sr/ (Scranton, Pennsylvania, US)

Make your mark for patients

To strengthen and support our launches within US Rare Disease Organization (RDO), we are seeking an Account Executive Sr. - Neuromuscular (AE) for the Scranton, PA territory. The AE is an expert on the practices, delivery networks, and patient populations within their territory.

About the Role

Who you’ll work with

Call plan physicians/HCPs and all care team members
Sales management/leadership
Market Access, Thought Leader Liaison, and Medical Teams
KOLs
Sites of care

What you’ll do

Consistently exceed territory sales objectives while operating with the highest level of ethics and integrity
Create and execute strategic business plans reflecting a thorough understanding of the local market conditions
Master targeted disease states, which include a deep understanding of patient journeys, standards of care, and treatment drivers
Advocate for Rare Disease patients and serve as the authority on the various tools and resources UCB offers to support physicians, pharmacists, and other health care providers
Continuously expand the expertise of all treating and referring physicians, as well as payers, hospital systems, pharmacies, labs, and other components of the care continuum; maintain awareness and remain attentive to the dynamics between different stakeholders that influence patient treatment decisions
Maintain strong relationships within the payer landscape to ensure providers are informed on coverage and reimbursement status; collaborate with the payer access team to ensure all relevant stakeholders are working with the most up-to-date information to maximize access and affordability for patients using UCB products
Foster strong relationships with patient advocacy groups and partners to support appropriate patient education and disease state awareness activities in the community
Collaborate cross-functionally with UCB colleagues to share insights on customer needs and market opportunities; work together towards more effective approaches to patient value creation
Maintain a commitment to continuous improvement (embrace a growth mindset) as evidenced by insights gained/shared about geography, stakeholders, and customer needs through day-to-day experience; growth in core competencies with feedback sought from managers and colleagues, courses taken, on-the-job projects and relevant periodicals/readings

Our 4 Pillars in Rare Disease Organization

Demonstrate great commitment to the Rare Disease patient community and understand the patient journey, the barriers they face in care and treatment, and how to help them overcome those barrier
Utilize innovative methods to identify patients who need treatment
Maintain a highly tactical approach to patient access
Help patients and caregivers navigate the Healthcare System and work around roadblocks

Interested? For this position, you’ll need the following education, experience, and skills:

Minimum Qualifcations:

Bachelor’s Degree
8+ years of field-based experience in sales, account management, and/or field reimbursement in biopharmaceuticals or healthcare, inclusive of 5+ years in a competitive specialty market segment
4+ years of Rare Disease experience in pharmaceuticals/Biologics Field experience with Buy-and-Bill medical benefits, Specialty Pharmacy, and HUB delivery models
Verifiable record of sustained high sales performance and achievement in top 30% nationally
Experience/involvement in successful product launches
The ability to maximize impact of multichannel/digital tools and strategy/tactics with territory HCPs
Command of key medical, scientific, and healthcare concepts, language, and practices related to neurology and rare diseases
Experience serving a variety of call points – academic centers, community-based care, hospitals, and private office practices
Comfortable spending up to 60% of time traveling with overnight travel required (territory business need dependent)

Preferred experience

Significant CNS/neuroscience sales experience (to include epilepsy); Oncology, Hematology and/or Specialty reimbursement products requiring Specialty Pharmacy knowledge and expertise
Experience in supporting biologic therapy administered by a designated health care provider
Promotional product experience with REMS requirements

This positions reasonably anticipated base salary range is $160,000 - $210,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Project Support Assistant (Atlanta, Georgia, US)

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We are looking for a Project Support Assistant who is organized, proactive, and detail‑oriented to join us in our Manufacturing team, based in our UCB office in the Atlanta, GA office. This hybrid position requires 40% onsite presence and 30% domestic travel.

About the role

You will play a key role in supporting large‑scale capital and regulated projects by providing high‑level administrative and coordination support. You will help project leaders and cross‑functional teams operate efficiently by managing schedules, communications, documentation, and reporting. This role requires strong organizational skills, discretion, and the ability to manage multiple priorities in a fast‑paced project environment.

Who you’ll work with

You will be working in a team that collaborates closely with project managers, executive leadership, and cross‑functional partners. You will also interact with vendors and external stakeholders, acting as a central coordination point to ensure smooth communication and alignment across project teams.

What you’ll do

Provide comprehensive administrative support for large‑scale project teams
Manage complex calendars, schedules, and stakeholder communications
Coordinate document workflows and maintain organized project records
Prepare presentations, reports, agendas, and executive communications
Capture and distribute accurate meeting minutes and action items
Support procurement tracking, travel coordination, and team logistics

Lead cross‑functional collaboration, resolving issues and strengthening alignment across the organization

Interested? For this role we’re looking for the following education, experience, and skills
Minimum requirements

High School Diploma Required
Experience supporting complex projects and senior leadership
Strong organizational skills with attention to detail and confidentiality
Ability to manage multiple priorities and meet tight deadlines
Strong written and verbal communication skills across teams
Experience collaborating with cross‑functional and external partners
Strong proficiency with Microsoft Office, Teams, PowerPoint and Outlook
Experience using artificial intelligence

Preferred qualifications

Experience in pharmaceutical, healthcare, or regulated industries

Ability to work independently with minimal direction
Experience supporting international teams and travel coordination
Experience with expense reporting and budget tracking tools
Exceptional attention to detail and accuracy
Experience using Microsoft Visio
Bachelor's Degree

This positions reasonably anticipated base salary range is $63,200-83,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Clinical Account Specialist HS - Seattle (Seattle, Washington, US)

Make your mark for patients

To strengthen our Dermatology HS Sales Team, we are looking for a talented individual to join our Field Based team in the position of: Clinical Account Specialist HS – Seattle, WA.

The Clinical Account Specialist (CAS) position is responsible for driving demand for the current and future Dermatology pipeline assets in an assigned territory. Reinforcing the clinical features of the product, engaging and building relationships with clinical decision makers and office support staff, and working in concert with the broader UCB organization to create the best experiences for patients living with severe immunologic diseases.

About the role:

Develop a strong understanding and awareness of the patient journey of care, including taking responsibility for ensuring needed therapies get to the patient.
Offer an outstanding patient experience with our product by communicating clinical information on dermatology products and relevant patient support services to an audience of health care professionals and office staff.
Establish an understanding of the local health care ecosystems, including the payor environment.
Demonstrate the UCB Patient Value Strategy principles by establishing collaborative and team-oriented working relationships and integrating within a matrix environment.
Behave compliantly with all UCB policies / approved messages and coach the team to use of approved UCB sales materials and messages with HCPs and other external stakeholders.

What you’ll do:

Owning responsibility for attaining territory sales goals and objectives through effective territory planning, visiting clinical decision makers with appropriate reach/frequency, collaborating with the Immunology Clinical Specialist and other members of the UCB Patient Value Team.
Analyzing territory data to build and adapt a customer call plan to establish professional working relationships with HCP and support staff.
Maintaining a thorough understanding of the competitive marketplace and drivers of prescriber decisions.
Conducting account related activities such as profiling, call planning, and reviewing UCB sales data with assigned stakeholders.
Making strategic business decisions in the management of allocated resources such as financial/budgets, samples, access opportunities.
Coordinating and supporting promotional educational opportunities and programs intended to expand the knowledge of medical stakeholders and staff (e.g., peer-to-peer educational opportunities) in accordance with UCB policy.

Interested? For this position you’ll need the following education, experience and skills:

Minimum Qualifications:

Bachelor’s Degree BA/BS
Minimum of 3 years of direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry
Must have a valid Driver License with no more than 2 moving violations in the previous three-year period
Must reside within assigned geography

Preferred Qualifications:

5 years of direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry

Experience calling on Dermatologists in the assigned geography
Experience selling injectable biologics products
Proven track record of success in Pharmaceutical Sales demonstrated by goal attainment and awards achievement (President’s Club, etc.)
Biologic product launch experience
Demonstrated business and strategic planning skills to identify unique selling opportunities and adaptability to changing market conditions
Demonstrated understanding of managed care landscape and how it influences/impacts business
Strong verbal, influencing, presentation and written communication skills
Strong collaboration skills and success working in teams

This positions reasonably anticipated base salary range is $132,000 to $174,000 per year. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Clinical Account Specialist HS - Cleveland (Cleveland, Ohio, US)

Make your mark for patients

To strengthen our Dermatology HS Sales Team, we are looking for a talented individual to join our Field Based team in the position of: Clinical Account Specialist HS– Cleveland, OH.

About the role:

Develop a strong understanding and awareness of the patient journey of care, including taking responsibility for ensuring needed therapies get to the patient.
Offer an outstanding patient experience with our product by communicating clinical information on dermatology products and relevant patient support services to an audience of health care professionals and office staff.
Establish an understanding of the local health care ecosystems, including the payor environment.
Demonstrate the UCB Patient Value Strategy principles by establishing collaborative and team-oriented working relationships and integrating within a matrix environment.
Behave compliantly with all UCB policies / approved messages and coach the team to use of approved UCB sales materials and messages with HCPs and other external stakeholders.

What you’ll do:

Owning responsibility for attaining territory sales goals and objectives through effective territory planning, visiting clinical decision makers with appropriate reach/frequency, collaborating with the Immunology Clinical Specialist and other members of the UCB Patient Value Team.
Analyzing territory data to build and adapt a customer call plan to establish professional working relationships with HCP and support staff.
Maintaining a thorough understanding of the competitive marketplace and drivers of prescriber decisions.
Conducting account related activities such as profiling, call planning, and reviewing UCB sales data with assigned stakeholders.
Making strategic business decisions in the management of allocated resources such as financial/budgets, samples, access opportunities.
Coordinating and supporting promotional educational opportunities and programs intended to expand the knowledge of medical stakeholders and staff (e.g., peer-to-peer educational opportunities) in accordance with UCB policy.

Interested? For this position you’ll need the following education, experience and skills:

Minimum Qualifications:

Bachelor’s Degree BA/BS
Minimum of 3 years of direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry
Must have a valid Driver License with no more than 2 moving violations in the previous three-year period
Must reside within assigned geography

Preferred Qualifications:

5 years of direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry

Experience calling on Dermatologists in the assigned geography
Experience selling injectable biologics products
Proven track record of success in Pharmaceutical Sales demonstrated by goal attainment and awards achievement (President’s Club, etc.)
Biologic product launch experience
Demonstrated business and strategic planning skills to identify unique selling opportunities and adaptability to changing market conditions
Demonstrated understanding of managed care landscape and how it influences/impacts business
Strong verbal, influencing, presentation and written communication skills
Strong collaboration skills and success working in teams

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Account Executive / Boston (Boston, Massachusetts, US)

Make your mark for patients

To strengthen and support our launches within US Rare Disease Organization (RDO), we are seeking an Account Executive - Neuromuscular (AE) for the Boston, MA territory. The AE is an expert on the practices, delivery networks, and patient populations within their territory.

About the Role

Who you’ll work with

Call plan physicians/HCPs and all care team members
Sales management/leadership
Market Access, Thought Leader Liaison, and Medical Teams
KOLs
Sites of care

What you’ll do

Consistently exceed territory sales objectives while operating with the highest level of ethics and integrity
Create and execute strategic business plans reflecting a thorough understanding of the local market conditions
Master targeted disease states, which include a deep understanding of patient journeys, standards of care, and treatment drivers
Advocate for Rare Disease patients and serve as the authority on the various tools and resources UCB offers to support physicians, pharmacists, and other health care providers
Continuously expand the expertise of all treating and referring physicians, as well as payers, hospital systems, pharmacies, labs, and other components of the care continuum; maintain awareness and remain attentive to the dynamics between different stakeholders that influence patient treatment decisions
Maintain strong relationships within the payer landscape to ensure providers are informed on coverage and reimbursement status; collaborate with the payer access team to ensure all relevant stakeholders are working with the most up-to-date information to maximize access and affordability for patients using UCB products
Foster strong relationships with patient advocacy groups and partners to support appropriate patient education and disease state awareness activities in the community
Collaborate cross-functionally with UCB colleagues to share insights on customer needs and market opportunities; work together towards more effective approaches to patient value creation
Maintain a commitment to continuous improvement (embrace a growth mindset) as evidenced by insights gained/shared about geography, stakeholders, and customer needs through day-to-day experience; growth in core competencies with feedback sought from managers and colleagues, courses taken, on-the-job projects and relevant periodicals/readings

Our 4 Pillars in Rare Disease Organization

Demonstrate great commitment to the Rare Disease patient community and understand the patient journey, the barriers they face in care and treatment, and how to help them overcome those barriers

Utilize innovative methods to identify patients who need treatment
Maintain a highly tactical approach to patient access
Help patients and caregivers navigate the Healthcare System and work around roadblocks

Interested? For this position, you’ll need the following education, experience, and skills:

Minimum Qualifcations:

Bachelor’s Degree
8+ years of field-based experience in sales, account management, and/or field reimbursement in biopharmaceuticals or healthcare, inclusive of 5+ years in a competitive specialty market segment
Field experience with Buy-and-Bill medical benefits, Specialty Pharmacy, and HUB delivery models
Verifiable record of sustained high sales performance and achievement in top 30% nationally
Experience/involvement in successful product launches
The ability to maximize impact of multichannel/digital tools and strategy/tactics with territory HCPs
Command of key medical, scientific, and healthcare concepts, language, and practices related to neurology and rare diseases
Experience serving a variety of call points – academic centers, community-based care, hospitals, and private office practices
Comfortable spending up to 60% of time traveling with overnight travel required (territory business need dependent)

Preferred experience

2+ years in rare/orphan drug experience in a competitive market
Significant CNS/neuroscience sales experience (to include epilepsy); Oncology, Hematology and/or Specialty reimbursement products requiring Specialty Pharmacy knowledge and expertise
Experience in supporting biologic therapy administered by a designated health care provider
Promotional product experience with REMS requirements

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Account Executive / Boston Sr. (Boston, Massachusetts, US)

Make your mark for patients

To strengthen and support our launches within US Rare Disease Organization (RDO), we are seeking an Account Executive - Neuromuscular (AE) for the Boston, MA Sr. territory. The AE is an expert on practices, delivery networks, and patient populations within their territory.

About the Role

Who you’ll work with

Call plan physicians/HCPs and all care team members
Sales management/leadership
Market Access, Thought Leader Liaison, and Medical Teams
KOLs
Sites of care

What you’ll do

Consistently exceed territory sales objectives while operating with the highest level of ethics and integrity
Create and execute strategic business plans reflecting a thorough understanding of the local market conditions
Master targeted disease states, which include a deep understanding of patient journeys, standards of care, and treatment drivers
Advocate for Rare Disease patients and serve as the authority on the various tools and resources UCB offers to support physicians, pharmacists, and other health care providers
Continuously expand the expertise of all treating and referring physicians, as well as payers, hospital systems, pharmacies, labs, and other components of the care continuum; maintain awareness and remain attentive to the dynamics between different stakeholders that influence patient treatment decisions
Maintain strong relationships within the payer landscape to ensure providers are informed on coverage and reimbursement status; collaborate with the payer access team to ensure all relevant stakeholders are working with the most up-to-date information to maximize access and affordability for patients using UCB products
Foster strong relationships with patient advocacy groups and partners to support appropriate patient education and disease state awareness activities in the community
Collaborate cross-functionally with UCB colleagues to share insights on customer needs and market opportunities; work together towards more effective approaches to patient value creation
Maintain a commitment to continuous improvement (embrace a growth mindset) as evidenced by insights gained/shared about geography, stakeholders, and customer needs through day-to-day experience; growth in core competencies with feedback sought from managers and colleagues, courses taken, on-the-job projects and relevant periodicals/readings

Our 4 Pillars in Rare Disease Organization

Demonstrate great commitment to the Rare Disease patient community and understand the patient journey, the barriers they face in care and treatment, and how to help them overcome those barrier
Utilize innovative methods to identify patients who need treatment
Maintain a highly tactical approach to patient access
Help patients and caregivers navigate the Healthcare System and work around roadblocks

Interested? For this position, you’ll need the following education, experience, and skills:

Minimum Qualifcations:

Bachelor’s Degree
8+ years of field-based experience in sales, account management, and/or field reimbursement in biopharmaceuticals or healthcare, inclusive of 5+ years in a competitive specialty market segment
4+ years of Rare Disease experience in pharmaceuticals/Biologics Field experience with Buy-and-Bill medical benefits, Specialty Pharmacy, and HUB delivery models
Verifiable record of sustained high sales performance and achievement in top 30% nationally
Experience/involvement in successful product launches
The ability to maximize impact of multichannel/digital tools and strategy/tactics with territory HCPs
Command of key medical, scientific, and healthcare concepts, language, and practices related to neurology and rare diseases
Experience serving a variety of call points – academic centers, community-based care, hospitals, and private office practices
Comfortable spending up to 60% of time traveling with overnight travel required (territory business need dependent)

Preferred experience

Significant CNS/neuroscience sales experience (to include epilepsy); Oncology, Hematology and/or Specialty reimbursement products requiring Specialty Pharmacy knowledge and expertise
Experience in supporting biologic therapy administered by a designated health care provider
Promotional product experience with REMS requirements

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Outcomes Liaison, Central (Dallas, Texas, US)

Make your mark for patients

We are seeking a Medical Outcomes Liaison (MOL), Central to serve as a key scientific partner within our US Medical Affairs Epilepsy and Rare Syndromes team. This field‑based role focuses on building strong relationships with decisionmakers, delivering clinical and economic value, and identifying strategic opportunities that positively impact patients living with Epilepsy and Rare Syndromes. This territory covers AL, AR, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, ND, NE, OH, OK, SD, TN, TX, WI.

Candidates must reside within the territory and live near a hub airport in the territory.

Up to 75% of travel required, including overnights and some weekends.

About the Role

The Medical Outcomes Liaison (MOL) provides clinical insights, Health Economics and Outcomes Research (HEOR) expertise, and real‑world evidence to external stakeholders including integrated delivery networks (IDNs), large medical groups, top‑tier research institutions, and regional payers. You will cultivate high‑value partnerships, assess data gaps, and drive field‑based research collaborations to support strategic medical initiatives.

What You’ll Do

Lead execution of the Epilepsy & Rare Syndromes outcomes and RWE engagement strategy across key accounts.
Build and maintain relationships with C‑suite stakeholders, researchers, and payer decision‑makers.
Identify and develop institutional data opportunities that align with strategic evidence needs.
Support field‑based research collaborations and HEOR data generation.
Serve as an expert communicator delivering clinical and economic value propositions across settings of care.
Partner cross‑functionally to address clinical and HEOR data needs at key accounts.

Who you’ll work with

Senior healthcare leaders, including C‑suite and D‑suite decision‑makers within large medical groups, to support high‑level strategic engagements.
Top‑tier research institutions to advance scientific and outcomes‑focused initiatives.
Pharmacy and medical directors at regional payers, providing clinical and economic insights that inform access and value discussions.
Integrated delivery networks (IDNs) and large medical groups to drive outcomes‑ and RWE‑aligned strategies.
Internal cross‑functional partners—regional business units, marketing, sales, medical affairs, and corporate functions—to ensure coordinated execution across the organization.

Interested? For this role we’re looking for the following education, experience, and skills

Minimum Qualifications

Clinically focused graduate degree (MPH, NP, PA). Doctorate degree (PharmD, MD, DO, PhD, DNP) preferred.
Doctoral candidates: Minimum 8 years industry experience + 3 years HEOR/RWE/Outcomes experience.
Non‑doctoral candidates: Minimum 10 years industry experience + 5 years HEOR/RWE/Outcomes experience.

Preferred Qualifications

Doctorate preferred (PharmD, MD, DO, PhD); non‑doctoral clinicians considered with relevant expertise.
Strong background in external stakeholder engagement and decisionmaker relationship management.
Ability to analyze clinical and HEOR data gaps and deliver meaningful solutions.

This position's reasonably anticipated salary range is $156,000-$238,400 annually. The actual salary offered will consider internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Outcomes Liaison, Central (Nashville, Tennesee, US)

Make your mark for patients

Candidates must reside within the territory and live near a hub airport in the territory.

Up to 75% of travel required, including overnights and some weekends.

About the Role

What You’ll Do

Lead execution of the Epilepsy & Rare Syndromes outcomes and RWE engagement strategy across key accounts.
Build and maintain relationships with C‑suite stakeholders, researchers, and payer decision‑makers.
Identify and develop institutional data opportunities that align with strategic evidence needs.
Support field‑based research collaborations and HEOR data generation.
Serve as an expert communicator delivering clinical and economic value propositions across settings of care.
Partner cross‑functionally to address clinical and HEOR data needs at key accounts.

Who you’ll work with

Senior healthcare leaders, including C‑suite and D‑suite decision‑makers within large medical groups, to support high‑level strategic engagements.
Top‑tier research institutions to advance scientific and outcomes‑focused initiatives.
Pharmacy and medical directors at regional payers, providing clinical and economic insights that inform access and value discussions.
Integrated delivery networks (IDNs) and large medical groups to drive outcomes‑ and RWE‑aligned strategies.
Internal cross‑functional partners—regional business units, marketing, sales, medical affairs, and corporate functions—to ensure coordinated execution across the organization.

Interested? For this role we’re looking for the following education, experience, and skills

Minimum Qualifications

Clinically focused graduate degree (MPH, NP, PA). Doctorate degree (PharmD, MD, DO, PhD, DNP) preferred.
Doctoral candidates: Minimum 8 years industry experience + 3 years HEOR/RWE/Outcomes experience.
Non‑doctoral candidates: Minimum 10 years industry experience + 5 years HEOR/RWE/Outcomes experience.

Preferred Qualifications

Doctorate preferred (PharmD, MD, DO, PhD); non‑doctoral clinicians considered with relevant expertise.
Strong background in external stakeholder engagement and decisionmaker relationship management.
Ability to analyze clinical and HEOR data gaps and deliver meaningful solutions.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head of Reward & Talent Operations US (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Head of Reward and HR Operations (US) who is strategic, delivery‑focused, and digitally curious to join us in our Talent & Reward Operations team, based in our UCB office in Atlanta, GA

About the role

In this senior leadership role, you will be accountable for the end‑to‑end reward and HR operations agenda in the United States, UCB’s largest market. You will ensure reliable delivery of core people processes while shaping and implementing a future‑focused reward and HR operating model. The role balances operational excellence, regulatory compliance, and employee experience, while supporting growth, transformation, and integration activities across the US business.

Who you’ll work with

You will work closely with US HR business partners, senior business leaders, and functional teams, including Finance, Legal, IT, and Global HR. You will also collaborate with global reward experts and HR operations leaders to ensure global frameworks are applied consistently and effectively in the US context. As part of the US HR leadership community, you will act as a trusted advisor on reward and HR operations topics.

What you’ll do

Lead US reward and HR operations with reliable execution and strong service quality
Serve as a strategic partner to the Global Head, ensuring US market needs influence and reflect the broader global people strategy
Drive the adoption of global HR operating standards within the US while maintaining the agility required for a high-growth company.
Prepare and present US-specific compensation and benefits data for US leadership review
Ensure regulatory compliance, governance, and effective risk management
Oversee compensation, incentives, benefits, and employee lifecycle processes
Implement simplified, scalable, and digitally enabled reward solutions
Use data and insights to improve decision‑making and employee experience
Build, develop, and engage a high‑performing operational team

Interested? For this role we’re looking for the following

Minimum requirements

Bachelor’s degree in HR, business, finance, or related field
15+ years’ experience in reward, total rewards, or HR operations
Deep knowledge of US compensation, incentives, benefits, and employment practices
Demonstrated ability to influence global stakeholders and navigate cross-cultural organizational dynamics.
Expertise in harmonizing local US compensation, benefits and pay equity standards within global governance frameworks.
Experience working in complex, matrixed, global organizations
Exceptional relationship management skills, with demonstrated ability to build, manage, and sustain strong relationships with senior business leaders and other stakeholders
Exposure to organizational growth, restructuring, and M&A activities
Ability to translate complex data sets into actionable business insights for executive-level decision-making.

Preferred requirements

Advanced degree in HR, business, or a related discipline
SHRM-CP or SHRM-SCP Certification
Experience driving HR reward transformation and digital enablement
Experience in biopharma or a related regulated industry

This positions reasonably anticipated base salary range is $236,800 - $310,800. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Omnichannel & Digital Marketing Lead - Next Best Action (NBA) (Atlanta, Georgia, US)

Make your mark for patients

We are looking for an Omnichannel & Digital Marketing Lead - Next Best Action (NBA) to join our Omnichannel & Stakeholder Engagement team based out of either Atlanta, GA or Raleigh, NC (hybrid)

About the role

The Omnichannel Lead is responsible for developing, executing, and evolving Next Best Action (NBA) capabilities to enable seamless omnichannel orchestration across field and digital channels within UCB’s US Enterprise.

Who you’ll work with

This role requires strong strategic leadership and close collaboration with cross-functional teams to design, implement, and scale NBA solutions that drive integration into field activation. The Lead ensures alignment with brand and omnichannel objectives, leveraging data-driven insights to optimize HCP engagement and product adoption. Additional responsibilities include managing vendor relationships, overseeing technical integration (e.g., Veeva), tracking adoption and performance metrics, and fostering a culture of data-driven decision-making and continuous improvement.

What you’ll do

Oversee the execution and scaling of NBA initiatives to enable seamless omnichannel orchestration across field and digital channels across all PVUs, driving customer-centric engagement and measurable business outcomes.
Develop and spearhead multi-year strategic plans and omnichannel portfolio strategies for field force deployment and activation, ensuring alignment with organizational goals and brand vision.
Own the roadmap, execution, and measurement of field activation programs, including the integration of NBA solutions with technical platforms (e.g., Veeva, MDM/CDP), and ensure delivery of scalable, data-driven impact.
Leverage data-driven insights (e.g., engagement, utilization, execution rates) to optimize field performance, content, channels, and tactics, providing actionable recommendations to executive leadership and cross-functional stakeholders.
Evaluate program ROI, sales performance, and execution metrics, delivering clear, impactful updates to stakeholders and supporting future innovation.
Build strategic partnerships with omnichannel, NPP, brand and field technology leaders to align field engagement strategies with brand vision and ensure seamless technical integration.
Manage vendor engagement to ensure NBA and omnichannel solutions meet business needs and support ongoing enhancements.
Act as a change agent to foster a data-driven culture, promoting omnichannel adoption and continuous improvement across teams.
Guide the organization toward integrated, data-driven engagement models by anticipating industry trends, advocating for innovative technologies, and realigning strategies based on performance data and market insights.

Interested? For this role we’re looking for the following education, experience and skills

Required:

Bachelors Degree
10+ years in the pharmaceutical or related industry sales, marketing, field force operations, or omnichannel strategy, with a preference for roles involving NBA or similar data-driven engagement models.

Preferred:

Strong understanding of omnichannel marketing strategies, field and digital channel orchestration, and NBA concepts.
Knowledge of the pharmaceutical industry, HCP behavior, and regulatory compliance
Experience with CRM systems and technical integration and proficiency in data analysis and interpretation (KPIs, engagement rates, sales impact, campaign ROI, etc.).
Proven experience managing vendor relationships and external partners.
Excellent project management, communication, and collaboration skills, with the ability to lead and operate independently in a cross-functional environment. '
Ability to translate strategic plans into operational tactics and align solutions with business objectives.

This positions reasonably anticipated base salary range is $148,000 - $195,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Omnichannel & Digital Marketing Lead - Next Best Action (NBA) (Raleigh, North Carolina, US)

Make your mark for patients

About the role

Who you’ll work with

What you’ll do

Oversee the execution and scaling of NBA initiatives to enable seamless omnichannel orchestration across field and digital channels across all PVUs, driving customer-centric engagement and measurable business outcomes.
Develop and spearhead multi-year strategic plans and omnichannel portfolio strategies for field force deployment and activation, ensuring alignment with organizational goals and brand vision.
Own the roadmap, execution, and measurement of field activation programs, including the integration of NBA solutions with technical platforms (e.g., Veeva, MDM/CDP), and ensure delivery of scalable, data-driven impact.
Leverage data-driven insights (e.g., engagement, utilization, execution rates) to optimize field performance, content, channels, and tactics, providing actionable recommendations to executive leadership and cross-functional stakeholders.
Evaluate program ROI, sales performance, and execution metrics, delivering clear, impactful updates to stakeholders and supporting future innovation.
Build strategic partnerships with omnichannel, NPP, brand and field technology leaders to align field engagement strategies with brand vision and ensure seamless technical integration.
Manage vendor engagement to ensure NBA and omnichannel solutions meet business needs and support ongoing enhancements.
Act as a change agent to foster a data-driven culture, promoting omnichannel adoption and continuous improvement across teams.
Guide the organization toward integrated, data-driven engagement models by anticipating industry trends, advocating for innovative technologies, and realigning strategies based on performance data and market insights.

Interested? For this role we’re looking for the following education, experience and skills

Required:

Bachelors Degree
10+ years in the pharmaceutical or related industry sales, marketing, field force operations, or omnichannel strategy, with a preference for roles involving NBA or similar data-driven engagement models.

Preferred:

Strong understanding of omnichannel marketing strategies, field and digital channel orchestration, and NBA concepts.
Knowledge of the pharmaceutical industry, HCP behavior, and regulatory compliance
Experience with CRM systems and technical integration and proficiency in data analysis and interpretation (KPIs, engagement rates, sales impact, campaign ROI, etc.).
Proven experience managing vendor relationships and external partners.
Excellent project management, communication, and collaboration skills, with the ability to lead and operate independently in a cross-functional environment. '
Ability to translate strategic plans into operational tactics and align solutions with business objectives.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Dermatology APP Medical Liaison - East (Field Based, Field Based, US)

Make your mark for patients

About the role:

As a Dermatology Advanced Practice Provider (APP) Medical Affairs Liaison, you will serve as a key field-based scientific partner to dermatology NPs and PAs, supporting the launch and lifecycle management of innovative therapies for chronic skin conditions such as psoriasis, hidradenitis suppurativa and atopic dermatitis. This role reports into the Medical Affairs organization, ensuring scientific integrity and alignment with UCB’s mission to create value for patients.

Who you’ll work with:

Partnering with Dermatology MSLs, Medical Outcome Liaisons, and other field teams in regional/local projects.
Conducting peer-to-peer scientific discussions with dermatology APPs
Supporting APPs at national/regional congresses and local society meetings
Gathering and communicating actionable insights from the APP community to inform medical strategy
Collaborating with cross-functional teams to ensure alignment and responsiveness to field needs

What you’ll do:

Contributing to territory-level medical plans and educational initiatives
Upholding UCB’s core values and ethical standards in all interactions
Ensuring compliance with all applicable laws, regulations, and internal policies
Extensive travel (up to 70%) required, including overnights and some weekends.
Delivering medical education aligned with UCB’s dermatology portfolio and pipeline

Interested? For this role we’re looking for the following education, experience and skills:

Minimum Education/Experience Requirements:

Bachelor’s degree plus NP/PA Degree (MSN, PA).
5 years clinical experience as a Nurse Practitioner (NP) or Physician Assistant (PA) in dermatology, rheumatology or gastroenterology.
Minimum of 3 years of prior pharmaceutical industry experience
Ability to travel up to 70%, including occasional weekends for conferences

Preferred Requirements:

• Doctorate degree.

• Familiarity with payer landscapes including Medicare, Medicaid, and commercial plans.

• Strong understanding of psoriasis, hidradenitis suppurativa and atopic dermatitis.

Core Competencies:

Clinical credibility and ability to engage in peer-level dialogue
Strategic thinking and insight generation
Collaborative mindset and ability to work cross-functionally
Strong communication and presentation skills
Commitment to compliance and ethical standards

*This position's reasonably anticipated base salary range is $134,000 - $176,000 annually. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills and experience, among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Dermatology APP Medical Liaison - West (Field Based, Field Based, US)

Make your mark for patients

About the role:

Who you’ll work with:

Partnering with Dermatology MSLs, Medical Outcome Liaisons, and other field teams in regional/local projects.
Conducting peer-to-peer scientific discussions with dermatology APPs
Supporting APPs at national/regional congresses and local society meetings
Gathering and communicating actionable insights from the APP community to inform medical strategy
Collaborating with cross-functional teams to ensure alignment and responsiveness to field needs

What you’ll do:

Contributing to territory-level medical plans and educational initiatives
Upholding UCB’s core values and ethical standards in all interactions
Ensuring compliance with all applicable laws, regulations, and internal policies
Extensive travel (up to 70%) required, including overnights and some weekends.
Delivering medical education aligned with UCB’s dermatology portfolio and pipeline

Interested? For this role we’re looking for the following education, experience and skills:

Minimum Education/Experience Requirements:

Bachelor’s degree plus NP/PA Degree (MSN, PA).
5 years clinical experience as a Nurse Practitioner (NP) or Physician Assistant (PA) in dermatology, rheumatology or gastroenterology.
Minimum of 3 years of prior pharmaceutical industry experience
Ability to travel up to 70%, including occasional weekends for conferences

Preferred Requirements:

• Doctorate degree.

• Familiarity with payer landscapes including Medicare, Medicaid, and commercial plans.

• Strong understanding of psoriasis, hidradenitis suppurativa and atopic dermatitis.

Core Competencies:

Clinical credibility and ability to engage in peer-level dialogue
Strategic thinking and insight generation
Collaborative mindset and ability to work cross-functionally
Strong communication and presentation skills
Commitment to compliance and ethical standards

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Outcomes Liaison, West (Phoenix, Arizona, US)

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We are seeking a Medical Outcomes Liaison (MOL), West to serve as a key scientific partner within our US Medical Affairs Epilepsy and Rare Syndromes team. This field‑based role focuses on building strong relationships with decisionmakers, delivering clinical and economic value, and identifying strategic opportunities that positively impact patients living with Epilepsy and Rare Syndromes. This territory covers AK, AZ, CA, CO, HI, ID, MT, NM, NV, OR, UT, WA, WY.

Candidates must reside within the territory and live near a hub airport in the territory.

Up to 75% of travel required, including overnights and some weekends.

About the Role

What You’ll Do

Lead execution of the Epilepsy & Rare Syndromes outcomes and RWE engagement strategy across key accounts.
Build and maintain relationships with C‑suite stakeholders, researchers, and payer decision‑makers.
Identify and develop institutional data opportunities that align with strategic evidence needs.
Support field‑based research collaborations and HEOR data generation.
Serve as an expert communicator delivering clinical and economic value propositions across settings of care.
Partner cross‑functionally to address clinical and HEOR data needs at key accounts.

Who you’ll work with

Senior healthcare leaders, including C‑suite and D‑suite decision‑makers within large medical groups, to support high‑level strategic engagements.
Top‑tier research institutions to advance scientific and outcomes‑focused initiatives.
Pharmacy and medical directors at regional payers, providing clinical and economic insights that inform access and value discussions.
Integrated delivery networks (IDNs) and large medical groups to drive outcomes‑ and RWE‑aligned strategies.
Internal cross‑functional partners—regional business units, marketing, sales, medical affairs, and corporate functions—to ensure coordinated execution across the organization.

Interested? For this role we’re looking for the following education, experience, and skills

Minimum Qualifications

Clinically focused graduate degree (MPH, NP, PA). Doctorate degree (PharmD, MD, DO, PhD, DNP) preferred.
Doctoral candidates: Minimum 8 years industry experience + 3 years HEOR/RWE/Outcomes experience.
Non‑doctoral candidates: Minimum 10 years industry experience + 5 years HEOR/RWE/Outcomes experience.

Preferred Qualifications

Doctorate preferred (PharmD, MD, DO, PhD); non‑doctoral clinicians considered with relevant expertise.
Strong background in external stakeholder engagement and decisionmaker relationship management.
Ability to analyze clinical and HEOR data gaps and deliver meaningful solutions.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Outcomes Liaison, West (Seattle, Washington, US)

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Candidates must reside within the territory and live near a hub airport in the territory.

Up to 75% of travel required, including overnights and some weekends.

About the Role

What You’ll Do

Lead execution of the Epilepsy & Rare Syndromes outcomes and RWE engagement strategy across key accounts.
Build and maintain relationships with C‑suite stakeholders, researchers, and payer decision‑makers.
Identify and develop institutional data opportunities that align with strategic evidence needs.
Support field‑based research collaborations and HEOR data generation.
Serve as an expert communicator delivering clinical and economic value propositions across settings of care.
Partner cross‑functionally to address clinical and HEOR data needs at key accounts.

Who you’ll work with

Senior healthcare leaders, including C‑suite and D‑suite decision‑makers within large medical groups, to support high‑level strategic engagements.
Top‑tier research institutions to advance scientific and outcomes‑focused initiatives.
Pharmacy and medical directors at regional payers, providing clinical and economic insights that inform access and value discussions.
Integrated delivery networks (IDNs) and large medical groups to drive outcomes‑ and RWE‑aligned strategies.
Internal cross‑functional partners—regional business units, marketing, sales, medical affairs, and corporate functions—to ensure coordinated execution across the organization.

Interested? For this role we’re looking for the following education, experience, and skills

Minimum Qualifications

Clinically focused graduate degree (MPH, NP, PA). Doctorate degree (PharmD, MD, DO, PhD, DNP) preferred.
Doctoral candidates: Minimum 8 years industry experience + 3 years HEOR/RWE/Outcomes experience.
Non‑doctoral candidates: Minimum 10 years industry experience + 5 years HEOR/RWE/Outcomes experience.

Preferred Qualifications

Doctorate preferred (PharmD, MD, DO, PhD); non‑doctoral clinicians considered with relevant expertise.
Strong background in external stakeholder engagement and decisionmaker relationship management.
Ability to analyze clinical and HEOR data gaps and deliver meaningful solutions.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Learning Manager (Atlanta, Georgia, US)

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We are looking for a Learning Manager – US Neurology with experience in sales, implementing and coordinating learning projects, marketing, and facilitation to join our US Learning & Development Team. This hybrid role is based in our U.S. Headquarters Office in Smyrna, GA.

About the role

You will act as an outstanding course facilitator. Delivering learning experiences that inspire, build competencies, and improve individual's and team’s performance. You will be responsible for keeping up to date with and rapidly implementing the latest trends and methods in learning delivery. You will lead the content development process either by self-development or orchestrating with external partners to ensure deliverables align with stakeholder strategy in the execution of continuous skill development and facilitation of material.

Who you’ll work with

You will partner with key internal customers (learner) regarding new hire training, launch preparation, PIM planning/execution and pull-through.

What you’ll do

Engage and elicit interactions from participants to successfully lead them to attain learning outcomes during blended learning experiences: face-to-face, virtual sessions
Maintain communication with learners for the duration of the course/module
Utilize learning systems to monitor, track, and report learning activities – attendance, performance, learner feedback
Oversee the learning environment for classroom setup, course materials, media and co-facilitator coordination.
Operate with a business owner mindset identifying if content is currently available, can be built internally, or requires external partner assistance
Select and negotiate with appropriate external partners
Own end to end development and delivery of aligned content
Remain current and proficient on business and technological evolutions, (including scientific knowledge) course materials, and facilitation best practice, methods and trends
Gather and monitor feedback on content, facilitation and the learning experiences and outcomes.
Propose innovative solutions based on learning and development expertise, provide insight based on information gathered, and give feedback to the Learning and Development Team for continuous improvement of competency expertise
Establish and maintain contacts with people throughout the UCB Learning Function and share best practice knowledge and experience with them to improve facilitation expertise and learning quality throughout the organization

Interested? For this role we’re looking for the following education, experience and skills

Minimum:

Bachelor’s Degree in Business, Human Resources, Business, Education, Organizational Psychology, Business or experience equivalent.
3-5+ years’ experience in in pharmaceutical/Biotech industry with preference in the Neurology/Epilepsy space.

Preferred:

Experience in sales, implementing and coordinating learning projects, marketing, and facilitation is a plus.
Experience working with content creation platforms as a tool for creating, managing, and delivery of training content as well as SharePoint, Microsoft Teams, Microsoft 365, AI platforms and Vyond.

This positions reasonably anticipated base salary range is $108,000-141,800. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Science Liaison Dermatology - NYC (New York, New York, US)

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About the role

The Medical Science Liaison (MSL) is a professional who serves as a key field-based scientific partner to healthcare providers and decision-makers, medical professional associations, and internal UCB colleagues. This professional will be responsible for executing key medical strategies to enhance and positively impact patients living with chronic inflammatory diseases.

Who you will work with:

This position will support our Immunology Patient Value Unit (PVU) in an assigned geography of New York City.

What you’ll do:

Maintain deep scientific knowledge in areas of Dermatology while delivering clinical value propositions and engages with key decision-maker stakeholders in medical groups, IDNs, and regional payers
Identifies and supports potential research expansion projects/collaborations, medical advisors, and educational partnership opportunities
Conducts local roundtables and education programs that aim enhance Key Opinion Leaders (KOL)s understanding of unmet clinical needs
Serve as a scientific expert at key medical and scientific conferences, advisory boards, clinical investigator meetings, and internal meetings.
Supports field-based cross-functional teams to provide medical expertise in access engagements as needed as well as provide field updates regarding topics of interest for creation and/or updating of Standard Response Letters
Reviews and critiques scientific publications to help inform healthcare trends in Dermatology
Collects, analyzes, and communicates information concerning therapeutic area, treatment options, emerging standards of care, and competitive intelligence as well as addresses medical information inquiries
Provides effective clinical presentations to internal and external audiences and tailors presentations to meet specific audience needs through peer to peer scientific exchange
Assesses feasibility and serves as the primary liaison between UCB and investigator for unsolicited Investigator-Initiated Studies (IISs) from inception to publication

Interested? For this role we’re looking for the following education, experience and skills

Minimum Requirements:

Doctorate degree (PharmD, MD, DO or PhD in a relevant field) required.
Valid US Driver’s License and with no more than 3 moving violations in the past 2 years
Must reside within the assigned territory
Must complete initial training and successfully pass all assessments within 90 days of hire

Frequent business travel required, including overnights and some weekends.

Preferred Requirements:

3+ years of field medical experience preferred.
Immuno-dermatology experience strongly preferred. Prior product launch experience also preferred.
Basic business acumen with a solid understanding of the pharmaceutical industry
Basic knowledge and understanding of health economic principles and clinical trials
Ability to clearly articulate complex scientific concepts in 1:1 and group settings
Strong interpersonal skills and excellent verbal and written communication skills
Creative approach to problems solving and able to work effectively in a constantly changing environment
Must be a strong team player and effectively interface with other internal departments including regional business units, marketing, sales, medical affairs, and clinical operations
Strong time management, and organizational skills with proficiency in Microsoft applications

*This position's reasonably anticipated base salary range is $156,000 - $204,000 annually. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills and experience, among other factors and may fall outside the expected range

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Scientist I/II - In Vitro Pharmacology (Cambridge, Massachusetts, US)

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Position: Scientist I/II – In Vitro Pharmacology

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We are seeking an experienced Scientist to join our U.S. In Vitro Pharmacology group based in Cambridge, MA . This is a lab-based function and will support early research projects across UCB’s therapeutic areas of interest through the development, execution, and evaluation of biochemical and biophysical assays.

About the role

You will contribute to early-stage research programs by developing, executing, and interpreting biochemical and biophysical assays. You will support drug discovery projects across therapeutic areas while collaborating with cross-functional partners.

Who you’ll work with

You will work within a multidisciplinary in vitro pharmacology team and collaborate with scientists across research functions to advance discovery programs.

What you’ll do

Develop and perform biochemical and biophysical assays to evaluate or confirm compound MoAs
Achieve drug project milestones and deliver on objectives through effective internal collaboration
Drive scientific excellence and technology developments to maximize both current and future impact on cross-functional teams, programs, and projects
Provide strong scientific thinking, communication, and enhance scientific learnings on multiple projects

Interested? For this role we’re looking for the following minimum requirements:

Minimum requirements

Biochemist/biophysicist with BS + 8, MS +4, or PhD +0-2 years of applicable research experience
Experience in characterization of small molecule-protein and protein-protein interactions
Familiarity with biochemical/biophysical methods including SPR, fluorescence spectroscopy, and DEL screening
Proficiency in common data analysis principles
Strong communicator with excellent presentation and organizational skills
Independent scientist who can drive projects with minimal supervision but also thrive in a multidisciplinary team environment

Preferred qualifications

Industry/biotech focused experience with small molecules/ligands/therapeutics preferred.

Experience with targeted protein degradation, the ubiquitin proteasome system, and/or E3 ligase biology are a plus.
Experience in neuromuscular biology, muscle biology, neuroscience, or immunology is a plus.

Familiarity with medium to high throughput screening and automation is preferred.

This position’s reasonably anticipated base salary range is $99,200 To $130,200 per year. The actual salary offered will consider internal equity and may also vary depending on the candidate’s region, job-related knowledge, skills and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Enablement Lead, Atlanta, GA (Atlanta, Georgia, US)

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We are seeking a Medical Enablement Lead to elevate and streamline execution across the US Medical Team supporting Epilepsy & Rare Syndromes (EaRS). In this strategic role, you will strengthen cross‑portfolio impact by optimizing processes, systems, and collaboration across the medical organization.

About the role

As the Medical Enablement Lead, you will be a pivotal connector within the US Medical EaRS organization—aligning medical strategic planning with field execution to ensure operational excellence. You’ll enhance team efficiency, optimize digital platforms including CRM and content systems, and drive cohesive execution of key medical initiatives. This role partners deeply across field medical, global medical, operations, analytics, and digital/IT teams to deliver high‑quality, compliant, and scalable medical operations.

What You’ll Do

Manage the overall process for national conferences.
Identify, develop, implement, and integrate systems and solutions with impacts across the portfolio, such as Veeva Medical Insights.
Lead internal process for field-based projects originated from Medical Science Liaison (MSL) and Medical Outcome Liaison (MOL) in EaRS.

Identify system and platform needs that integrate medical strategic planning with field execution, including KPI and insights implementation, tracking, and reporting.
Implement processes, procedures, and systems to ensure operational excellence across the EaRS product portfolio.
Collaborate with global medical communities to identify and implement best practices within the US EaRS team.
Provide operational leadership across projects through influence.
Partner with Field Team leaders to drive updates to Field Team CRM and View360.
Ensure executional excellence through effective use of internal digital assets and content management systems.

Who you’ll work with

US Medical EaRS leadership and cross-portfolio medical strategy partners.
Field Medical leaders, including Medical Science Liaison (MSL) and Medical Outcome Liaison (MOL) teams.
Commercial and Market Access partners to align execution with compliant customer engagement.
Medical Operations, Insights/Analytics, and Digital/IT teams to enable KPI tracking, CRM (e.g., View360) updates, and content governance.
External vendors and congress logistics partners to deliver meeting planning and execution.

Interested? For this position you’ll need the following education, experience and skills:

Minimum Qualifications:

Master’s degree.

Minimum of 10 years(non-doctoral) or 5 years (doctoral) biopharmaceutical experience.

Preferred Qualifications:

Deep understanding of operations and processes in medical affairs.
Track record of cross-functional collaboration and excellent project management skills.
Experience in contracting, negotiation, vendor management expertise and system implementation.

High ethics and compliance awareness.

This position's reasonably anticipated salary range is $148k-$194k annually. The actual salary offered will consider internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head of Global RWE and HEOR Strategy - Immunology(ATL) (Atlanta, Georgia, US)

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We are looking for a Head of Global RWE and HEOR Strategy – Immunology who is strategic, scientifically rigorous, and future‑focused to join us in our Immunology team, based in our office on Atlanta, GA, Raleigh, NC or Boston, MA.

About the role

You will define and lead the global data and evidence strategy for our immunology portfolio, shaping how real‑world data and health economics evidence support development and lifecycle decisions. You will anticipate future evidence needs, ensure scientific excellence, and translate complex data into clear insights that inform regulatory, payer, medical, and commercial decision‑making. You will also represent the organization externally and build partnerships that enhance the credibility and impact of our evidence.

Who you’ll work with

You will be working in a highly transversal environment alongside asset teams, health economics and outcomes research experts, digital and analytics specialists, and senior enterprise stakeholders. You will lead and develop a global team of evidence professionals while collaborating closely with internal centers of excellence and external partners to deliver innovative, fit‑for‑purpose evidence strategies.

What you’ll do

• Define and lead global real‑world evidence and health economics strategies
• Anticipate future evidence needs to support development and lifecycle decisions
• Translate complex data landscapes into actionable strategic insights
• Ensure scientific rigor across evidence generation methodologies
• Lead and develop high‑performing global evidence teams
• Represent the organization in external scientific, payer, and regulatory forums

Interested? For this role we’re looking for the following

Minimum requirements

• Advanced degree in health sciences, economics, epidemiology, or related field
• 10+ years’ experience in real‑world evidence or health economics leadership
• 5+ years’ experience defining global evidence strategies across asset lifecycles
• 5+ years’ experience people leadership in complex, matrixed organizations
• Strong knowledge of payer and health technology assessment expectations

Preferred requirements

• Experience in immunology or related therapeutic areas
• Track record of external scientific engagement and partnership building
• Experience applying advanced analytics, machine learning, or AI in evidence generation

This positions reasonably anticipated base salary range is $236,000-310,800. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head of Global RWE and HEOR Strategy - Immunology (BOS) (Boston, Massachusetts, US)

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About the role

Who you’ll work with

What you’ll do

Interested? For this role we’re looking for the following

Minimum requirements

Preferred requirements

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Business Planning & Operations Associate (Atlanta, Georgia, US)

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We are looking for a Business Planning and Operations Associate who is strategic, analytical, and collaborative to join us in our U.S. Corporate Affairs team, based in our office in Atlanta, GA.

About the role

You will play a pivotal role in enabling U.S. Corporate Affairs to operate with clarity, consistency, and impact. As a strategic partner to functional leaders, you will support integrated planning, budgeting, governance, and performance tracking. You will help transform strategy into execution by strengthening ways of working, improving insights, and ensuring operational discipline across the organization.

Who you’ll work with

You will be working in a team that partners closely with Corporate Affairs leadership, Finance, Procurement, Legal, and cross‑functional colleagues. The team is focused on driving alignment, operational excellence, and continuous improvement while supporting meaningful engagement with external stakeholders and advancing organizational priorities.

What you’ll do

Support annual and quarterly planning aligned to Corporate Affairs strategic priorities
Coordinate leadership meetings, agendas, and follow‑up to enable effective decision making
Track initiative progress, risks, and milestones, ensuring accountability and timely escalation
Coordinate budgeting, forecasting, and quarterly reviews with finance partners
Manage vendor contracts, timelines, compliance requirements, and performance tracking
Develop dashboards, reports, and insights to support leadership decision making

Interested? For this role we’re looking for the following

Minimum requirements

Bachelor’s degree in business, finance, sustainability, or related field
5+ of experience in planning, operations, or strategy roles
Demonstrated experience managing budgets, forecasts, and operational processes
Strong analytical, problem‑solving, and structured thinking capabilities
Excellent written and verbal communication skills
Proven ability to collaborate and influence across functions

Preferred requirements

Master’s degree in business, finance, sustainability, or related discipline
Experience in healthcare, biotechnology, pharmaceutical, or related industries
Working knowledge of sustainability principles and performance integration
Experience with enterprise planning, financial, or cloud‑based digital tools
Background supporting senior leaders or enterprise‑wide initiatives

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Executive Assistant (Atlanta, Georgia, US)

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We are looking for an Executive Assistant who is organized, proactive, and detail‑oriented to join our U.S. Corporate Affairs team, based in our Atlanta, GA office.

About the role

As an Executive Assistant, you will provide high‑level administrative and operational support to the Head of U.S. Corporate Affairs. Working with minimal direction, you will help ensure smooth day‑to‑day operations by managing schedules, coordinating meetings, supporting travel and expenses, and assisting with budget tracking and team logistics. This role is ideal for someone who enjoys anticipating needs, taking ownership, and partnering closely with senior leaders.

Who you’ll work with

You will work closely with the Head of U.S. Corporate Affairs and collaborate with cross‑functional internal teams and external partners. The team operates in a fast‑paced, collaborative, and international environment, where accuracy, discretion, and strong communication are essential.

What you’ll do

Provide high‑level administrative support to senior leadership
Manage calendars, schedules, and meeting logistics with minimal supervision
Prepare agendas, minutes, and meeting materials
Coordinate domestic and international meetings and events
Arrange travel and process expense reports
Support onboarding, budgeting, and office coordination activities

Interested? For this role we’re looking for the following

Minimum requirements

Bachelor’s degree required
5+ years of executive or senior administrative assistant experience
5+ years experience supporting senior leaders in complex, fast‑paced environments
Proven ability to manage multiple priorities and meet deadlines
Strong written and verbal communication skills
High level of discretion when handling confidential information

Preferred requirements

Experience in pharmaceutical, healthcare, or regulated industries
Ability to work independently with minimal direction
Experience supporting international teams and travel coordination
Strong proficiency with Microsoft Office, Teams, and Outlook
Experience with expense reporting and budget tracking tools
Exceptional attention to detail and accuracy

This positions reasonably anticipated base salary range is $73,600-$96,600. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Competitive Intelligence Lead, Neurology (Atlanta, Georgia, US)

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We are looking for a Competitive Intelligence Lead join our Integrated Insights, Competitive Intelligence team based out of one of our following hub locations: Brussels, BE - Slough, UK - Atlanta, GA USA

About the role

The Competitive Intelligence Lead will cover the full range of competitive intelligence methodologies, skills and processes, combining CI expertise, with a scientific outlook. This role manages global competitive intelligence initiatives across the portfolio, from early assets to marketed products in our developed brands portfolio, with a main focus on our Neurology portfolio.

Who you’ll work with

The Competitive Intelligence Lead is one of enquiry, innovation and being a thought partner for the competitive environments of the future for our asset teams. This role works closely with other team members and internal stakeholders alike, adding to the continual growth and improvement of our holistic future competitive understanding.

What you’ll do

Effectively manages resources to provide management and other business stakeholders with actionable information and insight regarding competitive intelligence across the portfolio as identified and assigned. This includes on-going deliverables as well as leveraging deep dive methodologies such as war-gaming, scenario planning, conference intelligence gathering, and others.
Ensure consistency with internal Competitive Intelligence colleagues related to use of methodology, systems and tools.
Works closely with Insight Integrators, New Product Planning Leads, Future’s Lead and Head Competitive Intelligence to ensure needs, methodologies, outputs and actions/recommendations are consistent, informative, and future focused across the areas where working.
Utilize well known and innovative solutions from complex problems, provides actionable recommendations, and facilitates delivery and execution of workshops and competitive intelligence programs.
Use scientific and commercial experience to deliver deep and meaningful, actionable insights including in areas where there is some ambiguity.
Monitors the external environment to gain a deeper understanding in competitive intelligence and research techniques and bring those forward within the organization.
Provides holistic insight-driven consultation to all levels of internal stakeholders for the assets in scope for the competitive intelligence.
Executes primary and secondary competitive insights research to clarify issues and reduce risk in decision making for marketed, new, and molecules in development.
Develops with the asset teams and Insight Integrators insights that incorporate an understanding of primary & secondary competitive intelligence, trend watching, and environmental understanding.
Oversees the delivery of objective, independent, and value driven insights gained from both primary and secondary competitive research designed to enable fact-based decision making.
Seeks out, assesses, and recommends innovative insights methodologies, information sources, and vendors.
Assess need and utility of semi-automated, automated algorithms to benefit UCB
Accountability for the knowledge management of CI reporting

Interested? For this role we’re looking for the following education, experience and skills

Required:

Bachelors Degree
2+ years of Competitive Intelligence or related experience in pharmaceuticals or consumer products
Some overnight travel, including internationally, required

Preferred:

Masters Degree or PhD highly preferred
Understanding of competitive intelligence techniques and methodologies, combined with a scientific background which can be brought to bear on the issues facing asset teams, both early, pre-launch and launched
Technical Excellence - Maintains extensive knowledge of the relevant therapy areas, the competitive environment within each area, patient journeys, patient experience and unmet needs, clinical practice, patient access & reimbursement, understanding of how to leverage technology and digital to support UCB brands and strategies, Competitive Intelligence methodologies including congress intelligence, landscaping, dynamic SWOT, PESTEL, Five Forces and Four Corner analysis, primary intelligence project, secondary data analysis, war gaming etc. are included in the Competitive Insights Technical Excellence Competency.
Maintains knowledge of current vendors, potential partners, and methods to complete competitive intelligence projects and advise stakeholders.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Integrated Insights Lead, US Immunology (Atlanta, Georgia, US)

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We are looking for an Integrated Insights Lead, US Immunology to join our Global Integrated Insights team based out of either Atlanta, GA or Raleigh, NC

About the role

The Integrated Insights Lead serves as the primary insights partner for the US Dermatology and Rheumatology business teams. The role is responsible for engaging and translating a wide range of internal and external information – commercial data, market research, analytics, domain expertise, and organizational knowledge – into clear, actionable recommendations that guide UCB’s strategic and operational decisions. The individual must demonstrate strategic thinking, strong analytical acumen, deep understanding of the US immunology landscape, and the ability to influence senior leaders through compelling insight-driven storytelling.

Key elements of the role include:

Delivering integrated insights that support Dermatology and Rheumatology growth plans.
Providing objective recommendations based on holistic analysis of available data
Balancing new research needs with reuse of existing organizational knowledge\
Representing US learnings within global planning processes
Ensuring insights are leveraged consistently and effectively across teams and markets

Who you’ll work with

The role holds matrix leadership accountability for orchestrating how insights are generated, integrated, and communicated across teams. Success depends on strong cross-functional collaboration, proactive information-sharing, and the ability to simplify complexity for diverse stakeholders. The insights lead owns the US product specific insights needs plan, anticipates opportunities, shapes research priorities, and ensures coordination with internal insights partners – including Primary Market Research, Competitive Intelligence, Advanced Analytics, and Insight-to-Impact colleagues. The role also partners closely with regional and global BIMXELX insights leads to ensure alignment and consistent insight narratives across regions.

What you’ll do

Strategic Leadership: Provide strategic insights leadership across the commercial lifecycle of BIMZELX, ensuring decisions are grounded in robust evidence and integrated perspectives.
Cross Functional Collaboration: Drive strong coordination within US BIMZELX insights, across global insights partners, and between other asset teams to maximize efficiency, share best practices, and accelerate impact.
Integrated Insights Execution: Oversee US insight plans, including research, analysis, and analytics priorities, ensuring that workstreams are aligned, well-integrated, and delivered with impact.
Methodological Stewardship: Ensure the right modalities are used for each business question—leveraging datasets, analytics, AI-driven approaches, and existing knowledge before commissioning new work.
Business Partnership: Strengthen relationships with US commercial teams, global partners, Insight Engines, finance, forecasting, and other internal stakeholders.
Insight Delivery: Contribute directly to the creation, analysis, and communication of insights that inform strategic choices.
Market Awareness: Maintain up-to-date understanding of the US immunology market, key competitors, emerging dynamics, and unmet needs.

Interested? For this role we’re looking for the following education, experience and skills

Bachelors Degree
8+ years of relevant experience within pharmaceutical commercial data, market research & analytics
Strong command of commercial and medical data, analytics, advanced analytics, and primary research methodologies.
Deep experience in Rheumatology and Dermatology markets.
Excellent quantitative analysis and interpretation capabilities.
Experience leveraging diverse insight modalities and integrating insights for enriched recommendations.

This positions reasonably anticipated base salary range is $148,000 - 195,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Scientist I or II - Peptide Chemistry (Cambridge, Massachusetts, US)

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We are seeking a motivated new PhD or experienced BS/MS scientist to be an integral member of the Cambridge, MA Chemistry group as a Scientist I or II – Peptide Chemistry, responsible for using our powerful mRNA display peptide discovery platform to identify and engineer novel ligands of target proteins that are implicated in human diseases with unmet medical needs. The lab-based position will be part of our peptide chemistry group. The scientist will work closely with medicinal chemistry and DNA encoded library groups to develop new synthesis and screening technologies on and off beads. The successful candidate will be a skilled experimentalist with deep knowledge of peptide chemistry and synthesis.

Responsibilities:

Synthesize polypeptides with automated peptide synthesizers or manually. Workup, purify and deliver those peptides for biological assays. Design drug-like peptide molecules utilizing medicinal chemistry knowledge, including property-based optimization, and an understanding of ADME, pharmacokinetics and optimal physicochemical properties.
Design and synthesize peptide conjugates with other therapeutic agents.
Develop and implement new methods to advance our peptide drug discovery efforts.
Ensure optimal interaction, communication and provide regular updates on project status to the program leads and leadership team.
Participate in new target identification and validation
Triage screening hits, and carry out hit to lead
Learn to independently lead programs with the goal of delivering of drug candidates

Required Skills:

Proficient in peptide chemistry design, synthesis, purification, characterization, bioconjugation technologies
Deep knowledge and experiences in solid phase peptide synthesis
Experience with chromatography and mass spectrometry data analysis, method development, and applications
Scientist I = PhD with 0 to 2 years of post-doc industry experience or an MS with 6+ years or a BS with 8+ years of industry experience
Scientist II = PhD with 2+ years of post-doc industry experience or an MS or BS with 10+ years of industry experience

Base Comp Range: $99,200 to $130,200

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Market Project and Process Lead (Atlanta, Georgia, US)

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We are looking for a Market Project & Process Lead who is intellectually curious, self-driven, and adaptable to join our Global Supply Chain team based in our Atlanta, Georgia office in the United States. This hybrid position requires a minimum of 40% on site presence and up to 10% domestic/international travel.

About the role
As a member of the US Market Supply Operations (MSO) leadership team, you will provide country-level leadership to US Market Supply Operations (MSO), US Supply Chain, ensuring the organization meets US patient demand through operational excellence, regulatory compliance, and robust governance frameworks. You will set the vision for how MSO operates, embedding audit readiness and stakeholder engagement into every process while driving transformation that accelerates delivery and strengthens adherence to standards. You are accountable for ensuring agility and resilience within a governance-led operating model, positioning the US market as a benchmark for performance, compliance, and innovation.

Who you’ll work with
You will collaborate internally across MSO Leadership, Supply Chain, Quality, Regulatory, Audit/Risk, IT and Digital Technology Teams, Business Continuity, Commercial, and Legal/Privacy. Externally, you will engage with 3PL and distribution partners, regulatory agencies, consultants, technology vendors, and broader industry networks supporting operational, digital, and compliance initiatives.

What you’ll do

Drive operational excellence across US Market Supply Operations by governing processes, standards, and ways of working.
Ensure audit readiness, regulatory compliance, and strong governance across all MSO activities.
Lead strategic projects that improve efficiency, reduce cost to serve, and strengthen supply chain resilience.
Lead digital enablement, including process automation, AI adoption, and enhanced reporting (Power BI, agentive tools).
Manage logistics and supply risks, maintain business continuity plans, and coordinate annual testing and validation.
Coordinate transformation initiatives that improve distribution readiness, including cold chain and network capacity expansion.
Serve as the central governance point for MSO processes, documentation, compliance checkpoints, and continuous improvement.
Run cross functional workshops and governance forums to align teams, resolve issues, and harmonize operations.
Act as a key connector between US MSO and global functions, ensuring alignment with global supply chain standards and strategic priorities.
Monitor performance metrics, identify bottlenecks, and implement corrective actions to improve speed and reliability.
Support U.S. product launches, supply readiness, distribution visibility, and overall market continuity.
Govern vendor performance through structured reviews and integrated performance management.
Coach teams, build capabilities, and promote a culture of continuous improvement, innovation, and accountability.

Interested? For this role we’re looking for the following education, experience and skills
Minimum Education, Qualifications, Skills

Bachelor’s degree in Supply Chain, Operations, Engineering, Business, Information Systems, or a related discipline
10+ years of experience in supply chain, operations, process governance, or transformation roles
Experience operating in regulated environments (pharmaceutical, life sciences, medical, or similarly regulated industries)

Preferred Education, Qualifications, Skills

Proven experience working across market/local and global organizations, aligning local execution with global standards
Demonstrated leadership of cross‑functional, multi‑stakeholder initiatives without direct authority
Master’s degree (MBA or equivalent preferred)
Experience leading or supporting US pharmaceutical supply chain operations
Strong systems and data fluency (e.g., SAP; reporting and analytics tools such as Power BI or Qlik; exposure to EDI / external data sources such as IQVIA)
Global supply chain experience in complex, matrixed environments

This positions reasonably anticipated base salary range is $ 148,000-194,300 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Clinical Account Specialist, Seattle North (Seattle, Washington, US)

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To strengthen our Dermatology Sales Team, we are looking for a talented individual to join our Field Based team in the position of: Dermatology Clinical Account Specialist – Seattle North, Washington.

About the role:

Develop a strong understanding and awareness of the patient journey of care, including taking responsibility for ensuring needed therapies get to the patient.
Offer an outstanding patient experience with our product by communicating clinical information on dermatology products and relevant patient support services to an audience of health care professionals and office staff.
Establish an understanding of the local health care ecosystems, including the payor environment.
Demonstrate the UCB Patient Value Strategy principles by establishing collaborative and team-oriented working relationships and integrating within a matrix environment.
Behave compliantly with all UCB policies / approved messages and coach the team to use of approved UCB sales materials and messages with HCPs and other external stakeholders.

What you’ll do:

Owning responsibility for attaining territory sales goals and objectives through effective territory planning, visiting clinical decision makers with appropriate reach/frequency, collaborating with the Immunology Clinical Specialist and other members of the UCB Patient Value Team.
Analyzing territory data to build and adapt a customer call plan to establish professional working relationships with HCP and support staff.
Maintaining a thorough understanding of the competitive marketplace and drivers of prescriber decisions.
Conducting account related activities such as profiling, call planning, and reviewing UCB sales data with assigned stakeholders.
Making strategic business decisions in the management of allocated resources such as financial/budgets, samples, access opportunities.
Coordinating and supporting promotional educational opportunities and programs intended to expand the knowledge of medical stakeholders and staff (e.g., peer-to-peer educational opportunities) in accordance with UCB policy.

Interested? For this position you’ll need the following education, experience and skills:

Minimum Qualifications:

Bachelor’s Degree BA/BS
Minimum of 3 years of direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry
Must have a valid Driver License with no more than 2 moving violations in the previous three-year period
Must reside within assigned geography

Preferred Qualifications:

5 years of direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry
Experience calling on Dermatologists in the assigned geography
Experience selling injectable biologics products
Proven track record of success in Pharmaceutical Sales demonstrated by goal attainment and awards achievement (President’s Club, etc.)
Biologic product launch experience
Demonstrated business and strategic planning skills to identify unique selling opportunities and adaptability to changing market conditions
Demonstrated understanding of managed care landscape and how it influences/impacts business
Strong verbal, influencing, presentation and written communication skills
Strong collaboration skills and success working in teams

This positions reasonably anticipated base salary range is $132,800-174,300. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Rheumatology Clinical Account Specialist-Queens (New York, New York, US)

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To strengthen our Rheumatology Sales Team, we are looking for a talented individual to fill the position of: Rheumatology Clinical Account Specialist – Queens, NY.

The territory base is Queens but does include southeastern Brooklyn.

About the role

As a Rheumatology Clinical Account Specialist (CAS) you will be responsible for driving demand for the assigned product, by reinforcing the clinical features of the product and UCB value within an assigned territory; engaging and building relationships with clinical decision makers and office support staff to create the best experiences for patients living with severe immunologic diseases who are treated in the home care setting.

Who you’ll work with

Attain sales goals and objectives by product volume as well as other key accountabilities such as reach/frequency with assigned call plan stakeholders
Develops a strong understanding and awareness of the patient journey of care, including the unique needs of patients within the at-home care setting.
Work within the prioritized customer call plan to establish professional working relationships with HCP and support staff.
Offer an outstanding patient experience with our product by communicating clinical information on assigned UCB product and relevant patient support services

What you’ll do

Establishing an understanding of the local ecosystems, including the payor environment, including pharmacy benefits; demonstrating the ability to successfully navigate the complexities of local care delivery systems and models, comprised of multiple payers, with varying degrees of restriction and barriers to patient access for the assigned UCB product.
Maintaining a thorough understanding of the competitive marketplace and drivers of prescriber decisions.
Demonstrating consistent application of the UCB Patient Value Strategy principles by establishing collaborative and team-oriented working relationships, integrating with local UCB ecosystem business partners, in a matrix environment encompassing Field Reimbursement Managers, Immunology Clinical Account Specialist, Partnership Leads, Regional and National Account Executives and Medical Science Liaisons
Knowing when and how to bring in the right expertise at the right time from other UCB matrix roles based on the customer need or opportunity at hand
Conducting account related activities such as profiling, call planning, reviewing UCB sales data, related to at-home administration with assigned stakeholders

Interested? For this role we’re looking for the following
Minimum Qualifications:

Bachelor's degree BA/BS
3 + years direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry
Must have a valid US Driver’s License and with no more than 3 moving violations in the past 2 years
Must reside within assigned territory

Preferred requirements:

Experience selling injectable products
Experience in calling on Rheumatologists
Discussing therapeutic strategies to inform and influence decision makers
Developing and applying clinical and business expertise, and effective selling skills
Executing marketing strategies at the local level
Demonstrated understanding of managed care landscape and how it influences/impacts business

This positions reasonably anticipated base salary range is $132,000-174,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Principal Data Governance Architect (Atlanta, Georgia, US)

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We are looking for a Principal Data Governance Architect to join our Data Governance Team based out of Atlanta, GA (hybrid, 2 days per week onsite)

About the role

The Principal Data Governance Architect advances UCB’s mission by governing U.S. commercial data assets that enable patient insights to drive scientific and business innovation. This role ensures data is Findable, Accessible, Interoperable, and Reusable (FAIR principles)—accelerating digital transformation and supporting informed decision-making. By embedding UCB’s patient value principles and collaborating across functions, the Principal Data Governance Architect strengthens data-driven outcomes and supports UCB’s objectives for scientific excellence, inclusive leadership, and collective success.

Who you’ll work with

The Principal Data Governance Architect partners closely with stakeholders across IT, business units, and the Global Data Office to anticipate organizational needs and translate them into scalable, governed data solutions. Drawing on a deep understanding of enterprise data flows, Systems of Record, and the intersection of business processes with technical architecture, this role guides the strategic evolution of UCB’s data platforms—including Azure Databricks, Collibra, and Power BI—to deliver value for both business users and enterprise data consumers. Reporting to the Head of U.S. Data Governance, the role serves as a connective leader across teams, bridging technical implementation and business intent while strengthening governance accountability, data literacy, and adoption across the organization.

What you’ll do

Data Governance Strategy & Leadership:

Architect and steer the US Data Governance Roadmap for metadata management UCB’s data strategy by proactively identifying critical data gaps, evaluating potential solutions, and aligning cross-functional stakeholders to drive enterprise-wide adoption
Translate business priorities into data architecture roadmaps, oversee execution, and ensure outcomes are communicated in a clear, actionable way to stakeholders at all levels
Drive cross-council and working group alignment, ensuring data governance decisions advance broader enterprise vision and maintain consistency across data domains
Lead data governance decision-making with domain expertise, ensuring appropriate business and technical stewards drive policy, standard, and process development aligned to enterprise objectives
Establish and govern Systems of Record authority across the enterprise, driving alignment on data sharing vision, ownership, and accountability across domains
Define and govern the US Go-to-Market business metadata strategy for Life Science domains (HCP/HCO, Payer, Patient, etc.), ensuring alignment between commercial brand needs and technical schemas

Stakeholder Engagement & Enablement:

Champion data fluency and governance awareness across the organization, enabling business leaders to leverage high-quality, well-governed data for informed decision-making
Serve as the authoritative liaison between IT data teams and business stakeholders, translating technical concepts into business terms and business requirements into technical specifications
Facilitate Data Governance councils and subcommittees, bringing data impact perspectives and proactive insight into scope, vision, and feasibility discussions
Lead and facilitate working groups of business and technical data stewards, driving implementation of policies and processes while fostering capability-building, consistency, and knowledge sharing
Mentor and coach business data stewards in developing their governance expertise, guiding the creation and maintenance of accurate business definitions, business rules, metrics, and metadata
Elevate team capabilities through hands-on technical guidance, knowledge transfer, and establishment of best practices that enable stewards to operate with increasing independence and impact

Platform Alignment & Technical Oversight:

Maintain the Data Intelligence platform (Collibra), ensuring accurate metadata, business glossaries, data dictionaries, and data catalogs are current and accessible
Drive data lineage strategy and implementation across platforms (Unity Catalog on Azure Databricks, Collibra) to ensure end-to-end transparency and traceability of enterprise data flows
Coordinate schedules and managing jobs for ingesting metadata from data sources, ensuring timely synchronization between technical platforms and governance tools
Oversee platform health monitoring and object usage analytics for the Data Intelligence community, driving continuous improvement and optimization recommendations
Partner with IT teams to validate technical implementations against business requirements, providing quality assurance and holding teams accountable for governance deliverables and commitments
Drive strategic collaboration with Digital Technology (IT), Global Data Office, and US Data Operations teams on platform integration requirements and enterprise data policy implementation

Data Quality, Compliance & Reporting:

Ensure appropriate data policies and controls are architected and linked to sensitive datasets (e.g., Financial, PII) with proper implementation across the Data Intelligence community Assist in triage and analysis of data quality issues, supporting impact assessment, mitigation, and remediation activities
Lead impact analysis for data definitions and processes across lines of business, ensuring business continuity, standardization, and strategic alignment with enterprise data architecture
Establish and monitor governance metrics, prepare executive-level reports and strategic recommendations for councils and Steering Committee Drive data maintenance, issue management, and change control excellence for data assets within Data Governance scope, leveraging SharePoint and Teams for collaboration and documentation
Collaborate with business data stewards to create and maintain accurate business definitions, business rules, metrics, and metadata for their respective domains
Lead triage and analysis of complex data quality issues, driving impact assessment, mitigation strategies, and remediation activities with clear accountability and resolution timelines

Interested? For this role we’re looking for the following education, experience and skills

Required:

Master's degree in a quantitative field (e.g., Business, Management Information Systems, Computer Science, Data Science, Information Technology, Analytics, or related field)
10+ years of experience in data management, data governance, or related data stewardship roles
5+ years of experience with data governance platforms and tools (Collibra, Informatica, Alation, or equivalent)

Preferred:

Demonstrated expertise building and scaling Data Catalogs, Data Dictionaries, Business Glossaries, and metadata repositories across multiple business domains
Deep understanding of data flows and the strategic impact of data throughout the system landscape from creation to consumption into downstream business systems and data warehouse/lake environments
Working knowledge of SQL and ability to validate data queries, understand relational data structures, and review technical implementations
Strong understanding of enterprise data architecture principles and industry‑standard design best practices
Knowledge of modern, cloud‑native data pipeline architectures and orchestration frameworks
Proven ability to lead cross-functional initiatives, aligning diverse stakeholders (IT, business, analytics) toward shared governance objectives while ensuring accountability
Track record of mentoring and developing team members, fostering capability-building and knowledge transfer across data governance functions
Collibra certification (Data Steward, Ranger, or equivalent) with demonstrated platform leadership experience
Familiarity with Collibra APIs for technology stack integration and automation
Experience with Unity Catalog on Azure Databricks for data governance and access control architecture
Deep experience with enterprise data lineage tools and automated metadata capture strategies across complex platform ecosystems
Experience with data warehouses (Azure, Snowflake, SQL Server) and reporting/visualization tools (PowerBI)
Experience with data processing, including ETL/ELT workflows and integration patterns from data sources to data warehouses to governance tools
Programming language experience (Python, R) for data analysis and automation
Knowledge of Master Data Management (MDM) and Reference Data Management practices and their roles in enterprise data governance
Familiarity with data privacy and regulatory principles (U.S. federal and state regulations, GDPR, HIPAA, etc.)

This positions reasonably anticipated base salary range is $ 125,600-164,900. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Strategic Meeting Solutions Lead, (Atlanta, GA) (Atlanta, Georgia, US)

Make your mark for patients

Step into a high-impact role where strategic vision meets flawless execution. As our Strategic Meeting Solutions Lead, you’ll shape the future of national and international congresses by driving end-to-end meeting strategy, elevating customer experience, and delivering data-driven results. This is a unique opportunity to influence brand-defining events, collaborate with cross-functional partners, and lead operational excellence across planning, logistics, analytics, and vendor management—all while steering innovation in a dynamic, fast-paced environment.

This position is located in Atlanta, GA or Raleigh, NC.

About the Role

This role leads end-to-end strategy, planning, execution, and continuous improvement of strategic meetings, congresses, and events. The Strategic Meeting Solutions Lead partners cross-functionally to deliver compliant, data-driven, and brand-aligned meetings while overseeing vendors, budgets, analytics, and execution teams.

What you’ll do

Drive strategic vision and innovation for national and international congresses.
Lead end‑to‑end operational strategy and execution for meetings and events.
Align meeting strategy with communication and brand objectives across internal teams and external agencies.
Own the customer experience journey, including analytics, reporting, and effectiveness dashboards.
Prioritize customer experience to achieve congress KPIs.
Oversee planning, logistics, and on‑site execution.
Maintain professional communication and follow up with suppliers, clients, and attendees.
Manage and reconcile budgets, accruals, and financial tracking.
Oversee registration platforms, eRequest workflows, and process optimization.
Ensure compliance with TOV, purchasing standards, and internal policies.
Supervise contractors, including the Meeting Specialist and Coordinator.
Lead vendor evaluations, performance reviews, and quarterly business reviews.
Ensure SOP adherence and support execution teams on compliance.
Maintain and improve internal playbooks and databases.
Oversee logistics vendors and third‑party suppliers.
Support national and local congress planning, including budgeting, room blocks, and execution oversight.

Who you’ll work with

Internal stakeholders to align the meeting and brand strategy.
External agencies supporting planning and execution.
Suppliers, clients, and event attendees for seamless communication.
Contracted team members, including the Meeting Specialist and Coordinator.

Interested? For this role we’re looking for the following education, experience and skills

Minimum Qualifications

Bachelor’s degree or equivalent experience in congress management or related field.
Minimum 5 years Pharmaceutical or regulated-industry meeting experience.

Preferred Qualifications

Proven strategic planning and execution leadership.
Proven operational excellence in congress management.
Digital mindset to advance digital mindset.
Advanced stakeholder and vendor management skills.
Financial acumen, including budget management and accrual tracking.
Process improvement and systems optimization mindset.
Ability to lead analytics and data-driven decision-making.
Excellent communication and presentation skills.
Ability to manage multiple complex programs simultaneously.
Proficiency in Microsoft Office and meeting management platforms.
Ability to travel as required, including occasional weekends.

This positions reasonably anticipated base salary range is $125,600- $164,900 per year. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

External Manufacturing Operations Lead (Devices) (Boston, Massachusetts, US)

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We are looking for a collaborative, dynamic and results driven External Manufacturing Operations Lead (Devices) to join us in our External Manufacturing Operations team, based in any of our HUB locations: Atlanta, GA, Raleigh, NC, Boston, MA. This role can be hybrid (40% on site precence in Atlanta, Raleigh or Boston) or Remote (20% onsite presence) and requires 20% international/ domestic travel.

About the Role
You will lead the operational management of UCB's selected global Contract Development and Manufacturing Organizations (CDMO) & Strategic Vendors. The External Manufacturing Operations Lead is also accountable to manage related projects happening at our Contract Development and Manufacturing Organizations such as technology transfers, new product introductions, and process improvements. In collaboration with Center of Excellence functions, and primarily the Devices, Wearables and Packaging (Device) team, you participate in the development and implementation of the UCB industrial manufacturing.

Who you’ll work with

You will work with internal stakeholders such as External manufacturing business leads, Quality Assurance, Regulatory, Legal, Compliance, Procurement, and Supply Chain. Externally, you will work with contract manufacturing organizations.

What you’ll do:

Oversee day‑to‑day operations with external manufacturing partners, leading regular cross‑functional touchpoints to ensure smooth collaboration, strong communication, and consistent delivery.
Provide technical guidance to strengthen manufacturing performance, drive process efficiency, uphold quality standards, and lead improvement initiatives when issues arise.
Troubleshoot and resolve manufacturing deviations, leading investigations and corrective actions for complex technical or supply challenges.
Coordinate and implement changes with external partners, supporting quality, supply chain, and procurement teams with performance reviews, compliance checks, and continuous improvement efforts.
Plan and manage near‑ and long‑term capacity needs in partnership with Supply Chain to ensure reliable supply and operational readiness.
Lead cross‑functional project teams to execute technology transfers, validation activities, investigations, and business‑support work for both existing and new products.
Support regulatory submission activities, conduct risk assessments with external manufacturers, and follow through on mitigation plans.
Develop business cases and recommendations for external manufacturing decisions and stay current on relevant technologies and market insights to guide strategy.

Interested? For this position you’ll need the following education, experience and skills:

Minimum Experience/Skills Required:

Bachelors Degree
Minimum of 5-7 years of significant operations management experience in a “Good Manufacturing Practice” (GMP) environment

Preferred Experience/Skills:

Master’s degree
International exposure in the pharmaceutical or medical device domain
Strong technical knowledge on device manufacturing
Experience in External Manufacturing functions combined with knowledge in injectables/injection molding and medical devices manufacturing
Knowledge of other languages (French) is an advantage
Ability to lead multi-functional global teams, influence others, hold teams accountable, results orientated, able to manage complex projects from development through commercialization and to attain results
Must be able to manage external business partners and relationships to influence partners to deliver results that UCB needs
Relationship management, including robust communication and networking, internally & externally
Non hierarchical management skills (influencing without authority)
Basic financial & business knowledge
Project Management experience

The reasonably anticipated salary range for this position is $148,000-$194,300 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Account Executive/ New York City Sr. (New York, New York, US)

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To strengthen and support our launches within US Rare Disease Organization (RDO), we are seeking an Account Executive - Neuromuscular (AE) for the New York Sr. territory. The AE is an expert on the practices, delivery networks, and patient populations within their territory.

About the Role

Who you’ll work with

Call plan physicians/HCPs and all care team members
Sales management/leadership
Market Access, Thought Leader Liaison, and Medical Teams
KOLs
Sites of care

What you’ll do

Consistently exceed territory sales objectives while operating with the highest level of ethics and integrity
Create and execute strategic business plans reflecting a thorough understanding of the local market conditions
Master targeted disease states, which include a deep understanding of patient journeys, standards of care, and treatment drivers
Advocate for Rare Disease patients and serve as the authority on the various tools and resources UCB offers to support physicians, pharmacists, and other health care providers
Continuously expand the expertise of all treating and referring physicians, as well as payers, hospital systems, pharmacies, labs, and other components of the care continuum; maintain awareness and remain attentive to the dynamics between different stakeholders that influence patient treatment decisions
Maintain strong relationships within the payer landscape to ensure providers are informed on coverage and reimbursement status; collaborate with the payer access team to ensure all relevant stakeholders are working with the most up-to-date information to maximize access and affordability for patients using UCB products
Foster strong relationships with patient advocacy groups and partners to support appropriate patient education and disease state awareness activities in the community
Collaborate cross-functionally with UCB colleagues to share insights on customer needs and market opportunities; work together towards more effective approaches to patient value creation
Maintain a commitment to continuous improvement (embrace a growth mindset) as evidenced by insights gained/shared about geography, stakeholders, and customer needs through day-to-day experience; growth in core competencies with feedback sought from managers and colleagues, courses taken, on-the-job projects and relevant periodicals/readings

Our 4 Pillars in Rare Disease Organization

Demonstrate great commitment to the Rare Disease patient community and understand the patient journey, the barriers they face in care and treatment, and how to help them overcome those barrier
Utilize innovative methods to identify patients who need treatment
Maintain a highly tactical approach to patient access
Help patients and caregivers navigate the Healthcare System and work around roadblocks

Interested? For this position, you’ll need the following education, experience, and skills:

Minimum Qualifcations:

Bachelor’s Degree
8+ years of field-based experience in sales, account management, and/or field reimbursement in biopharmaceuticals or healthcare, inclusive of 5+ years in a competitive specialty market segment
4+ years of Rare Disease experience in pharmaceuticals/Biologics Field experience with Buy-and-Bill medical benefits, Specialty Pharmacy, and HUB delivery models
Verifiable record of sustained high sales performance and achievement in top 30% nationally
Experience/involvement in successful product launches
The ability to maximize impact of multichannel/digital tools and strategy/tactics with territory HCPs
Command of key medical, scientific, and healthcare concepts, language, and practices related to neurology and rare diseases
Experience serving a variety of call points – academic centers, community-based care, hospitals, and private office practices
Comfortable spending up to 60% of time traveling with overnight travel required (territory business need dependent)

Preferred experience

Significant CNS/neuroscience sales experience (to include epilepsy); Oncology, Hematology and/or Specialty reimbursement products requiring Specialty Pharmacy knowledge and expertise
Experience in supporting biologic therapy administered by a designated health care provider
Promotional product experience with REMS requirements

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Clinical Account Specialist Dermatology - Indianapolis (Indianapolis, Indiana, US)

Make your mark for patients

To strengthen our Dermatology Sales Team, we are looking for a talented individual to join our Field Based team in the position of: Dermatology Clinical Account Specialist – Indianapolis, IN

About the role:

Develop a strong understanding and awareness of the patient journey of care, including taking responsibility for ensuring needed therapies get to the patient.
Offer an outstanding patient experience with our product by communicating clinical information on dermatology products and relevant patient support services to an audience of health care professionals and office staff.
Establish an understanding of the local health care ecosystems, including the payor environment.
Demonstrate the UCB Patient Value Strategy principles by establishing collaborative and team-oriented working relationships and integrating within a matrix environment.
Behave compliantly with all UCB policies / approved messages and coach the team to use of approved UCB sales materials and messages with HCPs and other external stakeholders.

What you’ll do:

Owning responsibility for attaining territory sales goals and objectives through effective territory planning, visiting clinical decision makers with appropriate reach/frequency, collaborating with the Immunology Clinical Specialist and other members of the UCB Patient Value Team.
Analyzing territory data to build and adapt a customer call plan to establish professional working relationships with HCP and support staff.
Maintaining a thorough understanding of the competitive marketplace and drivers of prescriber decisions.
Conducting account related activities such as profiling, call planning, and reviewing UCB sales data with assigned stakeholders.
Making strategic business decisions in the management of allocated resources such as financial/budgets, samples, access opportunities.
Coordinating and supporting promotional educational opportunities and programs intended to expand the knowledge of medical stakeholders and staff (e.g., peer-to-peer educational opportunities) in accordance with UCB policy.

Interested? For this position you’ll need the following education, experience and skills:

Minimum Qualifications:

Bachelor’s Degree BA/BS
Minimum of 3 years of direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry
Must have a valid Driver License with no more than 2 moving violations in the previous three-year period
Must reside within assigned geography

Preferred Qualifications:

5 years of direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry

Experience calling on Dermatologists in the assigned geography
Experience selling injectable biologics products
Proven track record of success in Pharmaceutical Sales demonstrated by goal attainment and awards achievement (President’s Club, etc.)
Biologic product launch experience
Demonstrated business and strategic planning skills to identify unique selling opportunities and adaptability to changing market conditions
Demonstrated understanding of managed care landscape and how it influences/impacts business
Strong verbal, influencing, presentation and written communication skills
Strong collaboration skills and success working in teams

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Rheumatology Clinical Account Specialist-Upstate New York (Rochester, New York, US)

Make your mark for patients

To strengthen our Rheumatology Sales Team, we are looking for a talented individual to fill the position of: Rheumatology Clinical Account Specialist – Upstate New York ( this territory will cover Buffalo, NY to Albany, NY)

About the role

Who you’ll work with

Attain sales goals and objectives by product volume as well as other key accountabilities such as reach/frequency with assigned call plan stakeholders
Develops a strong understanding and awareness of the patient journey of care, including the unique needs of patients within the at-home care setting.
Work within the prioritized customer call plan to establish professional working relationships with HCP and support staff.
Offer an outstanding patient experience with our product by communicating clinical information on assigned UCB product and relevant patient support services

What you’ll do

Establishing an understanding of the local ecosystems, including the payor environment, including pharmacy benefits; demonstrating the ability to successfully navigate the complexities of local care delivery systems and models, comprised of multiple payers, with varying degrees of restriction and barriers to patient access for the assigned UCB product.
Maintaining a thorough understanding of the competitive marketplace and drivers of prescriber decisions.
Demonstrating consistent application of the UCB Patient Value Strategy principles by establishing collaborative and team-oriented working relationships, integrating with local UCB ecosystem business partners, in a matrix environment encompassing Field Reimbursement Managers, Immunology Clinical Account Specialist, Partnership Leads, Regional and National Account Executives and Medical Science Liaisons
Knowing when and how to bring in the right expertise at the right time from other UCB matrix roles based on the customer need or opportunity at hand
Conducting account related activities such as profiling, call planning, reviewing UCB sales data, related to at-home administration with assigned stakeholders

Interested? For this role we’re looking for the following
Minimum Qualifications:

Bachelor's degree BA/BS
3 + years direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry
Must have a valid US Driver’s License and with no more than 3 moving violations in the past 2 years
Must reside within assigned territory

Preferred requirements:

Experience selling injectable products
Experience in calling on Rheumatologists
Discussing therapeutic strategies to inform and influence decision makers
Developing and applying clinical and business expertise, and effective selling skills
Executing marketing strategies at the local level
Demonstrated understanding of managed care landscape and how it influences/impacts business

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Principal Scientist - Translational Muscle Biology (Cambridge, Massachusetts, US)

Make your mark for patients

We are seeking an exceptional Principal Scientist to join UCB's US Neuromuscular group based in Cambridge, MA and contribute to translational biology drug discovery efforts with an emphasis on muscle biology. The candidate will be responsible for leading projects, exploring new biology, designing, characterizing and deploying in vitro or in vivo models and other cellular/biochemical assays to be utilized in early drug discovery for multiple therapeutic programs and target discovery efforts. Collaborate in a matrixed team of scientists responsible for identification and knowledge building across pathobiological pathways and patient populations including those in neuromuscular disease related to nucleotide repeat expansions, genetic mutations, muscle atrophy, mitochondrial/ lysosomal dysfunction or inflammation.

Responsibilities:

Team leadership: Supervise and mentor junior scientists, fostering a collaborative and innovative research environment.
Project management: Oversee multiple projects, ensuring timely delivery of milestones and effective resource allocation.

Innovation: Identify and implement new technologies and methodologies to advance muscle cell biology and translational research.

Model Development: Design, characterize and validate primary cell or stem cell/3D models for therapeutic programs.
Assay Execution: Conduct cell-based functional assays to characterize therapeutic hits or validate new targets that could require gene editing.
Muscle biology: Perform in vivo and in vitro assays to enhance understanding of neuromuscular disease biology.
Team Collaboration: Collaborate with cross-functional teams to integrate translational biology insights into therapeutic programs or new target proposals.
Data Management: Document, analyze, and present data to internal teams.

Requirements:

PhD with 12+ years or MS Degree with 18+ years in drug discovery, biology, cellular biology, bioengineering or related field.

Competencies:

Deep knowledge in muscle biology, and translational assays
Strong assay development and drug discovery knowledge
Strong track record of publishing in high-impact journals and presenting at scientific conferences
Deep experience with mammalian cell culture, molecular and biochemical assays
Strong attention to detail, and enthusiasm for learning
Proven ability to lead projects, supervise and mentor scientists is a plus
Knowledge in mitochondrial biology is a plus

Base Salary Range: $137,600 to $180,600

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Sr. Principal Scientist - Translational Muscle Biology (Cambridge, Massachusetts, US)

Make your mark for patients

We are seeking an exceptional Senior Principal Scientist to join UCB’s US Neuromuscular group based in Cambridge, MA and contribute to translational biology drug discovery efforts with an emphasis on muscle biology. The candidate will be responsible for leading portfolio projects, exploring new biology, and designing in vitro or in vivo models and other cellular/biochemical assays to be utilized in early drug discovery for multiple therapeutic programs and target discovery efforts. Collaborate in a matrixed team of scientists responsible for identification and knowledge building across pathobiological pathways and patient populations including those in neuromuscular disease related to nucleotide repeat expansions, genetic mutations, muscle atrophy, mitochondrial/lysosomal dysfunction or inflammation.

Responsibilities:

Team leadership: Supervise and mentor junior scientists, fostering a collaborative and innovative research environment.

Project management: Oversee multiple projects, ensuring timely delivery of milestones and effective resource allocation.

Innovation: Identify and implement new technologies and methodologies to advance muscle cell biology and translational research.
Model Development: Design, characterize and validate primary cell or stem cell/3D models for therapeutic programs.
Assay Execution: Lead the design of cell-based assays to assess therapeutic candidates or validate new gene-editing targets.
Muscle biology: Drive the design and execution of in vivo and in vitro assays to enhance understanding of neuromuscular disease biology.
Team Collaboration: Collaborate with cross-functional teams to integrate translational biology insights into therapeutic programs or new target proposals.
Data Management: Document, analyze, and present data to internal teams.

Requirements:

PhD with 15+ years or MS Degree with 20+ years in drug discovery, biology, cellular biology, bioengineering or related field.

Competencies:

Proven ability to lead projects, supervise and mentor scientists
Deep knowledge in muscle biology and translational assays.
Strong assay development and drug discovery knowledge.
Strong track record of publishing in high-impact journals and presenting at scientific conferences.
Deep experience with mammalian cell culture, molecular and biochemical assays.
Strong attention to detail, and enthusiasm for learning.
Knowledge in mitochondrial biology is a plus

Base Salary Range: $168,000 to $220,500

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Data Ownership Lead (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Data Ownership Lead with strong patient data expertise who is operationally driven, analytical and passionate to join us in our Global Data Acquisition and Advanced Analytics team. This position can be based in our Atlanta, Georgia, Raleigh, North Carolina, or Boston, Massachusetts.  This hybrid role (at least 40% of the time in office) is limited to 10% travel domestically. 

About the role

You will support the Global Data Acquisition team by onboarding contracted data, ensuring proper data management, and enforcing compliance with regulatory, contractual, and UCB policy requirements. The role requires expertise in global privacy frameworks and provides guidance across the full data lifecycle. You will maintain the Global Data Catalog, supports data users through training and best‑practice communication, and collaborates with Legal, Compliance, IT, the Data Office, and other stakeholders to ensure compliant data usage and manage any remediations needed.

Who you’ll work with

Internally, you will work with the Head of Data Acquisition Strategy, Legal and Compliance Leads (US/Global), IT, Data Office, Purchasing, Finance, Regional Data Operations Teams, Business and Functional Leads/Heads. Externally, you will work with external secondary data vendors, globally.

What you’ll do

You will be responsible for enabling exceptional business impact through expert knowledge and enablement of data assets. As part of this role, you will:

Partner with external data vendors and internal teams to onboard contracted data.
Work with IT, the Data Office, and external partners to ensure data governance aligns with Global Data Office requirements.
Guide data processes across the lifecycle (onboarding, use, retirement/retention) to keep assets current and fit for purpose.
Maintain visibility of all acquired data and keep the Global Data Catalog updated with accurate information and metadata.
Liaise with Global Data Acquisition, IT, Data Office, Legal, and Compliance to meet regulatory, contractual, and policy requirements.
Stay current on privacy and regulatory frameworks (HIPAA, CCPA, GDPR, etc.) and advise teams accordingly.
Ensure compliance of patient‑level data tokenization in the US and globally, including expert‑determination requirements.
Apply risk‑management practices to reduce non‑compliance risks.
Lead remediation efforts with Legal and Compliance when issues arise.
Develop training on data, compliance, and regulatory frameworks for data users.

Interested? For this role we’re looking for the following education, experience, and skills

Required

Bachelor’s degree in quantitative area 
Minimum of 7 years experience working with various forms of pharmaceutical data
Minimum of 4 years of experience partnering with internal and external partners
Minimum of 2 years exposure with quantitative data evaluation

Preferred

Master/Doctor’s degree in quantitative area

Able to thrive in a fast paced, innovative environment while remaining flexible, proactive, resourceful, and efficient

Strong knowledge of the pharmaceutical industry

Deep expertise in healthcare data, particularly U.S. and ex-U.S. patient-level claims data

Strong ability to translate diverse patient data questions into analytical approaches

Creativity in integrating disparate datasets to solve complex business problems

Agile, test-and-learn mindset

Skilled at tailoring communication to both technical and nontechnical audiences

Creative problem-solving mindset to overcome technical and organizational roadblocks

Service oriented and results driven, with strong motivation to deliver meaningful impact

Familiarity with data quality techniques

The reasonably anticipated salary range for this position is $ 148,000-194,300 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global Quality Auditing Lead - REMS & GCP (Raleigh, North Carolina, US)

Make your mark for patients

We are looking for a Global Quality Auditing Lead REMS / GVP & GCP to join our Global Quality Auditing team based out of Raleigh, NC, Atlanta, GA or Boston, MA

About the role

The Global Quality Lead for REMS/GVP & GCP programs will co-create and implement the strategy and delivery of a risk based audit program covering the quality and compliance of the UCB REMS (Risk Evaluation & Mitigation Strategies) and Clinical Trials programs. They are responsible for providing input to processes and areas impacted by REMS, Good Pharmacovigilance Practice (GVP) and Good Clinical Practices (GCP) with respect to the requirements of global and local regulations, guidelines and industry best practice.

Who you’ll work with

This individual will work closely with UCB’s Global Quality Auditing team and inferface directly with representatives from Regulatory Authorities across the world in association with Inspections of the REMS/Pharmacovigilance System and Clinical Practices.

What you’ll do

Lead and/or participate in the development of the risk based REMS & GCP audit program through evaluation of elements of the UCB quality system and their effect on the overall state of compliance of the system.
Plan, conduct, and report on REMS audits of Specialty Pharmacies (SPs), Specialty Distributors (SDs) and program vendors as well as internal system audit to assess compliance with REMS requirements
Perform qualification PV audits of potential new vendors/partners/ Specialty Pharmacies (SPs), Specialty Distributors (SDs) and Coordinating Centres (CC).
Perform GCP audits of potential new vendors/partners for purposes of qualification prior to contractual relationships.
Proactively manage audit findings and CAPAs arising from audits in the Audit Management Tool, using all reasonable efforts to obtain prompt mitigation of deficiencies by responsible functions/persons and escalating concerns as required to senior management.
Manage external auditors and/or vendors as required, ensuring that findings from pharmacovigilance audits are distributed, and responses and CAPAs are tracked and followed up as necessary in the Audit Management Tool.
Support the preparation, hosting and follow up of Regulatory Authority inspections related to REMS/pharmacovigilance and clinical activities at the site inspected, in collaboration with the R&D Quality Management team.
Through active participation to several forums (eg PV Quality Council…) and through direct interaction with colleagues, escalate concerns and provide expert guidance on PV and GCP compliance issues to support the development and implementation of necessary CAPAs and quality improvement measures.
Utilize in-depth knowledge and understanding of current business trends, applicable regulations and quality principles, to collaborate effectively and influence approaches to quality, and ensure work products and output are aligned with regulatory guidelines

Interested? For this role we’re looking for the following education, experience and skills

Bachelors Degree required
3+ years auditing experience in the relevant GVP/REMS-GCP area
10+ years in the pharmaceutical environment
In-depth knowledge and understanding of REMS/Pharmacovigilance and ICH-GCP, applicable regulations (domestic and international), quality principles, relevant business processes and techniques.
Understanding of regulatory requirements for the implementation and maintenance of a REMS compliance program
Practical application of US FDA regulatory requirements
Fluent in written and spoken English. Additional language skills would be an advantage.
Able to travel nationally and internationally as business necessitates, 30% of time on average.

Preferred:

Masters Degree strongly preferred
Certification (Describe): ISO 9001 lead auditor certification as a nice to have, etc.)

This positions reasonably anticipated base salary range is $148,000-$195,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Account Executive / Grand Rapids, MI (Grand Rapids, Michigan, US)

Make your mark for patients

To strengthen and support our launches within US Rare Disease Organization (RDO), we are seeking an Account Executive - Neuromuscular (AE) for the Grand Rapids, Michigan territory. The AE is an expert on the practices, delivery networks, and patient populations within their territory.

About the Role

Who you’ll work with

Call plan physicians/HCPs and all care team members
Sales management/leadership
Market Access, Thought Leader Liaison, and Medical Teams
KOLs
Sites of care

What you’ll do

Consistently exceed territory sales objectives while operating with the highest level of ethics and integrity
Create and execute strategic business plans reflecting a thorough understanding of the local market conditions
Master targeted disease states, which include a deep understanding of patient journeys, standards of care, and treatment drivers
Advocate for Rare Disease patients and serve as the authority on the various tools and resources UCB offers to support physicians, pharmacists, and other health care providers
Continuously expand the expertise of all treating and referring physicians, as well as payers, hospital systems, pharmacies, labs, and other components of the care continuum; maintain awareness and remain attentive to the dynamics between different stakeholders that influence patient treatment decisions
Maintain strong relationships within the payer landscape to ensure providers are informed on coverage and reimbursement status; collaborate with the payer access team to ensure all relevant stakeholders are working with the most up-to-date information to maximize access and affordability for patients using UCB products
Foster strong relationships with patient advocacy groups and partners to support appropriate patient education and disease state awareness activities in the community
Collaborate cross-functionally with UCB colleagues to share insights on customer needs and market opportunities; work together towards more effective approaches to patient value creation
Maintain a commitment to continuous improvement (embrace a growth mindset) as evidenced by insights gained/shared about geography, stakeholders, and customer needs through day-to-day experience; growth in core competencies with feedback sought from managers and colleagues, courses taken, on-the-job projects and relevant periodicals/readings

Our 4 Pillars in Rare Disease Organization

Demonstrate great commitment to the Rare Disease patient community and understand the patient journey, the barriers they face in care and treatment, and how to help them overcome those barriers

Utilize innovative methods to identify patients who need treatment
Maintain a highly tactical approach to patient access
Help patients and caregivers navigate the Healthcare System and work around roadblocks

Interested? For this position, you’ll need the following education, experience, and skills:

Minimum Qualifcations

Bachelor’s Degree
8+ years of field-based experience in sales, account management, and/or field reimbursement in biopharmaceuticals or healthcare, inclusive of 5+ years in a competitive specialty market segment
Field experience with Buy-and-Bill medical benefits, Specialty Pharmacy, and HUB delivery models
Verifiable record of sustained high sales performance and achievement in top 30% nationally
Experience/involvement in successful product launches
The ability to maximize impact of multichannel/digital tools and strategy/tactics with territory HCPs
Command of key medical, scientific, and healthcare concepts, language, and practices related to neurology and rare diseases
Experience serving a variety of call points – academic centers, community-based care, hospitals, and private office practices
Comfortable spending up to 60% of time traveling with overnight travel required (territory business need dependent)

Preferred experience

2+ years in rare/orphan drug experience in a competitive market
Significant CNS/neuroscience sales experience (to include epilepsy); Oncology, Hematology and/or Specialty reimbursement products requiring Specialty Pharmacy knowledge and expertise
Experience in supporting biologic therapy administered by a designated health care provider
Promotional product experience with REMS requirements

This positions reasonably anticipated base salary range is $137,600 - $180,600 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Business Analyst, Global Business Services (Atlanta, Georgia, US)

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We are looking for a Business Analyst to join our Global Business Services team based out of our US headquarters in Smyrna, GA (hybrid, 2 days per week onsite)

About the role
We are seeking a Business Analyst who is passionate about leveraging analytics and automation to transform finance operations. You will play a key role in accelerating finance processes through automated process excellence across the various U.S. GBS functions including:

• Gross-to-Net (G2N)
• Accounts Receivable (AR)
• Accounts Payable (AP)
• Accounting & Reporting (R2R)
• Travel & Expense (T&E)

The ideal candidate will work to ensure strategic alignment with global finance objectives, drive operational excellence, and foster cross-functional collaboration to support business growth and compliance.

Who you’ll work with
Reporting to the Head of Finance, you will actively engage with cross-functional teams throughout the organization, collaborating with both regional and global colleagues within the GBS functions to drive process optimization and deliver efficient, high-quality outcomes. You will be empowered to critically assess and reimagine existing processes by thoroughly analyzing current workflows, collaborating closely with organizational leaders, and proactively proposing innovative, strategic solutions that drive transformation and future readiness.

What you’ll do
• Drive cross-functional collaboration: Partner with the U.S. GBS teams to deliver streamlined, high-quality outcomes that support business growth, process efficiency, and compliance.
• Lead process transformation: Analyze and reimagine existing workflows, proactively identifying opportunities for automation and continuous improvement.
• Strategic partnership: Work closely with organizational leaders to recommend innovative solutions that position the organization for future success.
• Champion operational excellence: Ensure alignment with global finance objectives, driving efficiency, compliance, and best practices across all GBS functions.
• Challenge the status quo: Critically assess established processes and embrace change to foster a culture of innovation.
• Harness advanced analytics: Utilize data analytics and visualization tools (Python, R, SQL, Power BI, Tableau) to generate actionable insights and support decision-making.
• Implement automation solutions: Integrate process excellence technologies such as Robotic Process Automation (RPA), UiPath, and Alteryx to optimize operations.
• Leverage modern data platforms: Employ platforms like Microsoft Fabric, Snowflake, and OneLake to enhance data management and analytics capabilities.
• Apply data science methodologies: Use machine learning, predictive analytics, and modeling tools to drive business insights and transformation.
• Utilize project management best practices: Apply Agile methodologies and process mapping tools (e.g., Visio, Lucidchart) to manage projects efficiently, communication project status, and deliver results.

Interested? For this role we’re looking for the following education, experience and skills
Required:
• Masters degree in Data Science, Business, Finance, Accounting, Computer Science, Engineering or other related field
• 3-5 years in business or comparable work experience
Preferred:
• Demonstrated experience collaborating across teams within a matrixed organization
• Proven ability to engage with management and effectively partner with stakeholders at all organizational levels
• Skilled in identifying performance metrics and developing key performance indicators (KPIs)
• Strong aptitude for explaining processes and envisioning innovative solutions
• Familiarity with finance systems, especially SAP
• Strong analytical mindset and a passion for automation and digital transformation
• Ability to critically evaluate processes, identify gaps, and propose actionable improvements

This positions reasonably anticipated base salary range is $88,000 - $116,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Outcomes Liaison, West (Los Angeles, California, US)

Make your mark for patients

Candidates must reside within the territory and live near a hub airport in the territory.

Up to 75% of travel required, including overnights and some weekends.

About the Role

What You’ll Do

Lead execution of the Epilepsy & Rare Syndromes outcomes and RWE engagement strategy across key accounts.
Build and maintain relationships with C‑suite stakeholders, researchers, and payer decision‑makers.
Identify and develop institutional data opportunities that align with strategic evidence needs.
Support field‑based research collaborations and HEOR data generation.
Serve as an expert communicator delivering clinical and economic value propositions across settings of care.
Partner cross‑functionally to address clinical and HEOR data needs at key accounts.

Who you’ll work with

Senior healthcare leaders, including C‑suite and D‑suite decision‑makers within large medical groups, to support high‑level strategic engagements.
Top‑tier research institutions to advance scientific and outcomes‑focused initiatives.
Pharmacy and medical directors at regional payers, providing clinical and economic insights that inform access and value discussions.
Integrated delivery networks (IDNs) and large medical groups to drive outcomes‑ and RWE‑aligned strategies.
Internal cross‑functional partners—regional business units, marketing, sales, medical affairs, and corporate functions—to ensure coordinated execution across the organization.

Interested? For this role we’re looking for the following education, experience, and skills

Minimum Qualifications

Clinically focused graduate degree (MPH, NP, PA). Doctorate degree (PharmD, MD, DO, PhD, DNP) preferred.
Doctoral candidates: Minimum 8 years industry experience + 3 years HEOR/RWE/Outcomes experience.
Non‑doctoral candidates: Minimum 10 years industry experience + 5 years HEOR/RWE/Outcomes experience.

Preferred Qualifications

Doctorate preferred (PharmD, MD, DO, PhD); non‑doctoral clinicians considered with relevant expertise.
Strong background in external stakeholder engagement and decisionmaker relationship management.
Ability to analyze clinical and HEOR data gaps and deliver meaningful solutions.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Data Evaluation & Enablement Lead (Atlanta, Georgia, US)

Make your mark for patients

We are looking for a Data Evaluation & Enablement Lead with strong patient data expertise who is operationally driven, analytical and passionate to join us in our Global Data Acquisition and Advanced Analytics team. This position can be based in our Atlanta, Georgia, Raleigh, North Carolina, or Boston, Massachusetts.  This hybrid role (at least 40% of the time in office) is limited to 10% travel domestically. 

About the role

You will help strengthen UCB’s data acquisition strategy to meet the evolving data needs of our therapeutic areas and patient populations. You will build fluency across different types of high quality healthcare data, support scalable data platforms and enhance cross-functional efficiency by enabling stronger data usage and insight sharing across the enterprise. You will serve as a strategic partner to patient data users, ensuring data is high quality, well understood, and fit-for-purpose. You’ll also lead profiling, assessment, curation, and analytical exploration of patient-level datasets across the product lifecycle as well as curate and transform data to accelerate insights and improve patient outcomes.

Who you’ll work with

You will also collaborate globally with stakeholders across Data Acquisition, Integrated Insights, Digital Technology/IT, RWE, Advanced Analytics, Medical/HEOR, Translational Medicine, New Product Planning, and Commercial teams—supported by contractors—to ensure data suitability for each use case.

What you’ll do

You will be responsible for driving significant business impact through ensuring we deeply understand the data we acquire, and we use it appropriately for data driven decision making. In this role, you will:

Profile and assess patient-level data for completeness, accuracy, timeliness, and suitability for intended use cases.

Identify gaps and recommend remediation or additional data sources.

Review data for accuracy, consistency, and reliability

Translate stakeholder questions into targeted data mining and exploratory analysis to deliver actionable insights.

Extract and analyze cohorts, patterns, and trends tailored to research, commercial, or operational needs.

Evaluate data fitness for specific use cases and advise on additional requirements helping the data user community to use the right data for their questions.

Apply expertise in real-world data (claims, labs, unstructured data) to support advanced analytics.

Mentor deeper expertise across UCBs patient data community

Foster strong relationships and collaboration with data acquisition colleagues, IT, the Data Office, Compliance and other analytics and business teams to enable the utilization of data assets.
Ideate and partner with digital technology teams to improve analytics interfaces and data usability

Interested? For this role we’re looking for the following education, experience, and skills

Required

Bachelor’s degree in quantitative area

Minimum of 3 years’ experience in analyzing open and closed claims data, EHR, and other patient- level data

Minimum of 5 years’ experience working with various forms of patient level pharmaceutical data

Experience with SQL, R, Python, and other programming languages

Preferred

Master/Doctor’s degree in quantitative area

Able to thrive in a fast paced, innovative environment while remaining flexible, proactive, resourceful, and efficient

Strong knowledge of the pharmaceutical industry

Deep expertise in healthcare data, particularly U.S. and ex-U.S. patient-level claims data

Strong ability to translate diverse patient data questions into analytical approaches

Creativity in integrating disparate datasets to solve complex business problems

Agile, test-and-learn mindset

Skilled at tailoring communication to both technical and nontechnical audiences

Creative problem solving mindset to overcome technical and organizational roadblocks

Service oriented and results driven, with strong motivation to deliver meaningful impact

Familiarity with data quality techniques

The reasonably anticipated salary range for this position is $125,600-$164,900 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Account Executive/ New York City (New York, New York, US)

Make your mark for patients

To strengthen and support our launches within US Rare Disease Organization (RDO), we are seeking an Account Executive - Neuromuscular (AE) for the New York territory. The AE is an expert on the practices, delivery networks, and patient populations within their territory.

About the Role

Who you’ll work with

Call plan physicians/HCPs and all care team members
Sales management/leadership
Market Access, Thought Leader Liaison, and Medical Teams
KOLs
Sites of care

What you’ll do

Consistently exceed territory sales objectives while operating with the highest level of ethics and integrity
Create and execute strategic business plans reflecting a thorough understanding of the local market conditions
Master targeted disease states, which include a deep understanding of patient journeys, standards of care, and treatment drivers
Advocate for Rare Disease patients and serve as the authority on the various tools and resources UCB offers to support physicians, pharmacists, and other health care providers
Continuously expand the expertise of all treating and referring physicians, as well as payers, hospital systems, pharmacies, labs, and other components of the care continuum; maintain awareness and remain attentive to the dynamics between different stakeholders that influence patient treatment decisions
Maintain strong relationships within the payer landscape to ensure providers are informed on coverage and reimbursement status; collaborate with the payer access team to ensure all relevant stakeholders are working with the most up-to-date information to maximize access and affordability for patients using UCB products
Foster strong relationships with patient advocacy groups and partners to support appropriate patient education and disease state awareness activities in the community
Collaborate cross-functionally with UCB colleagues to share insights on customer needs and market opportunities; work together towards more effective approaches to patient value creation
Maintain a commitment to continuous improvement (embrace a growth mindset) as evidenced by insights gained/shared about geography, stakeholders, and customer needs through day-to-day experience; growth in core competencies with feedback sought from managers and colleagues, courses taken, on-the-job projects and relevant periodicals/readings

Our 4 Pillars in Rare Disease Organization

Demonstrate great commitment to the Rare Disease patient community and understand the patient journey, the barriers they face in care and treatment, and how to help them overcome those barriers

Utilize innovative methods to identify patients who need treatment
Maintain a highly tactical approach to patient access
Help patients and caregivers navigate the Healthcare System and work around roadblocks

Interested? For this position, you’ll need the following education, experience, and skills:

Minimum Qualifcations:

Bachelor’s Degree
8+ years of field-based experience in sales, account management, and/or field reimbursement in biopharmaceuticals or healthcare, inclusive of 5+ years in a competitive specialty market segment
Field experience with Buy-and-Bill medical benefits, Specialty Pharmacy, and HUB delivery models
Verifiable record of sustained high sales performance and achievement in top 30% nationally
Experience/involvement in successful product launches
The ability to maximize impact of multichannel/digital tools and strategy/tactics with territory HCPs
Command of key medical, scientific, and healthcare concepts, language, and practices related to neurology and rare diseases
Experience serving a variety of call points – academic centers, community-based care, hospitals, and private office practices
Comfortable spending up to 60% of time traveling with overnight travel required (territory business need dependent)

Preferred experience

2+ years in rare/orphan drug experience in a competitive market
Significant CNS/neuroscience sales experience (to include epilepsy); Oncology, Hematology and/or Specialty reimbursement products requiring Specialty Pharmacy knowledge and expertise
Experience in supporting biologic therapy administered by a designated health care provider
Promotional product experience with REMS requirements

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Digital Lead, Clinical Analytics (Raleigh, North Carolina, US)

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We are looking for a Digital Technology Lead, Clinical Analytics to join our Digital Technology – Clinical Patient Evidence team based out of Raleigh, NC (hybrid)

About the role

This pivotal role centers on leveraging advanced analytics and business intelligence to drive data-informed decision-making across Clinical Operations (GCSO) and digital technology initiatives. The position is responsible for designing and implementing robust analytics strategies that support the full spectrum of clinical trial activities, from planning to execution and optimization.

This role will champion the adoption and integration of cutting-edge analytics and business intelligence technologies—including PowerBI, AI, GenAI, and large language models (LLMs)—to enhance core clinical development processes.

Who you’ll work with

This individual will work in close partnership with stakeholders throughout the clinical development and clinical study operations journey, the role identifies opportunities to harness data, uncovers actionable insights, and translates complex analytics into innovative, scalable business solutions.

What you’ll do

Develop and execute the roadmap for clinical analytics, ensuring alignment with organizational goals, initiatives and industry best practices.
Oversee the planning, implementation, and lifecycle management of clinical analytics projects and platforms.
Ensure successful integration of digital solutions with internal and external systems, including CROs, labs, and regulatory partners.
Assume the role of a system owner (ITSO) for designated projects, ensuring end-to-end responsibility for the success of IT implementations, including computerized system validation activities.
Partner with clinical operations, Clinical Data Management, and various Digital Tech teams to define requirements and deliver scalable, user-centric solutions.
Act as the primary liaison between business stakeholders and technology partners (internal/external).
Demonstrate a broad understanding of internal and external data flows, processes in UCB and Drug Development, and act as a business champion for data as a corporate asset and the digitalization process.
Ensure all digital solutions comply with GxP, GDPR, and other relevant regulatory standards.
Oversee validation, documentation, and audit readiness of clinical analytics platforms.
Drive continuous improvement initiatives, leveraging emerging technologies such as AI, automation, and advanced analytics.
Foster a culture of innovation, encouraging the adoption of new tools and methodologies to enhance clinical trial efficiency.
Manage relationships with technology vendors, ensuring service quality, cost-effectiveness, and alignment with business needs.

Interested? For this role we’re looking for the following education, experience and skills

Required:

Bachelors degree in computer sciences or related field
5+ years of experience in an Information Technology environment required with 3 years of experience in the pharmaceutical industry
Ability to use analytical environments like PowerBI, Spotfire, Qlik to discover insights

Preferred:

Experience with key technology services providers and best practices of the industry.
Experience in business and IT process outsourcing and external partner collaboration.
Experience in system integration
Experience in process assessment, analysis, modelling, improvement and automation methodology.
Experience in system validation in the pharmaceutical industry.
Passion for Data Science and developing analytical solutions
Knowledge in advanced analytics (including machine learning) and data mining technologies

This positions reasonably anticipated base salary range is $125,000 - $165,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Key Account Manager/Manchester (Manchester, New Hampshire, US)

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We are looking for a Key Account Manager (KAM) in Rare Diseases who is patient-focused, exceeds sales objectives, and has worked in a complex selling environment to join us in our Rare Syndromes ∙ Epilepsy US team, based in Manchester, NH.

About the role

You will keep the marketing & sales objectives and key performance indicators at the forefront for customer segments in the assigned territory. Act decisively and responsively by prioritizing budget allocation to meet territory objectives. As well as effectively implementing marketing initiatives to achieve sales goals.

Who you’ll work with?

Effectively collaborate with cross-functional partners (medical, reimbursement support, managed market team, and specialty pharmacy, and others) to communicate customer needs help build and deliver appropriate solutions to meet those needs. Partner with advocacy groups to support patient education and disease state awareness in the local community.

What you’ll do

Exceed sales objectives by implementing marketing initiatives by developing and implementing business plans
Maximize impact by leveraging all available data sets and stakeholder input
Seek qualified leads and effectively profile new accounts, refine call planning/routing to optimize schedules
Working knowledge of the local managed care reimbursement
Emphasizes accountability and the highest standard of ethical conduct.

Interested? For this role, we’re looking for the following education, experience, and skills

Minimum qualifications

Bachelor's degree BA/BS
7+ years of Biotechnology/Biopharmaceutical sales experience
Proven, documented track record of delivering consistent sales results
Experience calling on customers at a variety of call points (i.e., academic centers, community-based hospitals and private practice offices) both in person and virtual

Preferred Qualifications:

2 years of rare/orphan drug experience is highly preferred or significant sales experience in CNS/neuroscience
Promoting products specific to CNS/neuroscience, including epilepsy
New product launch experience
Specialty pharmacy/REMS experience

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Key Account Manager / WI (Milwaukee, Wisconsin, US)

Make your mark for patients

About the role

Who you’ll work with?

What you’ll do

Exceed sales objectives by implementing marketing initiatives by developing and implementing business plans
Maximize impact by leveraging all available data sets and stakeholder input
Seek qualified leads and effectively profile new accounts, refine call planning/routing to optimize schedules
Working knowledge of the local managed care reimbursement
Emphasizes accountability and the highest standard of ethical conduct.

Interested? For this role, we’re looking for the following education, experience, and skills

Minimum qualifications

Bachelor's degree BA/BS
7+ years of Biotechnology/Biopharmaceutical sales experience
Proven, documented track record of delivering consistent sales results
Experience calling on customers at a variety of call points (i.e., academic centers, community-based hospitals and private practice offices) both in person and virtual

Preferred Qualifications:

2 years of rare/orphan drug experience is highly preferred or significant sales experience in CNS/neuroscience
Promoting products specific to CNS/neuroscience, including epilepsy
New product launch experience
Specialty pharmacy/REMS experience

This positions reasonably anticipated base salary range is $144,000- $189,000 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Key Account Manager / Cincinnati (Cincinnati, Ohio, US)

Make your mark for patients

About the role

Who you’ll work with?

What you’ll do

Exceed sales objectives by implementing marketing initiatives by developing and implementing business plans
Maximize impact by leveraging all available data sets and stakeholder input
Seek qualified leads and effectively profile new accounts, refine call planning/routing to optimize schedules
Working knowledge of the local managed care reimbursement
Emphasizes accountability and the highest standard of ethical conduct.

Interested? For this role, we’re looking for the following education, experience, and skills

Minimum qualifications

Bachelor's degree BA/BS
7+ years of Biotechnology/Biopharmaceutical sales experience
Proven, documented track record of delivering consistent sales results
Experience calling on customers at a variety of call points (i.e., academic centers, community-based hospitals and private practice offices) both in person and virtual

Preferred Qualifications:

2 years of rare/orphan drug experience is highly preferred or significant sales experience in CNS/neuroscience
Promoting products specific to CNS/neuroscience, including epilepsy
New product launch experience
Specialty pharmacy/REMS experience

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Benefits Specialist (Atlanta, Georgia, US)

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We are looking for a Benefits Specialist who is detail-oriented, employee-focused, and organized to join us in our Reward & Talent Operations team, based in our Atlanta, Georgia office in the United States.

About the role

You will administer the day-to-day benefit functions for U.S. UCB employees including healthcare, retirement, life, wellness, voluntary, HSA, ESPP, ACA, COBRA and other benefit programs as required. You will be responsible for managing disability, FMLA, and other state leaves. Organizing and facilitating the annual benefit enrollment process and incorporate requested changes in Benefit and Payroll databases. Serve as part of the HR Answers team by responding to both benefit and general HR questions.

Who you’ll work with

You will work as part of a collaborative HR operations team, partnering with payroll, vendors, and internal stakeholders. Together, the team supports employees by providing clear guidance, resolving benefit-related questions, and delivering annual benefit activities such as open enrollment.

What you’ll do

Coordinate new enrollments, terminations and status changes with multiple benefit vendors and systems.
Respond to employee and vendor questions relating to 401(k), Employee Stock Purchase, Medical, Dental, Vision, Short & Long-Term Disability, Leaves and other benefit topics. Document all cases in HR Answers tool as well as answer other HR related questions as part of the HR Answers team.
Manage ESPP program, quarterly purchases, deductions, imports, audits.
Organize and facilitate the annual open enrollment process including communication, system set up, enrolment, audit, etc.
Update and process all benefit deductions in payroll system and manage HSA funding each pay period.
Manage disability and FMLA programs and coordinate benefit payments with payroll.
Manage COBRA processes, including annual enrolment.
Monitor dependent verifications, including domestic partner enrollments.
Ongoing ACA vendor monitoring to maintain compliance. Review and approve forms for required annual reporting.
Follow-up with carriers regarding status of claims for disability plans including responding to calls from managers and employees regarding disability benefits.

Interested? For this role we’re looking for the following

Minimum requirements

Bachelor’s degree or equivalent professional experience
3+ years of experience supporting employee benefit programs
This is a hybrid role (at least 40% of the time in office).

Preferred requirements

Experience supporting U.S. health and retirement benefit plans
Experience with HR systems or payroll systems
Knowledge of leave, disability, or compliance-related benefit processes
Professional benefits certification
Experience working with benefit vendors and payroll partners
Strong attention to detail and ability to manage multiple deadlines
Strong customer service and written communication skills

This positions reasonably anticipated base salary range is $108,000 - $141,800. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Analyst, Government Reimbursement (Atlanta, Georgia, US)

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We are looking for a Government Reimbursement Analyst to join us in our Contracts & Pricing team, based in Atlanta, GA (hyrbid, 2x per week in office)

About the Role

The Government Reimbursement Analyst is responsible for a range of activities related to but not limited to the payment of Government Programs, including State Medicaid, Coverage Gap, TriCare, Manufacturer’s Discount Program and Medicare Inflation Rebates within required timeframes.

Who you’ll work with

Internally, you will work with Accounting and Finance, Government Pricing, Gross 2 Net (G2N) teams, Account Executives as required, SAP team (IT) and collaborate with others as required. Externally, you will work with the State Medicaid Agencies, Model N and other external solution partners.

What you’ll do

Manage contracts and pricing updates & process payments related to assigned Government programs
Manage Medicaid Payment Master for all assigned programs
Process & pay all Medicaid claims and other programs assigned within required time periods\
Serve as the key contact with State Medicaid agencies and must be able to communicate clearly and reconcile discrepancies within required timeframes usually through email
Analyze summarizes and interprets results and makes recommendations regarding the need to dispute any Claim submissions
Responsible for the settlement of programs in both Model N and SAP
Manage or assist with any system testing and upgrades as assigned
Ensure compliance with applicable federal and/or state laws, regulations, and/or agency rules, standards, and guidelines, etc.

Interested? For this role we’re looking for the following

Minimum requirements

Bachelor’s degree in Finance, Accounting, or other analytical-related field
2+ years of relevant experience required

Preferred requirements

Pharmacy Benefit Management (PBMs), pharmacy claims knowledge and/or pharmacy-related experience is preferred
Strong MS Excel working knowledge; SAP & Model N preferred
Ability to levereage data analytics and artificial intelligence (AI) tools to generate insights, support decision-making and improve business outcomes
Power BI and other data analytical software knowledge and experience helpful
Hands-on knowledge of and/or experience with Model N or other Government Pricing software platforms strongly preferred
Working knowledge of government regulations pertaining to Federal and State Medicaid programs preferred
Pharmacy Technician experience preferred
Working knowledge of government regulations pertaining to Federal and State Medicaid programs preferred

This positions reasonably anticipated salary range is $88,000-116,000. The actual salary offered will take into account related knowledge, skills, experience and candidate location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Rheumatology District Sales Leader - Upper Plains (Minneapolis, Minnesota, US)

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We are looking for a Rheumatology District Sales Leader who is motivating, inspiring and leading to join us our Rheumatology organization for the geography of Upper Plains team (Minnesota, Wisconsin, North Dakota, South Dakota, Nebraska and Iowa) based in the Minneapolis, MN area.

About the role

The District Sales Lead Rheumatology role is responsible for driving demand for assigned product(s) by motivating, inspiring and leading Clinical Account Specialists (CAS) activities within an assigned District. The Clinical Account Specialists are charged with engaging and building relationships with Rheumatologists, their allied health professionals, and office support staff

Who you’ll work with

Builds relationships with all internal/external stakeholders, to establish a known, long-term presence of UCB Immunology and establishes an understanding of the local ecosystems, the payor environment, and medical/pharmacy benefits.

What you’ll do

Delivers consistent, compliant sales results of assigned product(s) by leading and directing the activities of Clinical Account Specialists (CAS)
Ensures the execution of company business strategy
Coaches and develops a results-oriented team of CASs who influence medical stakeholders’ use of UCB products
Ensures team understands and applies in-depth clinical and business expertise, along with demonstration of effective selling skills
Maintains a thorough understanding of the competitive marketplace and drivers of prescriber decisions
Ability to drive and/or fly to meetings and client sites. Overnight travel of 25-50% may be required

Interested? For this role we’re looking for the following

Minimum requirements

Bachelor's degree required

3+ years of successful management and/or supervisory experience of a team selling an FDA approved specialty product or device
5 years direct selling experience to healthcare professionals in the pharmaceutical, biotech, device or healthcare industry that has included
Resides within assigned geography
Valid driver’s license required

Preferred requirements

Marketing, Sales Training, Sales Operations or Market Access experience
Completion of a professional leadership development program
Experience in reimbursement
Experience with Injectable/Buy & Bill biologic products
Biologic product launch experience
Experience in calling on Rheumatologists

This positions reasonably anticipated base salary range is $168,000-222,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Scientist I or II / Mass Spectrometry Screening (Cambridge, Massachusetts, US)

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We are seeking a highly motivated and independent Scientist I or II / Mass Spectrometry Screening to join our Discovery Sciences team at the UCB-Boston (Cambridge) site. This role will support early-stage programs across UCB’s therapeutic areas of interest through designing, executing, and interpreting mass spec-based assays for hit discovery and hit to lead optimization. Please note that this is a lab-based position requiring you to be onsite 5 days/week.

Key Responsibilities

Design, develop, and execute Affinity Selection Mass Spectrometry (AS‑MS) assays to support small-molecule and peptide screening in collaboration with discovery teams.
Work as part of a cross‑functional team to develop and deploy mass spec-based screening strategies and communicate results to drive pipeline research programs.
Generate large screening data sets and collaborate with Data Analytics team to leverage data for hit selection and SAR generation.
Maintain, troubleshoot, and improve MS instruments and workflows.
Stay current with advances in mass-spectrometry based technologies and emerging methodologies in the field.

Required Qualifications

MS or PhD in Analytical Chemistry, Chemistry, Biochemistry, or related discipline. Recent PhD graduates with strong hands-on AS‑MS experience are encouraged to apply
Demonstrated expertise in mass spectrometry. Direct experience with AS/MS, MS/MS, and library screening is preferred.
Prior knowledge of the relevant application area (e.g., discovery screening, protein–ligand interactions, small-molecule analysis)
Strong analytical thinking, problem‑solving, and scientific communication skills

Preferred Qualifications

Experience with developing and prosecuting peptide-based library screening using MS is highly preferred.
Experience with LC–MS, HRMS, and MS/MS in the context of AS‑MS workflows
Experience working in a discovery or industry research environment is a plus
Publications or conference presentations in mass spectrometry or related fields.

Salary:

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Clinical Development Lead - Raleigh (Raleigh, North Carolina, US)

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About the role

Who you’ll work with

What you’ll do

Set the global clinical development strategy for assigned asset(s), ensuring alignment with TPVP, regulatory requirements, and commercial goals.
Lead external engagement with global thought leaders, investigators, and stakeholders to continuously refine strategy based on emerging insights and unmet needs.
Design and adapt robust clinical development plans that integrate the latest scientific, regulatory, operational, and payer perspectives—balancing innovation with executional feasibility.
Oversee the execution of pivotal studies and regulatory submissions across all relevant markets, ensuring clinical excellence, data integrity, and timely delivery.
Shape clinical narratives and regulatory strategy, acting as a key representative in interactions with global health authorities and strategic partners.
Contribute to corporate strategy, supporting business development initiatives and representing the clinical perspective in asset evaluations.

Interested? For this position you’ll need the following education, experience and skills:

Basic Requirement:

Advanced degree (MD, PhD, PharmD, or equivalent).

Preferred Requirements:

Track record of leading complex global programs across multiple indications.
Familiarity with digital health technologies, real-world data, and AI-enabled trial innovation.
Ability to lead through ambiguity, make informed decisions in uncertainty, and drive results across organizational boundaries.
Strategic mindset with a bias for innovation, speed, and operational excellence.
Exceptional communication and stakeholder management skills, including C-suite level.
Global experience and cultural fluency; willingness to travel internationally as needed.

#TeamUCB

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

ucbCARES Engagement Science Partner (Atlanta, Georgia, US)

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We are looking for an Engagement Science Partner who is empathetic, clinically knowledgeable, and service‑driven to join our UCBCares team, based out of our US Headquarters outside of Atlanta, GA.

About the role

You will serve as a trusted clinical resource providing education and support to patients, caregivers, and healthcare professionals. You will triage and respond to inquiries related to product information, access, adverse events, and general patient support while delivering an exceptional customer experience.

Who you’ll work with

You will collaborate closely with cross‑functional internal partners, including medical, safety, access, and customer experience teams. You’ll also interact directly with patients, caregivers, and providers as a frontline representative of UCBCares.

What you’ll do

Provide education and support to patients, caregivers, and healthcare professionals on products, resources, and services.
Respond to inbound inquiries with empathy, professionalism, and customer‑first focus.
Identify and resolve barriers related to product access, insurance, reimbursement, and general support.
Accurately document all interactions in CRM systems and escalate appropriately.
Ensure timely follow‑up and resolution of inquiries while maintaining compliance (HIPAA, FDA, SOPs).
Share insights with UCBCares leadership and maintain up‑to‑date product knowledge.

Interested? For this role we’re looking for the following minimum requirements:

Minimum requirements

Active Registered Nurse (RN) license.
Minimum 3 years of clinical experience with patient education or support responsibilities.
Experience in patient‑facing or customer service roles.
Strong interpersonal and communication skills.
Experience using CRM systems.

Preferred qualifications

BSN degree.
Ability to translate complex clinical information into patient‑friendly language.
Strong problem‑solving and conflict‑resolution skills.
Demonstrated empathy, patience, and customer‑first mindset.
Ability to work independently and collaboratively within multidisciplinary teams.
Skilled in prioritizing and multitasking in a fast‑paced environment.

This position’s reasonably anticipated base salary range is $108,000 To $141,800 per year. The actual salary offered will consider internal equity and may also vary depending on the candidate’s region, job-related knowledge, skills and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

E&BI Monitoring Program Lead US (Atlanta, Georgia, US)

Make your mark for patients

Make your mark for patients
We are looking for an E&BI Insights Monitoring Program Lead who is an experienced, strategic, analytical, and collaborative healthcare compliance professional to join us in our compliance function team, based in our UCB office in Atlanta, GA.

About The Role

As the Ethics & Business Integrity (E&BI) Insights Monitoring Program Lead, you will be part of the broader healthcare compliance team. In this role, you will shape the strategic direction, execution, and continuous enhancement of UCB’s monitoring programme. You will oversee the design and successful implementation of monitoring plans, manage monitoring vendors, and introduce innovative ways of working, while collaborating closely with the wider E&BI team to deliver clear and comprehensive communication to local stakeholders. Based in the United States, this role offers the opportunity to take ownership of key operations and work seamlessly with global teams. If you are passionate about healthcare compliance and eager to drive meaningful impact, apply now to join a forward‑thinking, globally connected organization.

Who You’ll Work With
You’ll collaborate closely with the US E&BI Leads, business units, and cross-functional teams. You’ll also act as a key liaison between regional teams and global monitoring leadership, facilitating best practice sharing and continuous improvement initiatives.

What You’ll Do

Develop and refine monitoring strategies and annual plans in line with business needs
Collaborate with regional leads to align monitoring with local regulations
Oversee and manage external vendors for E&BI monitoring activities
Report monitoring activities, findings, and trends to senior leadership
Manage High Impact Findings (HIF) and drive continuous improvement
Use analytics tools to provide actionable insights

Minimum Requirements

Bachelor’s degree or higher in a relevant field
5+ years’ experience in US healthcare compliance or risk management

Preferred Requirements

At least 2 years in a leadership or managerial role
Experience leading teams or managing vendors in a multinational environment
Proven expertise in global healthcare regulatory standards and compliance analytics
Relevant professional certifications (e.g., CCEP, CFE, CPA, CHC, CCEP-I)
Experience with advanced analytics tools (e.g., Qlik, Power BI)
Strong project management and communication skills
Experience presenting to senior leadership and external stakeholders
Ability to adapt monitoring plans to diverse regulatory environments

This positions reasonably anticipated base salary range is $124,000 to $162,800 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Medical Science Liaison Dermatology - Nashville (Nashville, Tennesee, US)

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About the role

Who you will work with:

This position will support our Immunology Patient Value Unit (PVU) in an assigned geography of South Ohio, Kentucky, and Tennessee.

What you’ll do:

Maintain deep scientific knowledge in areas of Dermatology while delivering clinical value propositions and engages with key decision-maker stakeholders in medical groups, IDNs, and regional payers
Identifies and supports potential research expansion projects/collaborations, medical advisors, and educational partnership opportunities
Conducts local roundtables and education programs that aim enhance Key Opinion Leaders (KOL)s understanding of unmet clinical needs
Serve as a scientific expert at key medical and scientific conferences, advisory boards, clinical investigator meetings, and internal meetings.
Supports field-based cross-functional teams to provide medical expertise in access engagements as needed as well as provide field updates regarding topics of interest for creation and/or updating of Standard Response Letters
Reviews and critiques scientific publications to help inform healthcare trends in Dermatology
Collects, analyzes, and communicates information concerning therapeutic area, treatment options, emerging standards of care, and competitive intelligence as well as addresses medical information inquiries
Provides effective clinical presentations to internal and external audiences and tailors presentations to meet specific audience needs through peer to peer scientific exchange
Assesses feasibility and serves as the primary liaison between UCB and investigator for unsolicited Investigator-Initiated Studies (IISs) from inception to publication

Interested? For this role we’re looking for the following education, experience and skills

Minimum Requirements:

Doctorate degree (PharmD, MD, DO or PhD in a relevant field) required.
Valid US Driver’s License and with no more than 3 moving violations in the past 2 years
Must reside within the assigned territory
Must complete initial training and successfully pass all assessments within 90 days of hire

Frequent business travel required, including overnights and some weekends.

Preferred Requirements:

3+ years of field medical experience preferred.
Immuno-dermatology experience strongly preferred. Prior product launch experience also preferred.
Basic business acumen with a solid understanding of the pharmaceutical industry
Basic knowledge and understanding of health economic principles and clinical trials
Ability to clearly articulate complex scientific concepts in 1:1 and group settings
Strong interpersonal skills and excellent verbal and written communication skills
Creative approach to problems solving and able to work effectively in a constantly changing environment
Must be a strong team player and effectively interface with other internal departments including regional business units, marketing, sales, medical affairs, and clinical operations
Strong time management, and organizational skills with proficiency in Microsoft applications

This positions reasonably anticipated base salary range is $156,000-204,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Neurology Specialty Sales Representative, Pittsburgh, PA (Pittsburgh, Pennsylvania, US)

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We seek a Neurology Specialty Sales Representative who will take ownership of a dynamic Pittsburgh territory, bringing UCB’s Epilepsy and Acute Care portfolio to life while driving strong business results and real patient impact. This territory includes the major cities of Erie, Altoona, Dubois, Pittsburgh, Morgantown (WV), Huntington (WV), and Charleston (WV). Candidates should reside in the territory.

About the role

As a Neurology Specialty Sales Representative, you’ll be on the front lines, building influential relationships with healthcare professionals, hospital systems, long-term care facilities, advocacy organizations, and payer partners to expand access and accelerate adoption. You will partner cross-functionally, deliver value-based solutions to physicians and clinics, and serve as a passionate, informed advocate for patients living with epileptic diseases, helping ensure the right therapies reach the right patients at the right time.

What You’ll do

Own and grow a defined territory by serving as the primary point of contact for targeted healthcare providers (HCPs) and office staff.
Drive prescription demand and market share by effectively positioning UCB’s therapeutic solutions with the right patients at the right time.
Execute a territory business plan aligned to national and regional sales objectives to deliver consistent results.
Identify, prioritize, and engage high-value accounts at optimal frequency to influence prescribing behavior and accelerate adoption.
Deliver persuasive, compliant sales presentations using approved messaging and tools to advance customers along the adoption continuum.
Leverage data, insights, and analytics to target accounts, optimize call planning, and maximize territory performance.
Build and maintain strong relationships with key local, regional, and national thought leaders to expand UCB’s footprint.
Manage territory resources, including meeting and speaker program budgets, to achieve objectives on time and within budget.
Participate in key meetings, congresses, and customer events; travel regularly within the territory, with up to 50% overnight travel as required.

Who you’ll work with

Conduct sales calls with physicians and care providers throughout the territory to provide appropriate and compliant solutions for patient needs.
Collaborate with your UCB teammates to maximize UCB’s impact within the region.
Build relationships with key influencers in epilepsy and serve as UCB’s primary point of contact with these stakeholders.

Interested? For this position you’ll need the following education, experience and skills:

Minimum Qualifications:

Bachelor’s degree
Minimum of 5 years’ experience calling on customers at a variety of call points (e.g., academic centers, community-based, hospitals, and private practice offices), both in person and virtual, unless the market necessitates otherwise.
Valid U.S. Driver's license with no more than two moving violations in the last three years

Preferred Qualifications:

Promoting products specific to CNS/neuroscience, including epilepsy
Proven, documented track record of delivering consistent sales results
New product launch experience

This position's reasonably anticipated salary range is $94,400 to $157,500 annually. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Alternative Market Access Strategy Lead (Raleigh, North Carolina, US)

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We are looking for an Alternative Market Access Strategy Lead to join our Market Access & Pricing Business Unit based out of either Atlanta, GA or Raleigh, NC

About the role
At UCB, we believe every patient deserves timely, affordable, and seamless access to the therapies that change lives. The Market Access Strategy Lead, DTP (Direct to Patient) will report to the Alternative Access Strategy Lead and will help redefine how care reaches people by turning barriers into bridges. DTP is an essential complement to UCB’s longstanding commitment to patient-centric access and to broader industry progress, meeting rising expectations for convenience, transparency, and choice. In this role, you will shape our vision for a future where medicines are easier to reach, powered by innovative partnerships and modern digital platforms that extend care beyond traditional channels. Your leadership will put patients first by accelerating access, removing friction, and improving time to therapy, affordability, and adherence so more people can live their best lives.

What you’ll do

Define the long-term vision and roadmap for DTP across UCB’s U.S. portfolio, ensuring alignment with patient centric access principles and corporate objectives.
Build compelling business cases for investment in DTP initiatives, including pilots and scaleup strategies.
Lead cross-functional integration for patient impact
Drive collaboration with Market Access, Trade, Policy, Legal, Compliance, Finance, IT/Digital, and Business Units to embed DTP into launch and lifecycle planning.
Ensure seamless alignment between affordability solutions, reimbursement pathways, and patient support programs.
Design and optimize patient-first models
Develop innovative DTP program designs that prioritize speed to therapy, affordability, and adherence while balancing risk/benefit to UCB.
Serve as UCB’s subject matter expert on DTP partners and models.
Use analytics to inform pricing constructs, channel strategies, and forecasting; anticipate DTP impact on gross to net and overall brand performance.
Establish KPIs focused on patient outcomes and experience; monitor performance and recommend optimizations based on insights and ROI.
Integrate DTP considerations into launch strategies for new products; lead test and learn pilots and scale successful models across brands.
Partner with marketing and patient engagement teams to ensure messaging reflects the value of DTP for patients and caregivers
Align strategy with legal, compliance, and regulatory requirement
Champion innovation and continuous improvement

Interested? For this role we’re looking for the following education, experience and skills
Required:

Bachelor’s degree in Business, Health Policy, Pharmacy, Data/Analytics, or related field (MBA/MPH a plus).
10+ years of biopharma experience, with significant expertise in Market Access, Trade/Supply Chain, Channel Strategy, Patient
Support/HUB, Specialty Pharmacy, Digital Health, or adjacent access and fulfillment domains.

Preferred:

Demonstrated ability to design or navigate patient access solutions that improve affordability, time to therapy, and adherence within U.S. healthcare channels.
Strong analytical skills with fluency in forecasting, pricing constructs, gross-to-net drivers, and performance dashboards.
Working knowledge of U.S. regulatory and compliance considerations relevant to patient access and distribution (for example, pharmacy and telehealth rules, price reporting sensitivities, privacy).
Proven ability to manage and influence a broad range of stakeholders across multiple functions and levels, driving alignment and execution on complex initiatives.
Excellent communication, influence, and storytelling skills with a track record of aligning cross-functional teams around clear, patient-first decisions.

This positions reasonably anticipated base salary range is $ $164,000 - $216,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technical Lead, Patient Support Solutions (Atlanta, Georgia, US)

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We are looking for a Technical Lead, Patient Support Solutions to join our Digital Technology team based out of Atlanta, GA (hybrid, 40% onsite)

About the role

The Technical Lead, Patient Support Solutions partners with the UCB business unit teams to lead projects, use technology systems, and manage technical support resources (internal and/or external) to support patient support/experience programs.

Who you’ll work with

This role will work closely with internal stakeholders (Patient Support Program, Data & Reporting, Marketing etc.) as well as external vendors & partners.

What you’ll do

Possesses the ability to analyze, manage, implement, train end-users, and support technical systems and associated business processes.
Assists with technology specifications and implementation plans.
Provides technical and business analyst expertise involving the design, development, construction and on-going support of systems, processes, integrations, or methods.
Provide technical support in the deployment of purchased application as well as overseeing system design, development, implementation, and maintenance of internally developed applications. Involved in defining, managing, and supporting interfaces between multiple vendors and systems.
Provides strategic business analyst expertise of systems, processes, or methods.
Responsible for delivering attainment of project plans, milestones, deliverables, and financial targets for assigned projects and programs.
Engage with key stakeholders to develop trusted relationships
Serve as the IT SME for U.S. Patient Support Programs. Maintain awareness of industry trends, identify opportunities for business process and technology improvements and value creation.
Support the evaluation, selection, and management of vendors and partners.

Interested? For this role we’re looking for the following education, experience and skills

Required:

Bachelors Degree
7+ years’ experience in full systems life cycle management and deployment experience
4+ years of experience in the pharmaceutical or healthcare industry related to Patient Support/Experience Programs (Data aggregators, co-pay and reimbursement partners, specialty pharmacies and third-party data sources, etc.)

Preferred:

Experience in the support of computerized System Validation, part 11 compliance
Experience with technology systems to support commercial/go-to-market teams in the life sciences industry
Strong understanding of HIPAA requirements (Data Security, Encryption, storage, handling, etc) and associated system impacts.
Thorough understanding of project management methodology and system development lifecycle principles, validation & qualification

This positions reasonably anticipated base salary range is $124,000-163,000. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Manager, Go-to-Market Data Science (Atlanta, Georgia, US)

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To strengthen our Global Advanced Analytics team, we are looking for an adaptable, collaborative individual with an intrapreneurial mindset for our Senior Manager, Go-to-Market Data Science opening. The Go-to-Market domain encompasses the commercial, medical, and market access facets of the business. This hybrid role is based in our Atlanta, GA, Raleigh, NC or Boston, MA offices, requiring 40% onsite presence.

About the role
You will be responsible for making exceptional business impact with the use of secondary data and insights development through advanced analytics methods, enabling an increased use of data and, where applicable, reducing the necessity for building primary data. You will also be responsible for managing and implementing advanced analytics/AI projects to ensure successful delivery. You will oversee the ongoing operations of advanced analytics solutions to ensure that models continue to work and scale them up with additional demand and applications. You will serve as the subject matter expert for Advanced Analytics/AI capabilities in support of business needs.

Who you’ll work with
You will work with the Global Advanced Analytics Team Leads, US and Global Go-to-Market Teams, Integrated Insights Hub Leads, as well as business stakeholders in the Patient Value Units. Externally, you will work with payors and analytics vendors that support data science projects. The mission of this role is to deliver data-driven actionable insights from advanced analytics that create high impact patient value.

What you’ll do

Analytics Leadership: Provide clear expertise for opportunities to leverage advanced analytics, especially where they are advantageous to reducing the need for primary data or have high marginal impact
Deliver the most impactful data and analytics projects that:

address the most compelling business questions, and/or
identify new opportunities for patients and UCB through effective visual displays of quantitative and qualitative information

Partnership and Collaboration: Be the key strategic partner for the Go-to-Market or functional stakeholders and co-create plans and priorities for data and advanced analytics with them together with the Go-To-Market Hub Leads. Ensure tight relationships and collaboration with IT, Data Office, and other Analytics teams using relevant data sources
Team Leadership. Serve as a mentor and guide to more junior data scientists and translators in demonstrating the application of cutting-edge analytics, clear communication and presentation of insights and practical/pragmatic implementation of key recommendations
Drive the execution of regional and local data-driven insights research and data analytics plans and priorities
Foster a strong data science community with significant business acumen and communication skills across Hubs and EngineSupervise the conduct of advanced analytics studies in a collaborative manner ensuring that the study methodology is appropriate to deliver reliable results.
Improve the team’s partnership with, and impact on, key internal (UCB) and external stakeholders within the specific area of focus by:

developing and executing a communication and collaboration plan with key UCB stakeholders
increasing personal and the Advanced Analytics team’s knowledge of the business by ensuring that she/he and each team member has direct interaction with patients and/or other external stakeholders

Attract, retain, motivate, and develop key talent for the Advanced Analytics team; coach and develop team members
Drive deep partnership with the Hub insights team and other “fellow” Engines and insights generating functions (e.g. regional analytics teams) allowing for a joined delivery of cross-functional, deep impactful insights
Be a champion for a data-driven, decision-making culture

Interested? For this role we’re looking for the following education, experience and skills

Minimum Experience/Skills Required:

Bachelor's degree in quantitative area
Minimum of 6-8+ years experience applying predictive modeling techniques such as ML, decision trees, ensemble learning, neural networks etc, and data transformation such as data cleansing and integration, fuzzy matching, etc.
Minimum of 6-8+ years of experience developing program/project plans and leading programs/projects from initiation to implementation
Minimum of 6-8+ years of experience with programming and application development using Python or R

Preferred Experience/Skills:

Master/Doctor’s degree in quantitative area
Knowledge of pharmaceutical industry, ideally specialty pharma and biologic treatments
Deep expertise in leveraging data science methodologies within the Go-to-Market sphere of the pharmaceutical industry. The Go-to-Market domain encompasses the commercial, medical, and market access facets of the business
Expertise in analyzing a range of large, secondary transactional databases, unstructured data or other computationally difficult challenges
Mastery of project management skills
You are a structured problem solver
Possess an 80/20 mindset to push for fast model iterations
Ability to interpret model results and identify potential model errors (e.g., overfitting, model bias, correlation vs causation)
Global role, so willingness and flexibility to work across geographies / time zones (sometimes outside of core hours)

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

US Investment & Infrast Category Lead (Atlanta, Georgia, US)

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We are looking for a Regional Category Lead for the US Manufacturing development program who is strategic, collaborative, and results-driven to join us in our Procurement team, based in our Atlanta, GA office

About the role

As a Regional Category Lead, you will own all procurement activities for the US Manufacturing development program, ensuring alignment with global strategies and compliance frameworks. You will manage end-to-end external spend across engineering, construction, equipment, and services for a new US manufacturing facility, driving sourcing strategies, contract execution, and supplier performance while embedding sustainability and risk mitigation objectives.

Who you’ll work with

You will report to the Head of Procurement Engineering & Infrastructure and partner closely with executive leaders in Operations, Global Engineering, Global Quality, Finance, Legal, and Sustainability. You will also lead and develop a team of category managers, acting as a senior business partner and regional focal point for procurement excellence.

What you’ll do

Develop and implement procurement strategies for US footprint development.
Lead sourcing, contract negotiations, and supplier performance management.
Drive value creation, cost savings, and supply resilience initiatives.
Ensure compliance with ethical, legal, and sustainability standards.
Manage procurement budgets and resource planning for US scope.
Align US sourcing strategies with global category roadmaps.

Interested? For this role we’re looking for the following

Minimum requirements

Master’s degree or higher.
More than 10 years’ experience in similar procurement roles.
Proven leadership experience managing high-performing teams.
Strong negotiation skills and commercial acumen.
Deep understanding of global supply markets and emerging technologies.
Fluent in English with excellent written and verbal communication skills.

Preferred requirements

Professional certifications such as CIPS, CPM, or PMP.
Experience in procurement for large-scale engineering or construction projects.
Proficiency in SAP Source-to-Contract and procurement processes.
Demonstrated commitment to sustainable sourcing and ethical practices.
Strong project management and analytical skills.

This positions reasonably anticipated base salary range is $184,000 to $241,500 per year. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Chef d'équipe Filling (Braine L'alleud, Walloon Brabant, BE)

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Nous recherchons un·e chef.fe d’équipe Formulation – Injectables (F/H/X), qui est pragmatique, orienté·e sécurité & qualité et coach dans l’âme, pour rejoindre notre Département Injectables – Formulation, basé sur notre campus UCB de Braine‑l’Alleud, Wallonie, Belgique.

À propos du rôle

Vous allez piloter au quotidien les opérations de formulation d’injectables et garantir la livraison des objectifs à court terme. Vous allez ancrer une culture sécurité, amélioration continue et “green”, gérer le planning de l’équipe de formulation, coacher les opérateur·rice·s et traiter en première ligne les déviations. Vous allez maintenir une conformité qualité exemplaire, optimiser les stocks et agir comme backup entre chefs d’équipe et Team Leader Remplissage. Votre leadership de proximité fera progresser les personnes, la performance et la fiabilité de la zone.

Avec qui vous allez travailler

Vous allez collaborer au quotidien avec le Team Leader Remplissage, les chefs d’équipe de la zone injectables, les équipes Qualité, Support et HSE, ainsi qu’avec la Planification, la Maintenance et l’Approvisionnement. Vous allez évoluer dans un environnement de production collaboratif, où les rituels d’animation à intervalle court, le feedback continu et l’entraide favorisent la résolution rapide des problèmes et la montée en compétences de chacun·e.

Ce que vous allez faire

Vous allez déployer une culture sécurité, amélioration continue et “green” dans la zone Formulation.
Vous allez planifier, ajuster et suivre le planning journalier des activités de formulation.
Vous serez responsable du coaching, de la formation et de l’engagement des opérateur·rice·s.
Vous allez gérer en première ligne les déviations et anomalies détectées sur le terrain.
Vous allez garantir la conformité aux systèmes de qualité et l’excellence 5S de la zone.
Vous serez impliqué dans les revues documentaires dans Source (Veeva) et collaborerez avec les équipes support pour la mise à jour documentaire.
Vous allez piloter les stocks produits, matériels et consommables, et la revue des dossiers de lot.
Vous serez amené à être le backup entre chefs d’équipe durant les congés ou absences

Intéressé·e ?

Pour ce rôle, nous recherchons les études, expériences et compétences suivantes

Diplôme CESS
5+ ans d’expérience en production ; la formulation d’injectables est un atout.
Expérience confirmée en management d’équipe et développement des compétences.
Capacité à décider avec sang‑froid, sens des priorités et communication constructive.
Maîtrise des exigences qualité et des bonnes pratiques de fabrication.
Maîtrise des outils bureautiques (Suite Office : Word, Excel, Outlook, Teams)
Pratique de l’amélioration continue (5S, housekeeping, résolution de problèmes).

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Pharmacometrics Lead AI/Machine Learning - UK, Belgium or Germany (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Pharmacometrics Lead AI/Machine Learning who is innovative and agile to work in our Quantitative Clinical Pharmacology group, based in our research site in Slough (UK), Monheim (Germany) or Braine (Belgium).

About the role

Developing, implementing and leading Pharmacometrics AI/ML strategy to support development of our assets. Extrapolation (where appropriate), dose selection, trial design, PIP development and ongoing evaluation of data as generated.

Who you’ll work with

Reporting to Global Head of Pharmacometrics.

What you’ll do

Evaluating and implementing emerging technologies for quantitative clinical pharmacology and pharmacometrics applications.
Performing hands-on AI/ML, population PK/PD, exposure-response modeling and clinical trial simulations on an assigned project.
Developing submission ready fit for purpose Pharmacometrics analysis plans and reports.
Initiating and overseeing outsourced pharmacometrics and AI/ML activities and further internalizing the work as needed.
Supporting the development of a team from both a technical and scientific perspective to ensure state of the art pharmacometrics approaches are applied to optimize drug discovery and development.
Having a working knowledge about the regulatory pathways on a global basis and opportunities for collaboration with health authorities (either through working parties, advice meetings, and other initiatives) in Paediatrics, Neurology and Immunology.
Working closely with the QCP Leads assigned to the various projects to ensure clear integration of the pharmacometrics aspects into the programs.
Promoting MID3 internally and externally.

Interested? For this role you'll need the following education, experience and skills

Doctorate (PhD or MD) in the related disciplines of pharmaceutical sciences, statistics or engineering.
8+ years (Bio)pharmaceutical industry experience in pharmacometrics with at least 2 years of experience in the applications of AI/ML in drug development.
Hands-on experience in population PK/PD, disease progression modeling, and clinical trial simulations.
Strong understanding and knowledge of Bayesian methodologies, and model-based meta-analyses.
Hands on Expertise in R, Python, Matlab, NONMEM or related pharmacometrics software.
Agile mindset with a proven ability to adjust by prioritizing multiple tasks.
Outstanding communication, organizational and presentation skills.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Engineering Safety Lead (Braine L'alleud, Walloon Brabant, BE)

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We are looking for an Engineering Safety Lead who is passionate about safety culture, skilled in influencing positive behaviors, and committed to continuous improvement to join our Global Engineering team, based at our UCB campus located in Braine-l'Alleud, Belgium.

About the role:
You will play a pivotal role in shaping and embedding a strong safety culture across our global engineering organization. You are going to inspire safe behaviors, empower teams to take ownership of safety, and integrate safety thinking into every stage of engineering project delivery.

This role is pivotal in leading a shift from compliance-driven safety to a deeply embedded, values-based safety culture within global engineering projects.
You will serve as the central safety contact for all engineering projects, acting as a key influencer and change agent across geographies and functions.

Who you will work with:
You will collaborate with diverse engineering teams and stakeholders worldwide. You are going to engage with colleagues at all levels, fostering open dialogue and trust, and ensuring safety is at the heart of every project.

What you will do:

You will champion a “Safety First” mindset and act as a role model for safe behaviors.
You will be responsible for developing and delivering impactful safety campaigns and awareness programs.
You will manage the integration of safety into design, planning, and execution phases of engineering projects.
You will lead root cause analysis of incidents, focusing on learning and sharing best practices.
You will ensure compliance with all relevant safety regulations and maintain up-to-date safety documentation.
You will drive continuous improvement by monitoring safety culture indicators and proposing actionable improvements.
You will ensure that safety is integrated into every stage of engineering—from design concept through project execution and operational handover.
You will lead or oversee key safety methodologies such as HAZID (Hazard Identification), HAZOP (Hazard and Operability Studies), and risk assessments during the design phase.
You will guide teams through root cause analysis (RCA) processes with a focus on systemic learning, not individual blame.
You will monitor and analyze safety culture indicators (e.g., near-miss reporting, campaign engagement) to proactively identify gaps and drive improvement actions.
You will maintain critical safety documentation such as incident reports, safety plans, and regulatory compliance records in line with local and international standards (GxP, ISO, OSHA).

Interested? For this role, we are looking for the following education, experience, and skills:

Bachelor’s degree or higher in a relevant field; PMI or equivalent certification preferred.
5+ years in safety leadership roles within engineering or industrial environments.
Proven track record in driving cultural change and influencing behaviors.
Strong interpersonal and communication skills to engage diverse teams.
Ability to lead through influence rather than authority, with knowledge of behavioral safety principles.
Experience in hazard identification, risk assessment, and change management.
Experience collaborating in complex, matrixed environments and influencing stakeholders without direct authority.
Knowledge of global regulatory frameworks and behavioral safety principles.
Comfortable navigating ambiguity and driving cross-functional alignment around safety strategy.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Learning Partner Patient Supply (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Learning Partner who is curious, relationship‑driven and solutions‑oriented to join our Talent and Company Reputation team, based in Braine l’Alleud, in Belgium.

About the role

You will be working in a team that strengthens the learning culture across Patient Supply. In this role, you will partner with business leaders and talent teams to design, deliver and improve learning experiences that help colleagues build the capabilities they need to grow and succeed. You will manage the full learning cycle—from identifying needs to implementing solutions and measuring impact—ensuring all learning initiatives align with business goals and global learning standards.

Who you’ll work with

Reporting to a more senior Learning Partner for Patient Supply, you will collaborate closely with learning partners, learning operations, talent partners, subject matter experts and business stakeholders across Patient Supply. Together, you will co‑create learning solutions, champion capability development and ensure that learning initiatives are relevant, high‑quality and smoothly deployed.

What you’ll do

Partner with business stakeholders to identify capability gaps and translate needs into learning plans that align with strategic priorities.
Build strong relationships with learning teams, talent partners and subject matter experts to co‑create impactful learning experiences.
Develop and propose learning solutions by leveraging existing global resources or commissioning new content when required.
Manage learning projects end‑to‑end, from needs assessment to design, pilot, implementation and continuous improvement.
Coordinate with learning operations teams to ensure smooth delivery, issue resolution and optimal learner experience.
Gather, interpret and share insights from learning data to guide improvements and measure progress.

Interested? For this role we’re looking for the following education, experience and skills

Significant experience in learning and development, learning design or capability building.
Fluent in FR and EN. Experience in Pharma, BioPharma and/or production environment is a plus.
Strong stakeholder management skills with the ability to partner, influence and communicate clearly across teams.
Experience designing or delivering learning programs, including workshops or digital learning solutions.
Ability to gather and interpret data to inform decisions and measure impact.
Strong planning and project-management capabilities, with a focus on continuous improvement.
Learning and development certifications or training are considered an asset.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technicien.ne utilities (Braine L'alleud, Walloon Brabant, BE)

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Nous recherchons un/e Technicien.ne de Maintenance Utilities qui est minutieux/se, proactif/ve et collaboratif/ve pour nous rejoindre sur notre campus de Braine-l'Alleud, Belgique.

À propos du rôle

En tant que Technicien.ne de Maintenance Utilities, vous serez responsable des interventions techniques et des améliorations dans le cadre de la maintenance des installations utilities du site de Braine, en suivant les règles établies dans le cadre de la GMAO. Vous travaillerez en horaire de jour, avec possibilité de rôle de garde.

Avec qui vous allez travailler

Vous collaborerez avec une équipe dynamique au sein du département Support Services. Ensemble, vous travaillerez en étroite collaboration avec les utilisateurs pour améliorer et développer les installations utilities. Vous interagirez également avec diverses parties prenantes pour assurer le bon fonctionnement et la maintenance des équipements.

Ce que vous allez faire

Vous participez aux améliorations et développements des installations Utilities.
Vous effectuez la maintenance préventive et curative des équipements.
Vous signalez toute anomalie, erreur ou incident à la hiérarchie.
Vous préparez et rédigez des instructions de maintenance et des dossiers techniques.
Vous assurez la documentation pré et post opérations de maintenance.
Vous suivez les règles GMP et GLP et maintenez les normes de sécurité et environnementales.

Intéressé/e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes

Minimum un A2 dans le domaine technique avec minimum 2 ans d’expérience dans la maintenance d’équipements ou un bachelier en électromécanique.
Expérience antérieure dans une société pharmaceutique ou agro-alimentaire souhaitée.
Connaissance des utilities (vapeur, eau, chauffage, ventilation) et techniques du froid.
Capacité à lire et interpréter des dessins électriques, mécaniques, pneumatiques et hydrauliques.
Très bonne connaissance du français ; connaissance pratique de l'anglais technique est un plus.
Pragmatique, rigoureux et capable de travailler en autonomie.
Bon esprit d'équipe et compétences communicationnelles.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technicien.ne utilities (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

Nous recherchons un/e Technicien.ne de Maintenance Utilities qui est minutieux/se, proactif/ve et collaboratif/ve pour nous rejoindre sur notre campus de Braine-l'Alleud, Belgique.

À propos du rôle

Avec qui vous allez travailler

Ce que vous allez faire

Vous participez aux améliorations et développements des installations Utilities.
Vous effectuez la maintenance préventive et curative des équipements.
Vous signalez toute anomalie, erreur ou incident à la hiérarchie.
Vous préparez et rédigez des instructions de maintenance et des dossiers techniques.
Vous assurez la documentation pré et post opérations de maintenance.
Vous suivez les règles GMP et GLP et maintenez les normes de sécurité et environnementales.

Intéressé/e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes

Minimum un A2 dans le domaine technique avec minimum 2 ans d’expérience dans la maintenance d’équipements ou un bachelier en électromécanique.
Expérience antérieure dans une société pharmaceutique ou agro-alimentaire souhaitée.
Connaissance des utilities (vapeur, eau, chauffage, ventilation) et techniques du froid.
Capacité à lire et interpréter des dessins électriques, mécaniques, pneumatiques et hydrauliques.
Très bonne connaissance du français ; connaissance pratique de l'anglais technique est un plus.
Pragmatique, rigoureux et capable de travailler en autonomie.
Bon esprit d'équipe et compétences communicationnelles.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

MSAT Bio DS Process Tech Transfer Expert (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a MSAT Bio DS Tech Transfer Expert who is detail-oriented, collaborative, and solution-driven to join our Bio Drug Substance Manufacturing Science and Technology team, based at our UCB campus located in Braine-l’Alleud, Belgium.

About the role

As a MSAT Bio DS Technology Transfer expert, you will support technology transfers and commercial-scale process validations for final mammalian biotechnological manufacturing processes. You will carry out a smooth and efficient transition between commercial manufacturing facilities as well as between Clinical Manufacturing and internal or external commercial manufacturing facilities, by providing the necessary documentation and ensuring compliance and optimal performance. You will also be responsible for driving continuous improvements and will play a key role as a technical expert throughout the product lifecycle.

Who you will work with

You will collaborate with cross-functional teams including Quality Assurance, CMC-Development, Industrial Leads, Analytical Transfer & QC Readiness teams. You will be also in contact with external partners and manufacturing sites, ensuring alignment and compliance across global operations.

What you will do

You will support technology transfer activities and implement process control strategies with stakeholders.
You will be responsible for writing risk assessments, protocols, and technical reports for Tech Transfer and validation runs.
You will manage coordination of sampling, analyses, and adherence to project timelines.
You will act as process expert post-transfer, owning documentation and supporting lifecycle management.
You will support Health Authority inspections and ensure compliance with cGMP requirements.
You will identify and implement process improvements and cost optimization initiatives within approved parameters.

Interested?

For this role, we are looking for the following education, experience, and skills:

Master’s degree in biology, biotechnology, or related life sciences field.
Strong understanding of biotechnological manufacturing processes and validation principles.
Excellent communication skills in English and French, both written and spoken.
Ability to manage complex projects, prioritize tasks, and make decisions under pressure.
Proficiency in MS Office tools and basic knowledge of statistics.
Strong leadership, problem-solving, and collaboration skills with a proactive mindset.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Infirmier.e service de santé interne à l'entreprise (CDD 7 mois) (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un/e Infirmièr/e Service Santé au travail (interne à l’entreprise) qui est organisée, fiable, empathique et proactif/ve pour nous rejoindre dans notre équipe des Services de Santé, basé sur notre campus de Braine-l'Alleud, Belgique.

À propos du rôle

En tant Infirmièr/e Service Santé, vous travaillerez en étroite collaboration avec le Médecin du Travail et les infirmiers seniors pour assurer la santé et la sécurité de nos employés sur trois sites : Braine-l'Alleud, Anderlecht et Leuven. Vous organiserez et suivrez les examens de surveillance de santé, réaliserez des visites de prévention de première ligne et administrerez les premiers soins aux victimes de malaises et d'accidents du travail.

Avec qui vous allez travailler

Vous ferez partie d'une équipe dynamique des Services de Santé, en collaboration avec le Médecin du Travail et les infirmiers seniors. Ensemble, vous veillerez au bien-être de nos employés, en travaillant en étroite collaboration avec les RH, le Service Interne de Prévention et de Protection, et d'autres intervenants.

Ce que vous allez faire

• Vous organisez et suivez les examens de surveillance de santé.

• Vous réalisez des visites de prévention de première ligne et administrez les premiers soins.

• Vous gérez le suivi administratif des accidents du travail.

• Vous offrez un soutien et des conseils aux employés pour des problèmes sociaux ou liés au travail.

• Vous participez au programme de retour au travail.

• Vous participez aux visites des lieux de travail et aux analyses de risques.

• Vous gérez les fournitures et équipements médicaux.

Intéressé ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes

• Diplôme d'infirmier avec expérience en premiers soins (secteur hospitalier, aide médicale urgente).

• Formation complémentaire en santé communautaire ou santé au travail est un plus.

• Maîtrise de la Suite Office et gestion de bases de données.

• Excellente connaissance du français et de l'anglais ; le néerlandais est un plus.

• Compétences organisationnelles et administratives solides.

• Empathie, précision et proactivité.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Pharmacometrics Lead Mechanistic Modeling - UK, Belgium or Germany (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Pharmacometrics Lead who is innovative and agile to join us in our Quantitative Clinical Pharmacology group, based at our research site in Slough (UK), Braine (Belgium) or Monheim, Germany.

About the role

Leading and delivering the Pharmacometrics strategy to support development of our assets. extrapolation (where appropriate), dose selection, trial design, PIP development and ongoing evaluation of data as generated.
Performing hands-on PBPK, QSP, and clinical trial simulations on an assigned project.
Transform PBPK and QSP analyses into actionable insights and communicate these findings effectively to project teams and stakeholders.
Developing submission ready fit for purpose Pharmacometrics analysis plans and reports.
Initiating and overseeing outsourced pharmacometrics activities and further internalizing the work as needed.
Supporting the development of a team from both a technical and scientific perspective to ensure state-of-the-art mechanistic approaches are applied to optimize drug discovery and development.
Having a working knowledge about regulatory pathways on a global basis and opportunities for collaboration with health authorities (either through working parties, advice meetings, and other initiatives) in pediatrics, Neurology and Immunology.
Promoting MID3 internally and externally.

Who you'll work with

Reporting to the Global Head of Pharmacometrics, you will be working closely with the QCP Leads assigned to the various projects, to ensure clear integration of the pharmacometrics aspects into the programs. Also with IT to ensure appropriate system validation and integration with other software is enabled.

Interested? For this role you’ll need the following education, experience and skills

Doctorate (PhD or MD) in related disciplines of Pharmaceutical Sciences, Statistics or Engineering with at least 6 years in PBPK and QSP modeling in (Bio)pharmaceutical industry.
Hands on expertise in PK-Sim® / MoBi®, SimCyp®, GastroPlus®, MatLab and R. Hands on experience with NONMEM and python is an additional advantage.
Hands-on experience in population PK/PD modeling is desirable.
Agile mindset with a proven ability to adjust by prioritizing multiple tasks.
Outstanding communication, organizational and presentation skills.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technical Compliance Specialist - Safety Equipment (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

Nous recherchons un.e Technical Compliance Specialist - Safety Equipment qui est rigoureux.se, autonome et engagé.e pour nous rejoindre sur notre site de Braine-l’Alleud, Belgique.

À propos du rôle

Vous êtes passionné.e par la conformité réglementaire et la sécurité ? Vous jouerez un rôle clé dans le suivi des inspections légales sur l’ensemble des sites belges d’UCB. Grâce à votre expertise, vous contribuerez à la sécurité des personnes et des biens, à la qualité des infrastructures et à la protection de l’environnement.

Avec qui vous allez travailler

Vous collaborerez étroitement avec les équipes HSE, Engineering, Maintenance et les responsables techniques des équipements. Vous serez rattaché.e au Team Leader Asset Compliance Légale et évoluerez dans un environnement dynamique et réglementé.

Ce que vous allez faire

Vous définissez et planifiez les contrôles légaux périodiques
• Vous supervisez les inspections avec les organismes agréés
• Vous rédigez les instructions et rapports de conformité (planification, suivi et reporting des controles légaux)
• Vous assurez le respect des procédures de sécurité et qualité
• Vous mettez en place des boucles d’amélioration continue
• Vous animez les FUP pour les owners équipements (conformité, deadlines) et apportez votre expertise technique aux équipes opérationnelles
Vous êtes l'assistant du Team Leader et gérer les activités day to day de l'équipe.

Intéressé.e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes

Formation technique ou scientifique (ingénieur industriel ou équivalent), minimum 5 ans d’expérience relevante, background technique et expérience en inspection légale indispensables (3 à 4 ans).
Maitrise des exigences légales belges, normes GMP et obligations liées aux inspections périodiques
Une maitrise des réglementations en électricité basse et haute tension, ainsi que des normes ATEX est un plus
Expérience en tant que Team Leader ou en gestion d'équipe
Expérience en environnement réglementé (pharma, chimie, agroalimentaire)
Connaissance des équipements industriels (HVAC, utilités, production)
• Maîtrise du français et de l’anglais
• À l’aise avec les outils informatiques (Maitrise d’Excel, SAP ou autre ERP, Sharepoint ou autres outils de documentation).

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Global Datacenter Corporate Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Global Datacenter Corporate Lead who is customer-focused, collaborative, and proactive to join us in our IT Infrastructure team, based in our Braine-l’Alleud site in Belgium.

About the role

You will be working in a team that ensures the quality and efficiency of datacenters services. You will manage transition of services management to the current service delivery framework. You will act as the main operational contact for external partners, manage service delivery performance, and champion continuous improvement. Your role includes designing and improving service management processes, monitoring KPIs, and ensuring compliance with agreed service levels. This global role requires strong governance, strategic relationships, and a focus on operational excellence.

Who you’ll work with

You will collaborate with internal teams, offshore resources, and external vendors to ensure seamless service delivery. You will engage with stakeholders across IT and business functions, building strong partnerships and driving improvements in service quality.

You will work closely with the operation managers who manage the deliveries and services requests.

Aligning with demand and engagement manager to ensure perfect delivery within the standard and agreed planning.

You will work in a dynamic, international environment that values innovation and teamwork.

What you’ll do

Design and improve service management processes for IT datacenter services
Act as the main operational contact for external partners and vendors
Monitor and report on service quality, KPIs, and compliance with SLAs
Drive operational improvements and continuous service optimization
Establish governance and strategic relationships for stable, cost-efficient services
Coordinate resource requests, including people, environments, and licenses.

Interested? For this role we’re looking for the following education, experience and skills

Master’s degree in IT or related field
5–10 years of experience in IT service delivery management
Strong knowledge of service management frameworks and best practices
Excellent communication and stakeholder management skills
Ability to prioritize, problem-solve, and drive improvements in a global context
Fluent in English, French or Dutch are a plus
A positive mindset, eager to learn and appetite for innovation

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Asset Legal Compliance Specialist (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un.e Asset Legal Compliance Specialist qui est rigoureux.se, autonome et engagé.e pour nous rejoindre sur notre site de Braine-l’Alleud, Belgique.

À propos du rôle

Avec qui vous allez travailler

Ce que vous allez faire

Vous définissez et planifiez les contrôles légaux périodiques
• Vous supervisez les inspections avec les organismes agréés
• Vous rédigez les instructions et rapports de conformité (planification, suivi et reporting des controles légaux)
• Vous assurez le respect des procédures de sécurité et qualité
• Vous mettez en place des boucles d’amélioration continue
• Vous animez les FUP pour les owners équipements (conformité, deadlines) et apportez votre expertise technique aux équipes opérationnelles.

Intéressé.e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes

Formation technique ou scientifique (ingénieur industriel ou équivalent), minimum 3 ans d’expérience relevante, background technique et expérience en inspection légale indispensables
Maitrise des exigences légales belges, normes GMP et obligations liées aux inspections périodiques
Expérience en environnement réglementé (pharma, chimie, agroalimentaire)
Connaissance des équipements industriels (HVAC, utilités, production)
• Maîtrise du français et de l’anglais
• À l’aise avec les outils informatiques (Maitrise d’Excel, SAP ou autre ERP, Sharepoint ou autres outils de documentation).

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

UCB est une société biopharmaceutique mondiale, spécialisée dans la neurologie et l'immunologie. Nous sommes environ 8 500 personnes aux quatre coins du monde, inspirées par les patients et motivées par la science.  

Pourquoi travailler pour nous ?

Global Logistics Suppliers Partnership Manager (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Global Logistics Suppliers Partnership Manager who is collaborative, strategic, and solutions-oriented to join our Global Logistics team, based at our UCB campus located in Braine-l'Alleud, Belgium.

About the Role:

Reporting to the Global Logistics Network Lead, you will be at the forefront of developing and managing relationships with Logistics Service Providers (LSPs), including transportation partners, 3PLs, 4PLs, warehouses, and brokers. Your mission: to ensure robust supplier performance, supply continuity, and best-in-class delivery of goods across global markets while aligning with UCB’s evolving business needs.

What You'll Be Doing:

Act as a key liaison between UCB and its global logistics providers to drive strong partnerships and ensure consistent performance.
Lead Quarterly and Annual Business Reviews with key LSPs to assess KPIs, service quality, and cost performance. Identify gaps, escalate critical issues, and implement action plans.
Support tendering, supplier onboarding, and vendor selection processes in close collaboration with Procurement and Quality.
Proactively monitor supplier SLAs, anticipate supply chain risks, and implement mitigation strategies to safeguard business continuity.
Drive cross-functional coordination for logistics-related projects, including new product launches, ensuring efficient and compliant implementation.
Partner with UCB’s Lead Logistics Provider (LLP) to analyze trends and anticipate business needs.
Champion continuous improvement initiatives, capturing internal and external feedback to enhance service levels, productivity, and supplier capabilities.
Conduct risk assessments and regular due diligence activities across the LSP network.
Collaborate on strategic governance for LSPs and help standardize governance programs across the Global Logistics Network.

Who You Will Work With:

You’ll operate cross-functionally with:
- Internal teams across Global Distribution, Supply Chain, Quality, and Procurement
- External partners including 3PLs, 4PLs, carriers, customs brokers, and industry vendors

Interested? For this role, we are looking for the following education, experience, and skills:

A Bachelor’s or Master’s degree in Supply Chain, Business, Engineering, or related field
5+ years of experience in logistics, warehousing, or transportation (global scope preferred)
3+ years in the pharma, medical devices, or FMCG sectors
Solid understanding of GDP compliance and distribution regulations
Certifications in Six Sigma, Lean, or APICS are a strong plus
Fluent in English (French and other languages are a plus)
Strong skills in stakeholder management, influencing, and conflict resolution
Analytical mindset with a knack for KPIs, numbers, and performance metrics
Proven ability to work autonomously and manage complex global relationships
High proficiency in SAP, TrackWise, and MS Office tools
Agile, solution-oriented, and comfortable working in a multicultural, matrixed environment

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Technicien.ne Contrôle ZAC/Salle Blanche (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un.e Technicien.e Contrôle ZAC/Salle Blanche qui est rigoureux.se, autonome et team player pour nous rejoindre dans notre équipe basée sur notre site de Braine-l’Alleud, Belgique.

À propos du rôle
Vous assurez le suivi et la réalisation des contrôles périodiques des salles blanches et équipements à flux d’air. Vous prenez en charge l’ensemble des activités liées à ces contrôles, en veillant à la conformité, à la qualité et à l’amélioration continue des processus.

Avec qui vous allez travailler
Vous collaborez avec les équipes QA, Qualification, utilisateurs, ainsi qu’avec des sous-traitants externes. Vous coordonnez vos activités avec d’autres départements pour atteindre les objectifs des projets dans un environnement stimulant et exigeant.

Ce que vous allez faire
• Vous gérez votre planning et toutes les activités de contrôles des salles blanches
• Vous participez aux réunions de projet et de coordination
• Vous suivez et respectez le planning des contrôles
• Vous gérez et coordonnez les sous-traitants externes
• Vous exécutez et suivez les chantiers et les tests sur le terrain
• Vous défendez les dossiers lors des audits et assurez l’amélioration continue

Intéressé ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes
• Bachelier (préférence électromécanique, métrologie, automation, ...) avec une expérience probante de min 10 ans
• Expérience en GMP et industrie pharmaceutique
• Capacité à travailler en équipe et de manière autonome
• Bonne connaissance des outils informatiques
• Connaissance de l’anglais (parlé et écrit)

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Technicien.ne Contrôle ZAC/Salle Blanche (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Business Solution Expert Manufacturing Systems (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Business Solution Expert Manufacturing Systems ( SAP PPI / OMP DS ) who is strategic, digital minded, and collaborative to join our Internal Manufacturing Digitalization team, based at our UCB campus located in Braine-l'Alleud, Belgium.

About the role

You’re going to play a pivotal role in transforming UCB’s internal manufacturing operations through digitalization. You will lead both the operational excellence of our manufacturing systems and the strategic roadmap for SAP PP/PI and OMP DS platforms.

Who you will work with

You will collaborate with Site Operations Leads, Process Experts, Manufacturing Excellence teams, and Digital Technology partners. You’ll also lead a community of Local Key Users and engage cross-functionally with Quality Assurance and other enterprise stakeholders.

What you will do

As Business Solution Expert / Process Data Owner (PDO):

You will lead solution design and ensure systems support global manufacturing processes.
You will manage system deployments and change requests across project and run modes.
You will chair the Local Key User community and foster knowledge sharing.
You will ensure compliance with UCB’s Computerized System Validation (CSV) procedures.
You will oversee testing, documentation, and user training to ensure solution adoption.
You will monitor operational performance and support incident and change management.

As SAP PP/PI & OMP DS Lead:

You will co-create the digital manufacturing roadmap aligned with strategic priorities.
You will act as delivery lead for key deployment programs and ensure governance adherence.
You will stay ahead of technology trends and recommend best practices.
You will drive value realization through performance monitoring and system audits.
You will ensure seamless integration of SAP PP/PI and OMP DS with enterprise systems.
You will partner with stakeholders to identify opportunities for process and data optimization.

For this role, we are looking for the following education, experience, and skills

Master’s degree in Business, Engineering, Life Sciences, or Information
Proficiency in SAP S/4 Suite, including SAP Enable Now, BTP, and GRC.

Technology

Proven experience with SAP PP/PI (ECC or S/4) and OMP DS in a global manufacturing environment.
Strong understanding of biopharma manufacturing planning and execution processes.
Excellent project leadership, stakeholder engagement, and problem-solving skills.
Fluent in both French and English, with a data-driven and analytical mindset.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

System Automation SME (subject matter expert) (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a System Automation SME who is detail-oriented, collaborative, and solution-driven to join our team, based in our Braine-l'Alleud office in Belgium.

About the role

You will play a key role in delivering automation expertise across our manufacturing facilities in Belgium. You’ll ensure quality, compliance, and efficiency in automation deliverables throughout the project lifecycle.

Who you’ll work with

You’ll collaborate closely with automation integrators, production, maintenance, quality, and engineering teams to ensure smooth coordination and optimal outcomes.

What you’ll do

You develop and maintain automation documentation and software.
• You attend workshops and align project disciplines.
• You follow up with automation integrators and vendors.
• You verify deliverables and anticipate cost increases.
• You ensure GMP and HSE compliance.
• You organize operator training and handover to operations.

Interested? For this role, we’re looking for the following education, experience, and skills

Bachelor or Master degree in automation.
• Minimum 5 years’ experience in GMP process automation.
Strong knowledge of PCS7.
• Fluent in French and English.
• Strong design, execution, and validation skills.
• Excellent communication and leadership abilities.
• Risk management and adaptability in dynamic environments.

Be part for 24/7 guard support in hybrid model with Automation Integrators and ready to travel a limited period of time.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Automation Engineer (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for an Automation Engineer who is detail-oriented, collaborative, and solution-driven to join our team, based in our Braine-l'Alleud office in Belgium.

Note that 3 roles are now open : 1 specialized in PCS7 (system engineer), 1 in Aveva SP (facilities engineer) and 1 specialized in PCS7 and Aveva (alarm engineer).

About the role

Who you’ll work with

You’ll collaborate closely with primarily Production, followed by Quality teams (QA and Qualification), and finally IT for compliance with cybersecurity and virtualization regulations in order to ensure smooth coordination and optimal outcomes.

Major projects you could participate in

PCS7: We have 4 infrastructures in Belgium where PCS7 is used,in which there are numerous projects such as the implementation of new molecule production, new equipment, and production optimizations. We also have upgrade projects to keep installations up to date.
AVEVA SP: Projects to redefine all our infrastructures to integrate new buildings and installations: site utilities and new research facilities.

What you’ll do

•You attend workshops and align project disciplines.

•You develop and maintain automation documentation and software.
• You follow up with automation integrators and vendors.
• You verify deliverables and anticipate cost increases.
• You ensure GMP and HSE compliance.
• You organize operator training and handover to operations.

Evolution in the role

BelTech Automation was officially created in January 2025. It is a team under construction and expansion, with the ambition to align our support models for production and projects in Belgium.

This could lead to growth opportunities in technical, project, and management areas. The team currently consists of 15 internal members and more than 80 external collaborators.

Interested? For this role, we’re looking for the following education, experience, and skills

Bachelor or Master degree in automation.
Minimum 5 years’ experience in GMP process automation.
Strong knowledge of PCS7 and/or AVEVA SP
Fluent in French and English.
Strong design, execution, and validation skills.
Excellent communication and leadership abilities.
Risk management and adaptability in dynamic environments.

Be part for 24/7 guard support (level 2) in hybrid model with Automation Integrators, and ready to travel a limited period of time.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Secondary Packaging Industrialization Expert (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Secondary Packaging Industrialization Expert who is detail-orientated, collaborative and adaptable to join our Devices, Packaging & Wearables Technology team, based in our campus in Braine-l'Alleud, Belgium.

About the role

You will contribute to the development, validation, and industrialization of secondary and tertiary packaging components across UCB’s global packaging operations, supporting both development and commercial activities. You will manage key processes including defining packaging user requirement specifications, validating designs, overseeing industrialization workflows, preparing technical drawings for artwork, and maintaining the technical database for global commercial products. This role does not include responsibilities related to shipping qualifications or cold chain development activities.

What you’ll do

Lead packaging projects from design to industrialization and lifecycle management.
Provide technical support to sites, affiliates, and external partners.
Manage projects, change controls, and stakeholder communications.
Apply packaging regulations and standards in development and manufacturing.
Optimize and troubleshoot packaging activities across manufacturing environments.
Contribute to team goals, planning, and process improvements.
Lead small projects or support complex multi-site initiatives.
Guide tech transfers, validations, and investigations for packaging projects.
Coordinate packaging communications with one or two designated sites.

Interested? For this role we’re looking for the following education, experience and skills

Experience working in secondary and tertiary packaging manufacturing
Strong background in GMP operations and compliance
Familiar with pharmaceutical projects like tech transfers and product launches
Able to manage multiple priorities and projects effectively
Comfortable working in cross-functional teams and leading projects
Proficient in English (written and spoken)

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Ethics & Business Integrity Manager (Germany and ALPs) (Monheim, Mettmann, DE)

Make your mark for patients

We are looking for an Ethics & Business Integrity Manager who is proactive, collaborative, and solutions-driven to join our Ethics & Business Integrity team. The preferred location is our office in Monheim/Germany, alternatively the office in Vienna/Austria.

About the role

Approximately 70% of your time will be dedicated to maintaining and operationalizing our Ethics & Business Integrity program in Germany. This includes managing compliance risks, supporting business stakeholders, and fostering an ethical, compliant culture across the organization. You will ensure adherence to local industry regulations while contributing to global initiatives that strengthen our overall compliance framework. The remaining 30% of your time will be devoted to driving and supporting the Ethics & Business Integrity program in the ALPs region (Austria & Switzerland).

Who you’ll work with

You will partner with business stakeholder in Germany and across the ALPs, working closely with key local functions such as Legal and Medical Affairs, while reporting to the Business Integrity Lead Germany. In this highly collaborative role, you will advise colleagues on healthcare interactions, shape compliance standards, and contribute to a strong culture of ethics across the organization. You will also represent UCB in external industry associations, ensuring we stay ahead of evolving regulatory and industry trends.

What you’ll do

Implement and maintain local compliance policies, procedures, and programs in line with regulations and codes.
Perform compliance risk management and oversee due diligence processes for outsourced activities.
Perform field- and/or desk- monitoring activities as described in the annual plan.
Deliver Ethics & Business Integrity training to employees and third parties.
Support audits and reviews, ensuring corrective actions are implemented effectively.
Advise business stakeholders on ethical practices and foster a compliance-driven culture.
Participate in local industry trade groups to maintain regulatory awareness.
Participate in ALPs Leadership team meetings.

Interested? For this role we’re looking for the following education, experience and skills

Bachelor’s degree required; Master’s degree preferred.
CCEP/CCP-I Certification or alternative E&BI education program is an advantage.
Ideally 2 years of experience in healthcare regulatory or consulting roles.
Knowledge of healthcare regulatory standards and compliance best practices.
Strong communication skills and ability to build trust across all levels.
Fluent in German and English and/or French is a plus.
Ability to work independently, solve problems, and collaborate in a cross-functional environment.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

EU Evidence Generation Lead - Rare Diseases & Epilepsy (m/f/d) (Monheim, Mettmann, DE)

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We are looking for an EU Evidence Generation Lead Developmental Epileptic Encephalopathies and Epilepsy (m/f/d) who is strategic, collaborative, and highly self-driven to join us in our Rare Diseases & Epilepsy team, based in Monheim, Germany.

About the role

Who you’ll work with

What you’ll do

Build and maintain strong relationships with external partners and EU country teams
Oversee development and execution of evidence generation plans in key markets
Drive delivery of EU-level projects, ensuring timelines, budgets, and quality standards
Represent UCB at scientific forums and with regulatory and reimbursement bodies
Champion innovative digital solutions to enhance evidence generation
Lead capability building and training for EU teams
Collaborate across matrix teams and work independently to achieve objectives

Interested? For this role we’re looking for the following education, experience and skills

Bachelor’s degree with relevant professional experience required; Master’s or PhD preferred
5+ years’ experience in evidence generation, preferably in epilepsy or rare diseases
Proven ability to thrive in a complex matrix organization
Demonstrated team player with excellent collaboration skills, yet highly self-driven and able to work independently
Strong understanding of healthcare ecosystems and policy shaping
Excellent communication and relationship-building skills
Digital literacy and agile mindset

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Trainee Marketing Rare and Epilepsy (m/f/d) (Monheim, Mettmann, DE)

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We are looking for a Trainee Marketing Rare & Epilepsy (m/f/d) for our location in Monheim am Rhein, to start as soon as possible. This position is limited to 2 years, working as an integral member of our marketing team in Germany.

About the role

The primary purpose of this role is to take responsibility for Marketing, commercial and medical projects within the Marketing Team Rare & Epilepsy. This includes own projects as well as supporting the Marketing Leads and Marketing Managers in aligning and developing solutions, such as projects, activities, and patient programs.

This role is not a traditional traineeship. From day one, you will become a full member of a dedicated team and take on meaningful operational tasks within a defined functional area. You will actively contribute to concrete projects and day‑to‑day activities while gaining hands-on experience in a professional environment. The position is offered as a fixed-term entry role designed to give you a solid start into your career.

Who you´ll work with

The role involves driving the localization and implementation of the strategy in collaboration with the cross-functional team in Germany. It requires strong collaboration skills with all internal and external stakeholders.

This position reports to the Head of Marketing Rare & Epilepsy and is part of the Rare & Epilepsy Germany Team.

What you´ll do

Engage and manage external agencies/vendors to successfully implement initiatives within budget and agreed timelines
Orchestrate material management and exchange with EU stakeholders
Lead congress projects in close collaboration with event management, medical and external stakeholders
Champion concept development of digital solutions for all stakeholder groups
Value and impact measurement with the Strategy Lead, Solution Lead, and Business Capability Partner (e.g. developing, monitoring, and tracking KPIs)
Development and implementation of solutions to enhance patient benefits in cooperation (e.g., national F2F events, national billboards, online and offline services and tools for patients and healthcare representatives)

Interested? For this role we’re looking for the following education, experience and skills:

Successfully completed studies in the field of medicine, biology (PhD preferred), marketing, communication or a comparable education
Demonstrated excellence in written and verbal communications
Initial work experience in relevant areas is an advantage
Interest in data-driven marketing and analytical skills to make informed decisions
Excellent organizational skills as well as a structured and independent working style
High level of team spirit, motivation, and proactivity
Fluent in German and English

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Principal Statistician (Germany) (Monheim, Mettmann, DE)

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We are looking for a Senior Principal Statistician to join us in our Biometrics & Data Science team, based in any of our Brussels (Belgium), Monheim (Germany) or Slough (UK) offices.

About the role

Who you’ll work with

You will report into the Head of Early Development Statistics or a technical area leader in her team (Translational Statistics lead, or Clinical Pharmacology Statistics Lead)

What you’ll do

Provide direction and continuous leadership of the Early Development Statistics team – for compounds under development, via an expert area such as clinical pharmacology statistics, pre-clinical, biomarker and or bioassay development.
Lead and influence the translation of strategy to tactical planning, operations, and quality
Contribute to strategic planning of the non-clinical and or clinical development plan, including study designs, design of experiments, analysis plans, quantitative decision criteria, exploratory analysis etc.
May oversee more junior statisticians, to ensure operational delivery of statistical outputs, for clinical or non-clinical studies.
Work closely with relevant stakeholders in the team, such as research lead, biomarker lead, bioassay development lead or quantitative clinical pharmacology lead, in alignment with statistics leaders such as Project Lead Statistician, translational statistician, or clinical pharmacology statistician.
Help lead the continuous learning and upskilling culture for a modern Biometrics (statistics) organization

Interested? For this position you’ll need the following education, experience and skills:

MSc. Or Ph.D. in Biostatistics or Statistics, or equivalent
More than 5 years in the pharmaceutical industry;
Solid knowledge of drug development across all phases.
Experience in Early Development, in at least one technical area (pre-clinical, translational (biomarker/bioassay), or clinical-pharmacology)
Understands how the functional expertise and contributions fit into the bigger picture
Influencer and collaborator in a development team environment
Good communication skills
Programming skills in R or SAS

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Pharmacometrics Team Lead (Germany) (Monheim, Mettmann, DE)

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About the role

Who you’ll work with

Working closely with the QCP Leads assigned to the various projects, to ensure clear integration of the pharmacometrics aspects into the programs.

What you’ll do

Coaching and mentoring junior staff on how to navigate within a project and matrix organization.
Leading and delivering the Pharmacometrics strategy to support development of our assets. extrapolation (where appropriate), dose selection, trial design, PIP development and ongoing evaluation of data as generated.
Performing hands-on population PK/PD, exposure-response modeling and clinical trial simulations on an assigned project.
Developing submission ready fit for purpose Pharmacometrics analysis plans and reports.
Initiating and overseeing outsourced pharmacometrics activities and further internalizing the work as needed.
Having a working knowledge about the regulatory pathways on a global basis and opportunities for collaboration with health authorities (either through working parties, advice meetings, and other initiatives) in pediatrics, Neurology and Immunology.
Promoting MID3 internally and externally.

Interested? For this role you’ll need the following education, experience and skills

Doctorate (PhD or MD) in the related disciplines of Pharmaceutical Sciences, Statistics or Engineering.
8+ years (Bio)pharmaceutical industry experience in Pharmacometrics with minimum of 2 years line management responsibilities.
Hands-on experience in population PK/PD, disease progression modeling, and clinical trial simulations.
Strong understanding and knowledge of Bayesian methodologies, model-based meta-analyses, PBPK, QSP, and AI/ML in Pharmacometrics.
Expertise in R, NONMEM or related pharmacometrics software.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Order to Cash Accountant (Monheim, Mettmann, DE)

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Order to Cash Accountant

We are looking for an Order to Cash Accountant who is detail‑oriented, proactive, and collaborative to join us in our Finance team, based in our Monheim office in Germany.

About the role

You will be working in a team that ensures accurate and compliant Order to Cash operations for our activities in Germany and Austria. In this role, you will manage customer accounts, payment processes, and compliance reporting while acting as a key point of contact for internal and external stakeholders. You will work independently within defined guidelines and contribute your expertise to drive continuous improvements across finance processes.

Who you’ll work with

You will be working in a team that collaborates closely with local and global finance functions, including credit management, treasury, and our outsourced accounting partner. You will engage with pharmacies, banks, and internal auditors, contributing to a professional, multicultural, and supportive environment focused on accuracy, service, and compliance.

What you’ll do

Manage day‑to‑day accounts receivable activities, including customer reconciliations and dunning processes.
Coordinate payment processes, manual payments, and banking activities for Germany and Austria.
Prepare required regulatory reports, including national bank reporting and compliance submissions.
Collaborate with and supervise outsourced teams handling direct debit and cash allocation tasks.
Support internal and external audits and ensure all reconciliations are accurate and up to date.
Identify opportunities for process improvements and contribute to global finance projects.

Interested? For this role we’re looking for the following education, experience and skills

Certified Accountant qualification or several years of accounting experience in a multinational environment.
3–5 years of relevant experience in accounting, ideally within Order to Cash.
Strong technical accounting knowledge, especially German GAAP; International Financial Reporting Standards knowledge is a plus.
Strong systems knowledge, including Excel, enterprise resource planning systems (SAP), and reporting tools.
Strong analytical skills with the ability to interpret and report data accurately.
Fluent spoken and written German and good English communication skills.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Senior Project Lead Programmer (Germany) (Monheim, Mettmann, DE)

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About the role

Who you’ll work with

You will report into the Head of Programming Visualisation & Reporting

What you’ll do

Define and implement the programming team’s open-source innovation strategy aligned with the department goals.
Develop the vision and roadmap for open-source tools that directly support the Biometrics department, including programming, visualization, and reporting needs but not limited to.
Drive innovation in clinical trial analyses, using R to improve the efficiency of study results analysis delivery for the Programming team
Champion open-source principles across departments including R&D, IT, Regulatory Affairs, and Data Science.
Represent the company in external open-source consortia (e.g., Pharmaverse, PHUSE, etc.).
Responsible to lead high complex projects with multiple stakeholders (internal and external stakeholders) and articulated structure Lead and shape the continuous learning and upskilling culture for a modern Biometrics (Programming) organization

Interested? For this position you’ll need the following education, experience and skills:

MSc (preferred) in Statistics, Mathematical, Statistical Computer Science or Life Science, or equivalent
Deep understanding of open-source ecosystems, licensing models, and software development practices
Strong communication and stakeholder management skills across scientific and technical domains.
Experience with regulatory environments and data standards (e.g., CDISC, HL7).
Proficiency in platforms like GitHub and tools such as R, Python, Docker, and CI/CD pipelines.
Experience contributing to or leading open-source projects in clinical research or statistical programming.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Clinical Development Lead (Germany) (Monheim, Mettmann, DE)

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About the role

Who you’ll work with

What you’ll do

Set the global clinical development strategy for assigned asset(s), ensuring alignment with TPVP, regulatory requirements, and commercial goals.
Lead external engagement with global thought leaders, investigators, and stakeholders to continuously refine strategy based on emerging insights and unmet needs.
Design and adapt robust clinical development plans that integrate the latest scientific, regulatory, operational, and payer perspectives—balancing innovation with executional feasibility.
Oversee the execution of pivotal studies and regulatory submissions across all relevant markets, ensuring clinical excellence, data integrity, and timely delivery.
Shape clinical narratives and regulatory strategy, acting as a key representative in interactions with global health authorities and strategic partners.
Contribute to corporate strategy, supporting business development initiatives and representing the clinical perspective in asset evaluations.

Interested? For this position you’ll need the following education, experience and skills:

Advanced degree (MD, PhD, PharmD, or equivalent).
Track record of leading complex global programs across multiple indications.
Familiarity with digital health technologies, real-world data, and AI-enabled trial innovation.
Ability to lead through ambiguity, make informed decisions in uncertainty, and drive results across organizational boundaries.
Strategic mindset with a bias for innovation, speed, and operational excellence.
Exceptional communication and stakeholder management skills, including C-suite level.
Global experience and cultural fluency; willingness to travel internationally as needed.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Finance Director - Insight to Impact Lead Germany (m/f/d) (Monheim, Mettmann, DE)

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Finance Director – Insight to Impact Lead Germany (m/f/d)

We are looking for a strategic, performance‑driven and execution‑oriented Finance leader to join UCB as Finance Director – Insight to Impact Lead Germany (m/f/d), based in Monheim am Rhein, Germany.

In this role, you will sit at the heart of business decision making, combining financial leadership, strategic insight and performance management to ensure that UCB’s investments, priorities and execution deliver measurable value for patients and sustainable business performance.

About the role

In this senior leadership role, you will drive the short‑ and long‑term performance of UCB in Germany across all patient‑focused and go‑to‑market activities.

You will lead the German Insight to Impact (I2I) capability – UCB’s approach to turning data, analytics and financial insights into clear business decisions and tangible outcomes. I2I connects strategy, finance, performance management and execution, ensuring that resources are allocated where they create the greatest impact.

Acting as a trusted advisor and constructive challenger to the General Manager and Leadership Team, you will provide strategic, financial and operational insights to support evidence‑based decision making. You will be accountable for performance monitoring, insights generation, planning and resource allocation, while ensuring strong alignment with European and corporate priorities.

You will play a critical role in embedding a strong performance culture, strengthening governance, and building robust processes and data foundations that support sustainable growth and patient impact.

Who you’ll work with

You will be a key member of the German Leadership Team and part of a broader European Insight to Impact leadership community.
You will work closely with senior stakeholders across:
Commercial, Marketing and Sales
Medical and Market Access
Finance and FP&A
Digital,Data and Analytics teams

You will also provide direction and leadership to the local Insight to Impact team, ensuring strong delivery against local priorities while maintaining alignment with regional and global standards.

What you’ll do

Act as the senior finance and performance partner for the German General Manager and Leadership Team
Lead the Insight to Impact agenda in Germany, connecting strategy, finance and execution
Drive business performance management, translating strategy into clear financial and non‑financial outcomes
Generate and synthesize insights to support go‑to‑market effectiveness, product launches and portfolio prioritization, continuous performance improvement
Measure and monitor the business and patient impact of initiatives and investments
Play a central role in investment decisions and resource allocation, ensuring capital is deployed where it creates most value
Identify and recommend resource reallocation opportunities to improve efficiency and impact
Lead planning, forecasting and corporate cycle processes in close partnership with FP&A
Ensure high‑quality business narratives, reports and decision materials for senior leadership
Strengthen governance, processes and data foundations supporting performance management
Support digital and data‑driven transformation initiatives
Represent Germany in European Insight to Impact forums, contributing to cross‑country learning and alignment

Interested? For this role we’re looking for the following education, experience and skills

Extensive experience in finance, strategy or business performance roles, ideally within healthcare, life sciences or complex regulated industries
Strong track record partnering with senior leadership and influencing strategic and operational decisions
Proven ability to translate financial data and analytics into clear business insights
Experience in performance management, planning, forecasting and investment decision support
Strong understanding of commercial and go‑to‑market dynamics
Strategic and structured thinker with a strong execution mindset
Excellent stakeholder management and communication skills
Experience working in matrixed, international environments
Master’s degree in Finance, Business, Economics or a related field
Fluent English and strong professional proficiency in German

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Data Science Lead 1 (Monheim, Mettmann, DE)

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To strengthen our Global Advanced Analytics team, we are looking for an adaptable, collaborative individual with an intrapreneurial mindset for our Analytics Lead opening. This hybrid role is based in our headquarters in Monheim, Germany requiring 40% onsite presence and 5-10% international/ domestic travel.

What you’ll do

Analytics Leadership: Provide clear expertise for opportunities to leverage advanced analytics, especially where they are advantageous to reducing the need for primary data or have high marginal impact
Deliver the most impactful data and analytics projects that:

address the most compelling business questions, and/or
identify new opportunities for patients and UCB through effective visual displays of quantitative and qualitative information

Partnership and Collaboration: Be the key strategic partner for functional stakeholders and co-create plans and priorities for data and advanced analytics with them together with the Patient Solutions and Evidence Leads. Ensure tight relationships and collaboration with IT, Data Office, and other Analytics teams using relevant data sources.
Team Leadership. Serve as a mentor and guide to more junior data scientists and translators in demonstrating the application of cutting-edge analytics, clear communication and presentation of insights and practical/pragmatic implementation of key recommendations
Drive the execution of regional and local data-driven insights research and data analytics plans and priorities
Foster a strong data science community with significant business acumen and communication skills across Hubs and Engine and Supervise the conduct of advanced analytics studies in a collaborative manner ensuring that the study methodology is appropriate to deliver reliable results.
Improve the team’s partnership with, and impact on, key internal (UCB) and external stakeholders within the specific area of focus by:

developing and executing a communication and collaboration plan with key UCB stakeholders
increasing personal and the Advanced Analytics team’s knowledge of the business by ensuring that she/he and each team member has direct interaction with patients and/or other external stakeholders

Attract, retain, motivate, and develop key talent for the Advanced Analytics team; coach and develop team members
Drive deep partnership with the Hub insights team and other “fellow” Engines and insights generating functions (e.g. regional analytics teams) allowing for a joined delivery of cross-functional, deep impactful insights
Be a champion for a data-driven, decision-making culture

Interested? For this role we’re looking for the following education, experience and skills

Minimum Experience/Skills Required:

Bachelor's degree in quantitative area
Minimum of 8-10+ years experience applying predictive modeling techniques such as ML, decision trees, ensemble learning, neural networks etc, and data transformation such as data cleansing and integration, fuzzy matching, etc., is required
Minimum of 8-10+ years of experience developing program/project plans and leading programs/projects from initiation to implementation is required
At least 8 years of experience working with real world data (Claims data, EMR, IQVIA, -omics, etc)
Minimum of 8-10+ years of experience with programming and application development using Python or R is preferred

Preferred Experience/Skills:

Master/Doctor’s degree in quantitative area
Knowledge of pharmaceutical industry, ideally specialty pharma and biologic treatments
Deep expertise in leveraging data science methodologies within the Research and Development and Clinical trials sphere of the pharmaceutical industry. The Go-to-Market domain encompasses the commercial, medical, and market access facets of the business
Expertise in analyzing a range of large, secondary transactional databases, unstructured data or other computationally difficult challenges
You are a structured problem solver
Possess an 80/20 mindset to push for fast model iterations
Interpret model results and identify potential model errors (e.g., overfitting, model bias, correlation vs causation)
Global role, so willingness and flexibility to work across geographies / time zones (sometimes outside of core hours)

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Sales Representative (m/f/d) Dermatology - Magdeburg, Brandenburg, Potsdam, West‑Berlin, Schwerin, S (Monheim, Mettmann, DE)

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Sales Representative (m/f/d) Dermatology – Magdeburg, Brandenburg, Potsdam, West‑Berlin, Schwerin, Stralsund, Rostock & Greifswald

To strengthen our dermatology team, we are looking for a Sales Representative (m/f/d) for the region Magdeburg, Brandenburg, Potsdam, West‑Berlin, Schwerin, Stralsund, Rostock and Greifswald.

About the role
As a Sales Representative (m/f/d), you will be responsible for building, developing, and maintaining customer relationships, focusing on discussing our innovative therapies with private practitioners and clinics in your area.

Who you’ll work with
Together with your multi‑member sales team, you will establish reliable customer contacts through both in‑person visits and digital channels. For comprehensive scientific advice to your customers, you will coordinate with the medical field team and report to the ecosystem lead.

What does that mean specifically?

Building and expanding long‑term customer relationships in dermatology (clinic doctors, private practitioners, specialists, medical assistants, pharmacists)
Achieving sales and revenue goals and growing the product portfolio in the area
Regular maintenance and adherence to the communication plan
Active use of all available channels and materials for an individual multi‑channel customer journey
Active use of agile working methods
Active use of all available analysis tools, including digital assistant, advanced analytics, omnichannel customer journey, and persona segmentation

Interested? For this position, we are looking for the following qualifications, experience, and skills:

Completed training as a pharmaceutical representative (certification according to §75 AMG) and/or a completed scientific degree
Several years of experience in the field service for specialists and clinics; experience with biologics is an advantage
Excellent skills in conveying highly complex medical information
A high degree of self‑responsibility, integrity, and discretion
English and German language skills, both written and spoken
Permanent residence in the advertised area

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Trainee Business Analyst - Data & Insights (m/f/d) (Monheim, Mettmann, DE)

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Job Posting – I2I PI Business Analyst Graduate – Germany (m/f/d)

We are looking for an I2I PI Business Analyst Graduate who is curious, analytical and eager to learn to join our Insight to Impact (I2I) team, based in our Monheim office in Germany.

About the role

As a Business Analyst Graduate, you will support Business Analysts and key stakeholders across Immunology, Epilepsy, and Rare Diseases. You will contribute to data-driven decision-making, expand analytical maturity, and help strengthen cross-functional impact within the organization.

This role is not a traditional traineeship. From day one, you will become a full member of a dedicated team and take on meaningful operational tasks within a defined functional area. You will actively contribute to concrete projects and day-to-day activities while gaining hands-on experience in a professional environment. The position is offered as a fixed-term entry role designed to give you a solid start into your career.

Who you'll work with

You will collaborate closely with the I2I Area Lead, Business Analysts, Franchise Heads, Ecosystem Leads, and Solution Leads, as well as colleagues from Market Access, Medical, Commercial and Real-World Evidence. Together, you will support decision-making processes and contribute to patient-focused strategic priorities across multiple ecosystems.

What you will do

Support data-driven communication by preparing insights and enabling evidence-based discussions.
Translate business needs into short- to medium-term analytics solutions.
Contribute to dashboard and reporting automation (Power BI, Qlik).
Interpret and contextualize analytical results for business stakeholders.
Enable cross-functional collaboration across I2I, Medical, Access, and Commercial.
Assist in delivering training on dashboards and analytics solutions.

Interested? For this role we’re looking for:

MSc in Biotechnology, Economics, Medical/Biomedical Sciences, Business Chemistry, Health Economics or related fields.
Initial experience in analytics, performance management, or similar fields.
Strong communication interest and developing presentation skills.
Analytical mindset with problem-solving ability and business acumen.
Basic understanding of pharma go-to-market data preferred.
Foundational skills in Power BI and Excel with willingness to grow.
Excellent German language skills enabling confident, professional communication in a business environment, combined with very good English skills.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Sales Representative (m/f/d) for Osteoporosis (Monheim, Mettmann, DE)

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Within our Immunology Business Unit, we are looking for you to join our team as a

Sales Representative (m/f/d) for Osteoporosis

for the territory Stuttgart – Freiburg – Karlsruhe – Konstanz

About the Role

As a Sales Rep (m/f/d) for Osteoporosis, you will be responsible for building, developing, and maintaining customer relationships in your region, with a strong focus on discussing our innovative therapies in orthopedics and rheumatology.

Who You Will Work With & What You Will Do

You will have overall responsibility for the strategic and operational development of sales in your territory, working closely with colleagues from Sales, Market Access, and Medical.

What does this mean in practice?

You independently manage selected physician customers in line with the Omnichannel Cycle Plan (OCCP) and conduct sales discussions
You are responsible for providing scientific and product information regarding the use, effects, benefits, risks, and ingredients of the products, primarily to orthopedists and rheumatologists
You answer initial general customer inquiries in compliance with the product label
You identify new customers and regularly adapt the target group
You plan and conduct compliance-compliant events, including responsibility for territory-related budgets
You carry out monthly analyses of territory development and derive appropriate actions

Interested? For this position, we are looking for the following qualifications, experience, and skills

Certified pharmaceutical sales representative or a scientific/commercial qualification or a comparable qualification
At least 5 years of experience in pharmaceutical field sales, preferably in osteoporosis
Proven communication and sales skills
Experience in independently organizing and conducting medical events
Fluent in German, English at basic level
Willingness to travel and permanent residence within the territory

What We Offer

A high level of autonomy and a flexible, agile working environment
A culture where we achieve and celebrate success as a team
Top equipment (iPhone, laptop, company car, also available for private use)
The opportunity to make a meaningful contribution to improving medical care in the treatment of rheumatic diseases and osteoporosis
Freedom for personal development and the opportunity to actively shape your role
30+ days of vacation, attractive compensation, and flexible working hours
Corporate health management, sports programs, and pension benefits

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Analytical Critical Material Partner (Braine L'alleud, Walloon Brabant, BE)

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Nous recherchons un(e) Analytical Critical Material Partner analytique, rigoureux(se), proactif(ve) et collaboratif(ve) pour rejoindre notre équipe Global Analytical Operations, basée sur le campus UCB de Braine‑l’Alleud, Belgique.

À propos du rôle
Vous jouerez un rôle clé dans la sécurisation des approvisionnements en matières critiques pour les laboratoires analytiques, depuis la phase III jusqu’à l’ensemble du cycle de vie du produit. Vous veillerez à ce que les matières soient suivies, qualifiées, distribuées et conformes, tout en soutenant la qualité, la sécurité et l’amélioration continue. Votre travail soutiendra directement les laboratoires analytiques, les activités de fabrication et la chaîne d’approvisionnement à l’échelle mondiale.

Avec qui vous travaillerez
Vous travaillerez en étroite collaboration avec les laboratoires de contrôle qualité (QC) et de développement, les équipes Global Analytical Services, Manufacturing, Supply Chain et Qualité. Vous collaborerez à l’échelle mondiale avec des experts internes et des partenaires externes, afin d’assurer un flux de matières fluide et des opérations analytiques fiables au sein du réseau UCB.

Vos missions

Vous gérerez les stocks de matières critiques, incluant le suivi, les commandes, le stockage et la distribution via le LIMS.
Vous préparerez et aliquoterez les échantillons en toute sécurité sous hotte à flux laminaire (biosafety cabinet).
Vous coordonnerez les expéditions vers les laboratoires internes et externes et résoudrez les problématiques logistiques.
Vous assurerez le suivi des résultats de qualification, la gestion des certificats d’analyse (COA) et le support aux études de stabilité lorsque requis.
Vous contribuerez aux investigations de déviations, aux analyses de causes racines et au suivi des actions correctives.
Vous participerez aux projets d’amélioration continue et au renforcement de l’expertise LIMS.

Intéressé(e) ? Pour ce rôle, nous recherchons le profil suivant en termes de formation, d’expérience et de compétences :

Vous disposez d’une expérience en laboratoires analytiques, en environnement GMP ou dans des opérations réglementées.
Vous êtes à l’aise avec les systèmes LIMS et la gestion des données et de la documentation de laboratoire.
Vous faites preuve d’un grand sens du détail, de solides compétences organisationnelles et d’une forte autonomie dans votre travail quotidien.
Vous communiquez clairement et collaborez efficacement avec des équipes internationales et transverses.
Vous êtes proactif(ve), adaptable et motivé(e) par l’amélioration continue et la culture qualité.
Vous êtes à l’aise en lecture et en rédaction en anglais ; la maîtrise courante de l'anglais constitue un atout.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head of Integrated Planning and Performance (Slough, Berkshire, GB)

Make your mark for patients

We are looking for a Head of Integrated Planning and Performance who is strategic, collaborative, and forward-thinking to join our Integrated Program Management Office team, based in our Slough office, United Kingdom.

About the role

You will lead the development of unified planning and performance standards across our global Candidate and Asset programs, enabling teams to work with clarity, consistency, and data‑driven insights. You will drive the adoption of digital planning systems, strengthen performance monitoring practices, and ensure that teams across our research, development, manufacturing, and commercial functions can plan, monitor, learn, and adapt effectively. You will steer capability building in project management and lead a high‑performing team responsible for planning excellence and enterprise performance delivery.

Who you’ll work with

You will be working with a diverse global network of colleagues, partnering closely with Program and Project Management Teams across Candidate and Asset programs. You will also collaborate with Finance, Portfolio Management, Manufacturing, Commercial, Clinical and Data and Digital teams to ensure alignment and connectivity across planning cycles. Your team includes Project Managers and Planning and Performance specialists, all working together to deliver high‑quality plans executed with strong business performance.

What you’ll do

• Develop and govern enterprise planning standards, ensuring consistent planning practices across global teams.

• Maintain a unified planning data model and ensure planning information is accurate, connected, and reliable.

• Oversee performance monitoring cycles and deliver clear, actionable information to decision‑making bodies.

• Lead the development of project management capabilities, including training, methods, and best‑practice adoption.

• Build strong cross‑functional collaborations to ensure alignment across planning, governance, and performance cycles.

• Lead and mentor a team of planners and project managers, fostering growth, clarity, and effective delivery.

• Set the direction for digital adoption within the Integrated Program Management Team and coach the PMs on this journey.

Interested? For this role we’re looking for the following education, experience, and skills

• Post‑graduate degree in a relevant field; project management qualification preferred.

• Extensive experience in the biopharmaceutical sector with expertise in enterprise planning and performance management.

• Over 10 years’ experience in project or program management within complex, global environments.

• Strong knowledge of planning, scheduling, resource management, and performance analytics.

• Skilled in data interpretation, insight storytelling, and engaging communication with senior audiences.

• Proven leadership experience, with the ability to coach teams and drive capability development.

• Digital Fluency expected, with experience of using AI in Project Management

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technicien(ne) Biomanufacturing - Media & Buffer (Nuit) (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons plusieurs Technicien.nes Biomanufacturing – Media & Buffer (semaine shift de nuit) talentueux.ses et motivé.es pour rejoindre notre Belgium Biomanufacturing Operations Center à Braine-L’Alleud, Belgique.

Ici, vous pouvez réellement enrichir votre expertise dans un environnement dynamique et porteur, où votre épanouissement et votre développement sont prioritaires. En travaillant avec les technologies les plus récentes et des techniques inédites, vous contribuerez à produire des médicaments révolutionnaires pour apporter des améliorations réelles aux patients, aujourd’hui et à l’avenir.

Le rôle s’effectue à 100% sur site et comprend des horaires en shift, du dimanche au jeudi (22h-6h).

Concernant le rôle :

Vous contribuerez aux opérations de fabrication biotechnologique, de la préparation des milieux et tampons à la culture et purification des biomolécules, dans le respect des standards qualité, sécurité et réglementaires.

Vous travaillerez avec :

Vous intégrerez une équipe compétente et dynamique et interagirez quotidiennement avec l’ensemble des fonctions en charge du développement de notre nouvelle usine de production biotech.

Vos activités :

Réaliser les opérations de production conformément aux procédures
Mettre en service, surveiller et nettoyer les équipements
Ajuster les paramètres critiques du procédé
Produire des lots commerciaux en respectant les GMP (Good Manufacturing Practice)
Participer aux réunions opérationnelles et maintenir la zone de travail
Contribuer aux projets
Effectuer le nettoyage des locaux, la maintenance de premier niveau et les contrôles en cours de fabrication
Soutenir la réalisation des objectifs de l’équipe et assurer la coordination en cas d’absence du responsable
Identifier et signaler les risques liés à la sécurité, qualité ou délais
Initier des déviations qualité et participer aux audits internes/externes
Documenter rigoureusement les activités dans les systèmes
Respecter et promouvoir les bonnes pratiques de sécurité
Suivre le plan de formation et proposer des améliorations
Contribuer à l’amélioration continue et à l’intégration des nouveaux membres
Assurer la liaison avec les intervenants internes/externes pour les activités quotidiennes

Intéressé.e ? Pour ce poste, nous recherchons la formation, l’expérience et les compétences suivantes :

Expérience en production biotech ou pharma
Une précédente expérience en Media & Buffer est vivement souhaitée
Bonne connaissance des GMP (Good Manufacturing Practice)
Excellent esprit d’équipe et capacité à prendre des initiatives
Prise de décision et responsabilité à son niveau
Capacité à travailler dans un environnement dynamique et à gérer les urgences
Maitrise du français

#Biomanufacturing

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

MSL Rare Disease & Epilepsy Poland (Warsaw, Warsaw, PL)

Make your mark for patients

We are looking for a Medical Science Liaison Rare Disease & Epilepsy Poland to join us in our regional Medical Affairs team, field based in Warsaw, Poland.

About the role

As a Medical Science Liaison Rare Disease & Epilepsy Poland, you will identify and foster purposeful partnerships with key scientific influencers to drive new sources of patient value. The role it is field based.

What you’ll do

Agile and proactive identification and management of key scientific and medical influencers based on local ecosystem dynamics and stakeholder needs and drivers (from push to pull).
Exploration and identification of new sources of patient value (innovative solutions and services).
Manage and generate product/ disease state data (IIS, audits, RWE etc.).
Support clinical studies, clinical development and share insights with R&D team.
Serving as the leading local scientific expert for UCB solutions.
Supporting market access colleagues when applicable in presentation of RWE/HEOR/clinical information to regional and local payer accounts and formularies.

Interested? For this position you’ll need the following education, experience and skills:

Educational background: scientific profile preferred, university degree (Master, PhD) in Life Sciences, Medicine, Biology, Pharma.
Relevant therapeutic experience in neurology with minimum 2 years of MSL or pharmaceutical/healthcare industry related experience desired.
Effective communication and interpersonal skills including networking and presentation skills.
The ability to clearly articulate complex scientific in 1:1 and group settings.
Customer service oriented, business acumen required with the ability to take initiative and work both independently and in a team.
Willingness to travel extensively, both nationally and internationally, but also internationally (within the East Europe region). The position is field base (60%).
Languages: full professional proficiency in Polish and English (both oral and written).

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Business Analytics Lead TW/HK/SEA (Taipei, Taipei, TW)

Make your mark for patients

You will work as a dedicated Business Analyst Lead in close collaboration with Patient Impact Teams to enable data-driven decisions. Your key responsibilities include:

• Market & Insights: Develop a deep understanding of the local market and therapeutic areas (e.g., Rheumatology, Dermatology, Epilepsy, Lennox-Gastaut, Myasthenia Gravis); generate actionable insights and deliver analytics solutions to address key business questions.

• Launch & Strategy: Drive and support launch readiness strategies and project follow-up for new products and indications in collaboration with local teams and regional stakeholders, including the Intercontinental Analytics community.

• Performance & Forecasting: Manage performance through robust insights generation and support accurate forecasting, ensuring reliable projections to guide both strategic and operational decisions.

• Collaboration & Innovation: Partner with local and regional stakeholders to implement strategic imperatives and foster innovative business thinking through holistic, end-to-end analytics.

COMPETENCIES:

• MSc in Biotechnology, Economics, Financials or Medical related university degree

• Significant experience in consultancy, pharmaceuticals, or healthcare sector (+5-10 years)

• Excellent understanding of the pharmaceutical G2M data landscape

• Strong analytical and problem-solving skills with good business acumen

• Team player with the ability to work independently

• Excellent communication and stakeholder management skills

• Fast learner, curious and comfortable with ambiguity

• Fluent in Local Language & English (if different)

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Quality lead Chinese Mainland & Taiwan & HongKong (Shanghai, Shanghai, CN)

Make your mark for patients

We are looking for a Quality Lead to join us to lead Chinese Mainland, Taiwan and Hong Kong quality team, based in our Shanghai office.

About the role

This position Act as the primary Quality contact for the Affiliates in China and Taiwan/Hong Kong. Drive, oversee and manage the strategy and framework for Affiliate Market Quality activities.
Direct oversight to Affiliate quality personnel in Chinese mainland and Taiwan/Hong Kong.

Foster a culture of collaboration and continuous improvement, emphasizing oversight to implementation and compliance to UCB quality standards, policies, procedures, including compliance of cGxP regulation(s) imposed on controlled or un-licensed medicinal products by national laws or applicable regulatory authorities.
Assist in the identification and mitigation of GMP/GSP quality issues and risks, highlight or facilitate improvement opportunities or solutions.
Work with stakeholders (e.g., Affiliate Management, Market Quality, Global Quality, Supply Chain, Pharmacovigilance, Regulatory) organizations to facilitate support for the local Quality organization and ensure GxP operations deliverables are achieved in a timely manner.
Support the Market Quality organization, using UCB procedures and guidelines, when identifying the right talents and appropriate resources to achieve compliance, in line with UCBs vision and values.
Have overall accountability for the Quality Responsible Person (QRP) function related to the China affiliate Drug Distribution License (GSP), ensuring effective oversight and appropriate support to enable the designated QRP to exercise decision‑making authority over quality management in accordance with regulatory requirements. Where required, personally assume QRP responsibilities.

What you’ll do

Apply for and maintain the China affiliate Drug Distribution License (GSP) through appropriate oversight and governance. When required, personally assume and perform the role and responsibilities of the Quality Responsible Person (QRP) in accordance with applicable GSP regulations.
Ensure that the required QMS for the Domestic Responsible Entity (MAH deputy) is established and effectively implemented in accordance with local laws and regulations, including the preparation of required documents such as the China Annual Report.
Ensure oversight and execution of the local Quality Management System:
Provide subject matter expertise and represent department interests in meetings, projects, committees, and improvement initiatives, as requested.
Ensure compliance to applicable data integrity standards and procedures.
Take role as Taiwan and Hong Kong Affiliates backup QA for batch release and complaint handling operation as needed.
Act as Bio-safety responsible person to ensure required CIQ essential process & biosafety manual in place and in use
Act as Document controller for Chinese affiliate in UCB eQMS

Interested? For this role we’re looking for the following education, experience and skills

Bachelor’s degree and above; Pharmacist License is preferred
10+ years’ Quality experience within regulated pharmaceutical environment. Consumer Healthcare or Pharma industry preferred.
Strong knowledge of China MAH/GMP/GSP regulatory compliance, including experience with regulatory audits and inspections.
Should be a self-motivated team player that is able to work autonomously, exercise good judgement, using a quality mindset, ability to handle complex/difficult situations, foster an attitude of collaboration, and ability to act as a role model for others in driving the company vision, incorporating strong ethical and patient focused principles.
Experience operating in a multi-cultural and locational environment. Must be able to effectively interact and communicate (verbally and written) with internal and external stakeholders. Ability to communicate both verbally and in writing using the local country language, and English is preferred.
Experience in people management, including oversight to day-to-day responsibilities, performance monitoring, and providing guidance on career growth and development.
Experience in developing effective solutions that foster process and business improvement.
Experience in Pharmaceutical manufacturing site is an advantage
Experience in project management, quality auditing, risk management, and data analytics is preferred.
Experience using key computerized systems (e.g., SAP, Veeva, Microsoft applications).
Ability to travel when required.
Fluent Chinese and working‑level English proficiency required to effectively execute job responsibilities.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Statistician (Shanghai, Shanghai, CN)

Make your mark for patients

We are looking for a Statistician to join us in our Biometrics and Data Science team, based in our Shanghai office

What you’ll do

Can provide direction of the biometrics (statistics) team at the study level, or a biometrics (statistics) team in a specific area (e.g., safety, launch, pre-clinical) in aspects of trial level design, analysis or reporting
Contributes to and influences the translation of strategy to tactical planning, operations, and quality
Expected to work closely with the PLS to support in providing guidance in the overall strategy to the Development and Regulatory leads
Aides in reviewing and producing deliverables from the biometrics (statistics) team to the larger study team
Contributes to the continuous learning and upskilling culture for a modern Biometrics (Statistics) organization
Supports the transformation of the statistics operating model
Work closely with peers across BDS, implement the UCB Data Strategy, and critical business functional areas to ensure functional excellence and collaboration
Operates as a change ambassador
Study accountability leading to high quality internal decision making and external stakeholders

Interested? For this role we’re looking for the following education, experience and skills

Master’s Degree (preferred) in Biostatistics or Statistics or Bachelors (with relevant experience)
Entry level for Master’s degree with prior experience in a placement/internship with a pharma/biotech
Basic knowledge of drug development across all phases
Influencer and collaborator
Acts with a measured sense of urgency
Experience in communicating complex quantitative ideas clearly with all levels of technical and non-technical personnel, in local and international environments
Has the ability to translate ideas and inferences to non-experts
Proficient in a statistical programming language (e.g., SAS or R) and sample size and simulation software (e.g., EAST, nQuery, WinBugs, etc)
Basic experience with designing, analyzing, and reporting Phase I-IIIB clinical trials; can be in an academic setting.
Basic knowledge of Drug Development and SDTM/ADaM CDISC standards

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Computerized Systems Quality Assurance - ERP (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

To strengthen our GxP Compliance (Data Integrity and Digital Compliance) department, we are looking for a talented profile to fill the position of: Computerized Systems Quality Assurance (CSQA) - ERP, Braine l’Alleud, Belgium

About the role

The CSQA Specialist is responsible for ensuring that all GPvP/GCP/GLP relevant computerized systems across the organization are validated, compliant, and maintained according to regulatory requirements and industry best practices. This role provides expert guidance on CSV/CSA, data integrity, system lifecycle management and quality oversight of digital and automation initiatives within a pharmaceutical environment.

You will work with

You will work closely with the Head of GxP Data Integrity & Digital Compliance, Data Office, IT, Knowledge Management, and other key stakeholders. This role requires you to collaborate with cross-functional teams to address and mitigate data integrity risks and drive continuous improvement within UCB.

What you will do

Quality Oversight & Compliance

Provide senior‑level QA oversight for the full lifecycle of GxP computerized systems (from concept to retirement).
Ensure compliance with global health authority expectations (FDA, EMA, MHRA), industry standards (GAMP 5, ICH Q9/Q10), and data integrity principles (ALCOA+).
Review and approve validation deliverables such as validation plans, risk assessments, design, data integrity risk analysis, test strategies, test cases and validation reports.
Ensure adherence to internal policies, SOPs, and quality standards for computerized systems.

CSV/CSA Leadership

Lead and support Computerized System Validation (CSV) and Computer Software Assurance (CSA) activities using a risk-based approach.
Drive adoption of CSA principles to optimize and streamline validation effort while ensuring compliance.
Contribute to the development and continuous improvement of CSV/CSA frameworks, templates, and procedures.

Project & Stakeholder Management

Provide QA guidance to project teams during system implementation, upgrades, integrations, and migrations.
Partner with IT, QA, Patient Safety, Clinical, R&D, and Automation teams.
Facilitate cross-functional decision-making and serve as a key QA representative in system-related projects.

Vendor & Audit Management

Perform supplier qualification audits and quality assessments of technology partners.
Ensure that third‑party service providers and Software-as-a-Service (SaaS) systems meet regulatory and contractual requirements.
Support internal audits and external regulatory inspections (e.g., FDA, EMA).
Develop vendor assessment process and governance.

Data Integrity

Lead data integrity reviews, risk assessments, and remediation plans, maturity assessment
Provide expert guidance on secure data handling, audit trail review, user access management, and data governance.

Deviation & Change Management

Review and approve deviations, CAPAs, and change controls for GxP systems.
Conduct impact assessments and ensure effective CAPA implementation.

Training, Coaching & Continuous Improvement

Train teams on CSV/CSA principles, data integrity, and GxP requirements.
Mentor junior CSQA/CSV staff and support capability building across the organization.

Interested? For this position you’ll need the following education, experience and skills

Bachelor’s, master’s degree or an education in a relevant scientific discipline
Fluent English communication (oral and written); any additional languages are a plus.
A minimum of 5 to 10 years of progressive experience in the pharmaceutical industry within Quality Assurance
Solid experience with ERP systems in a CSV‑regulated QA environment
Robust and hands‑on expertise in Computer System Validation (CSV), including validation planning, execution, documentation oversight
Significant exposure to pre‑clinical, clinical, and post‑market environments is strongly preferred
A good and thorough understanding of current regulatory requirements and expectations (e.g., US, Europe, Japan, China) and an ability to interpret current regulations and requirements is essential
Experience in managing various GxP Inspections across geographies, including inspector facing experience
Should possess outstanding presentation abilities and be capable of delivering content persuasively and effectively to senior management.
Negotiation skills and a proven ability to influence senior leaders and others within a global matrix organization
Must be knowledgeable of risk analysis techniques (FMEA, …), must be able to identify and evaluate risks and propose mitigation plans within complex situations
Demonstrates the ability to recognize and address critical issues, with escalation to executive management as necessary

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Global Logistics Operations LKU Expert (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Global Logistics Operations Local Key User who is analytical, collaborative, and impactdriven to join our Global Logistics Operations (GLO) team, based at our UCB campus located in Brainel’Alleud, Belgium..

About the role:

You are going to play a pivotal role in shaping, optimizing, and sustaining global logistics processes across our operational network. You will combine deep logistics expertise with system and process know-how to strengthen governance, improve performance, and support longterm transformation initiatives. Beyond daily operations, you will influence strategic decisions and help build futureready logistics capabilities across Global Supply Chain.

Who you will work with:

You will work closely with Global Logistics Operations teams, business solution experts, and IT partners within the Global Supply Chain organization. You are going to collaborate across functions such as quality, procurement, customer operations, and external partners, contributing to a strong center of excellence culture focused on collaboration, continuous improvement, and knowledge sharing.

What you will do :

You will Lead Global Logistics Operations process harmonization & improvements across affiliates, partners, and internal flows.

You will act as a subject matter expert for logistics processes, SAP flows, and transformation initiatives.

You will govern logistics SOPs and ensure compliance, consistency, and operational excellence.

You will develop and deliver trainings to strengthen process and system capabilities globally.

You will manage logistics master data governance to ensure data quality and global standards.

You will provide functional and operational guidance within GLO.

Interested? For this role, we are looking for the following education, experience, and skills:

Bachelor’s or Master’s degree in supply chain, logistics, or a related field.

Minimum 5 years’ experience in logistics operations or supply chain environments.

At least 3 years’ handson experience with SAP logistics modules (SD Mandatory , WM or EWM).

Strong analytical mindset with proven experience in process optimization.

Excellent stakeholder management and communication skills in English, French is considered an asset.

Experience in cross-functional projects or transformation initiatives is an asset

Experience in managing or coaching a team is a plus

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Process Engineer (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Process Engineer who is collaborative, solution‑oriented, and quality‑driven to join our Sterile Process Engineering team, based at our UCB campus located in Braine‑l’Alleud, Belgium.

About the role
You are going to play a key role in shaping the future of sterile manufacturing at UCB. As a Process Engineer, you will act as the user representative and project leader for digital and non‑digital initiatives impacting the Sterile Manufacturing Plant. You will drive projects from feasibility to deployment, ensure compliance with GMP and data integrity requirements, and support production teams with strong technical and IT expertise.

Who you will work with
You will work closely with a multidisciplinary network including Production, Engineering, Quality, IT and HSE. You are going to collaborate daily with suppliers, internal experts, project teams, and stakeholders across UCB, contributing to a shared vision of operational excellence, compliance, and continuous improvement within a highly matrixed environment.

What you will do

You will lead or support sterile manufacturing projects from feasibility, risk analysis, and execution to operational handover.
You will lead digitalization initiatives impacting sterile manufacturing in Braine.
You will write, review, and approve GMP documentation supporting production, validation, and regulatory submissions.
You will ensure data integrity, cybersecurity compliance, and 21 CFR Part 11 alignment across departmental activities.
You will provide first‑line IT and process support to production teams, investigations, deviations, and CAPA.
You will drive continuous improvement, technology watch, and contribute to a safer, greener manufacturing environment.

Interested?

For this role, we are looking for the following education, experience, and skills:

You hold a Master’s degree in Engineering, Pharmacy, IT, or equivalent relevant experience.
You bring strong knowledge of GMP requirements and sterile manufacturing environments.
You are experienced in project management and cross‑functional coordination.
You have a very good command of both French and English
You can translate operational needs into IT solutions and IT concepts into manufacturing reality.
You are autonomous, rigorous, and comfortable working in a dynamic, matrixed environment.
You demonstrate strong communication skills, a collaborative mindset, and a proactive approach to problem‑solving.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Patient Supply Data Product Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Data Lead who is analytical, collaborative, and highly organized to join our Digital Transformation Team, based at our UCB campus located in Braine‑l’Alleud, Wallonia, Belgium.

About the role:

In this role, you are going to ensure that data across Patient Supply is accessible, reliable, and seamlessly integrated. You will manage the lifecycle of data integrations, support validation activities, and align system configurations with business priorities. You will work closely with data experts, IT teams, and business stakeholders to build a strong, future‑ready data environment. Your work will directly support UCB’s digital initiatives and strengthen the governance and quality of critical data assets.

Who you will work with:

You will collaborate with the Data Integration Lead, Data Architect, Data Governance Manager, Data Innovation Lead, IT teams, and business stakeholders across Patient Supply. You will act as a key connector between technical and business teams, ensuring that integration activities run smoothly, data standards are respected, and system validation meets regulatory expectations. You will be part of the Data Strategy Team, supporting digital transformation and enabling data‑driven decision‑making.

What you will do:

You will manage and prioritize business requests and oversee incident, change, and access tickets.
You will be responsible for ensuring procedures, documentation, and data integrations meet UCB data quality standards.
You will collaborate with Data Integration and Governance teams on changes impacting data rules and processes.
You will execute validation activities, test scripts, and ensure compliance of system configurations.
You will coordinate integration needs linked to new or upgraded systems across all departments involved.
You will support audits by providing validation evidence and ensuring adherence to data integrity requirements.

Interested? For this role, we are looking for the following education, experience, and skills:

Bachelor’s or Master’s degree; SQL, Power BI, or other relevant certifications are a plus.
1–2 years of experience in data management and 1–2 years in practical programming.
2–3 years of experience in the pharma or biopharma sector.
Strong knowledge of databases, ETL/ELT logic, SQL, data modeling, and data transformation.
Experience with tools such as Collibra, Power BI/Fabric, Snowflake, Oracle SQL, HPALM, and DMS.
Excellent communication skills, strong organization, autonomy, analytical thinking, and
Full fluency in English and French.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head of Quality Systems & Continuous Improvement (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Head of Quality Assurance Compliance who is strategic, collaborative, and relentlessly quality-driven to join our Site Quality – QA Compliance team, based at our UCB campus located in Braine-l’Alleud, Walloon Brabant, Belgium.

About the role

You are going to set the pace for regulatory compliance and inspection readiness across our pharmaceutical manufacturing site. You will lead the site Quality Management System governance, strengthen a proactive and risk-based compliance approach, and champion a culture where quality is everyone’s responsibility. You will oversee key compliance processes—audits, deviations, corrective and preventive actions, change control, data integrity, and risk management—so you will help protect patients, products, and reliable supply.

Who you will work with

You will work closely with the Site Quality leadership and partner daily with Manufacturing, Technical Operations, Regulatory Affairs, and global Quality colleagues to keep the site in a sustained state of control. You will also collaborate with quality systems and continuous improvement experts who focus on optimizing quality processes, reinforcing standards, and enabling operational excellence across site activities and supporting services.

What you will do

• You will drive inspection readiness and sustained compliance across manufacturing, testing, and all supporting site services.
• You will lead Quality Management System governance, ensuring robust oversight of deviations, corrective actions, and change control.
• You will coordinate regulatory and customer inspections, including preparation, hosting, and timely, high-quality response packages.
• You will lead internal and external audit strategy, ensuring effective follow-up, risk mitigation, and continuous improvement outcomes.
• You will manage the site data integrity office, define the roadmap, and strengthen oversight for equipment-related data.
• You will build, coach, and inspire a high-performing compliance team and develop a practical learning and training culture.

… Interested?
For this role, we are looking for the following education, experience, and skills:
• You will bring a Master’s degree in Chemistry, Life Sciences, or a closely related scientific discipline.
• You will have 10+ years in a regulated pharmaceutical or life-sciences environment, including 5+ years in Quality Assurance.
• You will demonstrate strong people leadership experience, motivating and developing teams of quality professionals.
• You will show expertise in quality systems governance and internal/external auditing within manufacturing environments.
• You will apply risk analysis and mitigation methods with confidence and sound, fact-based decision making.
• You will communicate fluently in French and English, influencing stakeholders with clarity, diplomacy, and accountability.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Artwork & Packaging Development Expert (Belgium) (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

About the Role

Who You’ll Work With

What You’ll Do

Within the Artwork & Packaging Program governance structure, you contribute with expert authority, among peer experts, with accountability for high‑quality development deliverables and activities (while Program Leads act as the central SPOC for cross‑functional oversight).
Lead secondary and tertiary packaging development projects from early concept to commercial launch through design validation, visual identity activities and industrialisation support. Clinical Trials packaging is part of the scope.
Drive development of innovative, manufacturable, and cost-effective packaging solutions that create patient, stakeholders and brand value.
Drive creation, evolution, and governance of visual identity, graphic charters, and artwork deliverables.
Ensure development processes, SOPs, and training materials are in place, followed, and continuously improved.
Identify packaging features that support patient usability, compliance, manufacturing efficiency, and supply chain reliability, cost consciousness
Support lifecycle optimisation initiatives, including cost of goods (COGs) improvement and packaging standardisation.
Provide technical expertise to packaging sites and partners, supporting troubleshooting, capacity optimisation, and technology transfer.
Understanding printing techniques and underlying impacts-constraints on branding-packaging development.
Contribute to the development and implementation of global packaging standards, guidelines, and design platforms and technical features.
Monitor external trends, technologies, regulations, and standards related to packaging and artwork, ensuring timely adoption and communication.
Support long-range manufacturing and packaging strategies, including risk assessment and mitigation planning.

Interested? For this role we’re looking for:

Strong communication skills with the ability to engage diverse technical and non-technical stakeholders.
Proactive, pragmatic, and solution-oriented working style, with the ability to manage multiple priorities.
Ability to influence, lead, and deliver results without direct authority.
Business proficiency in English.
Bachelor's or master's degree in engineering, packaging science, life sciences, or a related discipline.
5–10 years’ experience in packaging development within a GMP regulated pharmaceutical environment.
Solid project management experience in global, cross functional environments.
Demonstrated understanding of development activities related to secondary-tertiary packaging within manufacturing network across the end-to-end from clinical, human factors usability studies, submission into commercial launch and later lifecycle.
Strong knowledge of graphic design, visual identity creation, and regulatory labelling requirements.
Sustainability knowledge skills (understanding of materials, processes, and design strategies that minimize environmental impact, reduce waste, and promote recyclability and efficient use of resources).
Experience managing artwork development and external partners (design agencies, CMOs) is a strong advantage.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

QA Manager - QC Process Support (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

To strengthen our Global QA for QA Operations department we are looking for a talented profile to fill the position of: QA Manager – QC Process Support – Braine l’Alleud, Belgium.

About the role

The QA Manager – QC process support provides quality expertise and ensures appropriate global oversight of Patient Supply Quality Control processes, with a primary focus on the execution of QC processes and related projects, including specifications, stability studies (protocols and reports), analytical reference standards, critical materials and standards, laboratory third parties, compendial changes and raw‑material vendor certification.

You will work with

The QA Manager – QC process support works closely with Patient Supply Quality Control teams, relevant supporting functions, and external laboratory partners and Contract Laboratory Organizations (CLOs). The role collaborates cross‑functionally to ensure compliant execution of global QC activities, effective management of QC processes such as management of critical materials and stability studies, and smooth coordination between QC, supporting services, and external partners.

What you will do

Back-up Function

The position can act as back-up for his direct colleagues or for his manager according to the manager’s instructions and after appropriate training

General QA Role

Using a Risk Based Approach, ensure that PSQC Processes & Operations are compliant with applicable regulations and guidelines (EMEA, FDA, PIC/S, ICH, best practices as defined by relevant organizations) and UCB Policies & Procedures
Drive quality leadership and provide technical expertise on compliance strategy.
Communicate processes requirements effectively across functional areas.
Promoting culture of quality, operational excellence and “SOSD” (See it, Own it, Solve it, Do it) attitude within Patient Supply Quality Control.
Deliver general cGMP training and effective coaching on QMS to relevant stakeholders.
Communicate compliance status and issues to appropriate organizational levels.
Support regulatory inspections/audits, providing dynamic assistance to SME’s.

Patient Supply Quality Control Process

- Participate in the improvement of the PSQC processes
- Ensure adequate coaching and training of relevant stakeholders on the PSQC processes
- Oversee critical global activities to ensure analytical operations are conducted in accordance with UCB Quality Standards and applicable national and/or international regulations and guidelines (EMEA, FDA, PIC/S, ICH)
- Ensure subcontractors supporting QC routine operations maintain adequate cGMP standards
- Implement and maintain adequate Quality & Compliance indicators and communicate results to appropriate levels of the organization

Continuous Improvement

- Identify, coordinate and support opportunities for improvement and operational excellence projects in response to business needs, technical changes, risks, audit observations and regulatory requirements.
- Lead or co-lead internal quality spot checks/audits to ensure compliance with internal standards and worldwide regulatory requirements with respect to cGMP.
- Conduct or support Quality Reviews exercises (e.g. Management/Product Reviews, etc)
- Identify, coordinate and support Continuous Improvement projects (LEAN, 6-Sigma, Green belt and others) with QC management to enhance quality KPI’s and product/process quality.

Interested? For this position you’ll need the following education, experience and skills

Bachelor’s, master’s degree or an education in a relevant scientific discipline
Fluent English & French communication (oral and written)
Strong knowledge and proven experience in Quality Control and applicable regulations
Proven understanding of QC processes: stability studies, material management, specification management.
Experience with Quality Management System and Internal/External Auditing
Ability to balance multiple priorities, provide leadership and prioritisation, and work with minimal supervision
Fact based decision maker with accountability and delivering attitude
Excellent team player attitude with excellent interpersonal relationship and communication skills
Ability to plan and direct the actions of a group of professionals and Quality Assurance personnel in multidisciplinary investigations / meetings
Able to perform effectively in high‑pressure situations

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Patient Supply Data Architect Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Patient Supply Data Architecture Lead who is strategic, decisive, and collaborative to join our Patient Supply Digital Transformation team, based at our UCB campus in Braine‑l’Alleud, Belgium.

About the role:

In this role, you will shape the future of Patient Supply data at UCB. You will define, govern, and evolve the end‑to‑end data architecture that underpins analytics, automation, and AI at scale. You are going to act as the architectural authority, ensuring data products are coherent, scalable, compliant, and future‑proof. You will balance immediate delivery needs with long‑term sustainability, enabling trusted insights across domains in a highly regulated environment.

Who you will work with:

You will work closely with Data Product Leads, Data Governance, Analytics and AI Product Leads, and Digital Technology teams within the Data Foundations Hub. You are going to collaborate across Patient Supply transformation initiatives, acting as a trusted architecture advisor and enabling alignment across domains in a global, matrix organization.

What you will do :

You will define, own, and evolve the end‑to‑end Patient Supply data architecture.
You will own the unified data model and ensure consistency across domains and data products.
You will act as final authority on data modelling and architectural design decisions.
You will ensure data products are analytics‑ and AI‑ready by design.
You will embed compliance, traceability, and auditability into data architecture.
You will guide teams to prevent fragmentation and promote architectural reuse.

Interested? For this role, we are looking for the following education, experience, and skills:

Bachelor’s or Master’s degree in a relevant field.
Deep experience in data architecture and enterprise‑scale data modelling.
Proven experience in GxP‑regulated pharmaceutical or life sciences environments.
Strong understanding of data integrity, compliance, and traceability principles.
Ability to influence and align stakeholders without formal authority.
Excellent communication skills with both technical and non‑technical audiences.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Manufacturing Data Owner (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Manufacturing Data Owner who is analytical, accountable, and collaborative to join our Patient Supply Data & Governance team, based at our UCB campus in Braine-l’Alleud, Belgium.

About the role:

In this role, you will translate data strategy into operational reality. You will own manufacturing data end-to-end, ensuring it supports business decisions, operational performance, and regulatory compliance. You will define how data is created, governed, used, and protected across systems and processes. Acting as the single point of accountability, you will drive consistent data governance while empowering teams to manage data quality day to day.

Who you will work with:

You will work closely with Data Stewards, Process Owners, IT System Owners, and the Data Governance Core Team within Patient Supply. You will collaborate across manufacturing, quality, and supply chain teams, acting as a bridge between business, data, and regulatory requirements at both local and global levels.

What you will do :

You will own manufacturing data end-to-end, from definition to lifecycle management.
You will define business rules, data definitions, quality thresholds, and usage conditions.
You will set data quality standards and decide on corrective and preventive actions.
You will assess data impacts of system, process, and structural changes.
You will ensure data governance policies are consistently applied across Patient Supply.
You will lead data governance initiatives to improve harmonization and interoperability.

Interested? For this role, we are looking for the following education, experience, and skills:

Bachelor’s or Master’s degree in a relevant field.
Experience in data management and data governance foundations.
Strong background in GMP/GDP quality systems within regulated environments.
Solid understanding of GxP regulations and pharmaceutical product lifecycle.
High data literacy with strong analytical and organizational skills.
Fluent in English and French, with clear stakeholder communication ability.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technicien(ne) Upstream Biomanufacturing - Nuit (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons plusieurs Technicien.nes Biomanufacturing Upstream (semaine shift de nuit) talentueux.ses et motivé.es pour rejoindre notre Belgium Biomanufacturing Operations Center à Braine-L’Alleud, Belgique.

Le rôle s’effectue à 100% sur site et comprend des horaires en shift, du dimanche soir au vendredi matin (22h>6h).

Concernant le rôle :

Cette fonction est l’opportunité de participer activement aux activités de mise en place des zones de production de notre nouveau bâtiment Biotech.

Vous travaillerez avec :

Vous intégrerez une équipe compétente et dynamique de technicien.nes de production et interagirez quotidiennement avec l’ensemble des fonctions en charge du développement de notre nouvelle usine de production biotech.

Vos activités :

Réaliser, mesurer, analyser, suivre et ajuster les activités liées aux processus Upstream
Assurer l’exactitude de la traçabilité des tâches effectuées
Participer à la mise en place des zones de production et aux activités nécessaires pour le démarrage de la production
Effectuer les lots de productions techniques, de validations et de productions continues selon les procédures établies
Identifier les risques potentiels lors de l’exécution des activités (santé, sécurité et environnement, qualité, coût, timing, etc.) et les reporter aux responsables
Participer à l’intégration et au coaching des nouveaux venus sur le projet

Intéressé.e ? Pour ce poste, vous devez posséder la formation, l’expérience et les compétences suivantes :

Bachelier en Biologie / Biochimie / Biotechnologie ou équivalent par expérience
Minium 1 an d’expérience dans le domaine de la production biotech / pharma en milieu GMP (Good Manufacturing Practices)
Une précédente expérience réussie en Upstream est vivement souhaitée
Capacité à gérer des situations urgentes
Bonne connaissance des systèmes automatisés
Désireux.se de travailler dans un environnement high-tech
Maitrise du français

#Biomanufacturing

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Technicien(ne) Upstream Biomanufacturing - Nuit (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Le rôle s’effectue à 100% sur site et comprend des horaires en shift, du dimanche soir au vendredi matin (22h>6h).

Concernant le rôle :

Cette fonction est l’opportunité de participer activement aux activités de mise en place des zones de production de notre nouveau bâtiment Biotech.

Vous travaillerez avec :

Vos activités :

Réaliser, mesurer, analyser, suivre et ajuster les activités liées aux processus Upstream
Assurer l’exactitude de la traçabilité des tâches effectuées
Participer à la mise en place des zones de production et aux activités nécessaires pour le démarrage de la production
Effectuer les lots de productions techniques, de validations et de productions continues selon les procédures établies
Identifier les risques potentiels lors de l’exécution des activités (santé, sécurité et environnement, qualité, coût, timing, etc.) et les reporter aux responsables
Participer à l’intégration et au coaching des nouveaux venus sur le projet

Intéressé.e ? Pour ce poste, vous devez posséder la formation, l’expérience et les compétences suivantes :

Bachelier en Biologie / Biochimie / Biotechnologie ou équivalent par expérience
Minium 1 an d’expérience dans le domaine de la production biotech / pharma en milieu GMP (Good Manufacturing Practices)
Une précédente expérience réussie en Upstream est vivement souhaitée
Capacité à gérer des situations urgentes
Bonne connaissance des systèmes automatisés
Désireux.se de travailler dans un environnement high-tech
Maitrise du français

#Biomanufacturing

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

External Manufacturing Operations Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for an External Manufacturing Operations Lead to join us in our External Manufacturing Department, based in Braine, Belgium.

About the role

Who you’ll work with

What you’ll do

Support reliability, robust processes, prompt issue resolution, and strong partnerships with vendors and internal stakeholders
Guide third parties vendor teams, coordinating cross-functional and inter-company activities
Participate in projects to foster operational excellence within UCB external manufacturing
Maintain governance structures and facilitate regular meetings between CMOs and UCB teams
Conduct operational performance evaluations and management processes for third parties
Provide operational expertise to support effective processes and optimized capacity utilization
Lead troubleshooting and investigations in collaboration with third parties, coordinating corrective actions
Identify and deliver continuous improvement projects to enhance quality, cycle times, and cost efficiency
Ensure compliance with regulatory standards and industry regulations
Prepare business and operations plans, defining operational management based on commercial strategy
Manage risks, including capacity availability and potential supply chain disruptions
Monitor third parties capacities and implement long-range product plans
Share technology knowledge, market intelligence, and product knowledge

Interested? For this role we’re looking for the following education, experience and skills

Master’s degree or PhD in life sciences with at least 7 years of relevant experience
Knowledgeable in technical and manufacturing aspects related to the portfolio area
Ability to lead multi-functional teams, motivate others, ensure responsibility, and focus on goals
Skilled in managing external business partners and relationships
Basic knowledge in financial and business knowledge. Capable of developing and analyzing business cases
Able to clarify complex technical and manufacturing performance issues
Capable of summarizing and presenting scenarios to support decision-making
Experience in crisis management and related communication
Strong problem-solving, project management and strategic thinking
Experience in operational excellence is a plus
Fluent in English (written and spoken), French is a plus

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Clinical Supply QP Partner (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

To strengthen our Clinical Supply Quality department we are looking for a talented profile to fill the position of: Clinical Supply QP Partner - Braine l’Alleud, Belgium.

About the role

As Qualified Person for IMP batch release, the Clinical Supply QP Partner acts as QP according to current regulation for Investigational Medicinal Products and is responsible for the management of batch disposition and release activities concerning the provision of IMP for UCB sponsored Clinical Trials. You will also act as Responsible Person, as per definition in the Good Distribution Practices.

As a member of the Clinical Supply Quality team, as Clinical Supply QP Partner you will responsible for, but not limited to the review of IMP batch records, ensuring the prompt resolution of all batch manufacturing issues and ensuring close out of development related CAPAs. This role provides direct partner driven, pragmatic and proactive support for development manufacturing.

You will work with

In this role, you will collaborate closely with the Clinical Supply Chain team, acting as the primary Quality Assurance liaison to ensure alignment and compliance across activities. You will also work in partnership with Regulatory Affairs to support regulatory requirements and submissions, while maintaining strong and continuous interaction with other Quality Assurance teams to ensure consistency, knowledge sharing, and best

What you will do

Operational

Ensure the manufacture, certification and distribution of Investigational Medicinal Products, is according to:

EC GMP guidelines (EudraLex - The Rules Governing Medicinal Products in the European Union, volume 4 – last edition)
Clinical Trials Regulation EU No 536/2014 and associated documents
Principe of Good Distribution Practices as required in EC Directive 2013/C68/01

Provide timely and efficient GMP/GDP IMP Release function to all relevant UCB project activities related to the development of the pipeline projects (included all relevant activities for IMP release: batch record documentation, etc…).
Support compliance with all relevant and appropriate regulations and guidelines, such as those relating to GMP/GDP, health and safety, etc.
Support in-licensing activities by providing Quality Assurance expertise for the evaluation of new project opportunities including participation in due diligence activities.
Ensure the Clinical Supply Quality activities are consistent across the range of different environments and teams supported (Vendors / Suppliers / in house).
Proactively support the activities of Clinical supply for relevant manufacturing quality systems (deviation close out / Change management / complaints / quality improvement).
Identify and facilitate resolution of technical and manufacturing quality issues that may impact the quality of the CMC sections of regulatory submissions.
Provide support in the evaluation of Temperature excursions for IMP.
Contribute the preparation of audits (internal/external, regulatory inspections)
Lead internal audits / Self-Inspections

Process

Ensure that all review and release, manufacturing and packaging operations are appropriately compliant with applicable regulations (EMEA, FDA, DEA, MHRA, etc. where relevant). Support the Head of Clinical Supply Quality in ensuring an acceptable outcome of all audits and inspections, especially those by government agencies, as they pertain to Process Support and Package Development practices (where relevant), equipment, and facilities.
Actively participate in identifying, developing and implementing local quality and operational excellence improvements in response to business requirements, technical changes and regulatory requirements by encouraging others to seek opportunities for different and innovative approaches to addressing problems and developing solutions.
Ensure Clinical supply Quality processes directly support Technical Operations and development partner goals and objectives.
Review and QA approval of deviations, change controls and complaints.

Interested? For this position you’ll need the following education, experience and skills

Bachelor’s, master’s degree or an education in a relevant scientific discipline
Fluent English communication (oral and written); any additional languages are a plus.

Qualified Person (QP) Belgium number
Good knowledge of cGMP and relevant regulatory requirements (e.g US, European, Japanese)
At least 5 years’ experience in QA/compliance experience in pharmaceutical regulated environment
Function effectively with minimal supervision
Good teamwork and project management skills. Must have strong, organization and analytical skills.
Fact based decision maker: understand complex issues and have the ability to contribute to informed decision making when working on “grey” issues
Able to make/influence quality/compliance decisions in a CMC development environment.
Experience of participation in failure investigations
Familiarity with risk analysis techniques

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

MSAT Investigation Lab Technician (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for an Analytical Laboratory Technician, who is curious, rigorous, and collaborative, to join our Bio Manufacturing Sciences & Technology (MSAT) investigation lab & data team, based in Braine‑l’Alleud, Belgium.

About the role

You will perform analytical testing that supports late‑stage and commercial biologic medicines. Your work will include applying and transferring analytical methods into the laboratory, supporting process transfer and validation, verifying data quality, and in some cases evaluating new technologies. You will deliver accurate, reliable results to agreed timelines while working on approved procedures, quality standards and health, safety, and environmental requirements.

Who you’ll work with

You will join the analytical sub-team of the Bio MSAT Investigation lab team. Day‑to‑day, you will collaborate with peers who run analyses, review and release results, maintain equipment readiness, and contribute to investigations and continuous improvement across the laboratory. You will also collaborate with colleagues from In-process Analytical Sciences and Analytical Development departments, Manufacturing and Quality.

What you’ll do

Conduct analytical testing using equipment such as liquid chromatography and capillary electrophoresis, ensuring compliant documentation within electronic laboratory notebook.
Set up and transfer analytical methods into the laboratory.
Verify results through peer review to ensure accuracy and reliability.
Support process transfers and validations for late‑stage and commercial biologics by providing analytical testing and documentation.
Report out-of-specification or out-of-trend results, participate to root-cause analysis investigations to propose and implement preventive and/or corrective actions.
Maintain equipment and facilities; ensure calibration, preventive maintenance, and safe operations
Handle laboratory samples and consumable reception and inventory, ensuring traceability.
Propose improvements to methods, workflows, and training.

Interested?

For this role we’re looking for the following education, experience and skills

Bachelor’s in chemistry, biochemistry, biotechnology, or related field.
Two or more years in a quality‑focused laboratory performing analytical testing for biologics or comparable complex molecules.
Hands‑on experience with liquid chromatography and capillary electrophoresis is a must. Other techniques applied to biologics is a plus.
Familiarity with European, United States, and Japanese Pharmacopoeia.
Ability to apply quality requirements and follow approved procedures.
Proficiency in data systems for chromatography, such as Empower, and in spreadsheet and word‑processing tools.
Effective communication in French and English; organized, curious, eager to learn new techniques; thrives in a collaborative environment.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

SME (Subject Matter Expert) Energy Networks (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

Nous recherchons un·e SME (Subject Matter Expert) Energy Networks qui est analytique, orienté·e sécurité et collaboratif·ve pour rejoindre notre équipe basée sur notre campus à Braine-l’Alleud, Belgique.

À propos du rôle

Vous allez devenir l’expert·e technique et opérationnel·le garant·e de la performance, de la fiabilité, de la sécurité et de la conformité réglementaire des réseaux d’énergie (réseaux « bâtiments », « enterrés » et réseaux « enterrés tierces ») sur les trois sites belges d’UCB. Vous allez superviser la maintenance, soutenir les projets d’amélioration, assurer la continuité des énergies critiques et contribuer au respect strict des standards. Vous jouerez un rôle clé dans l’optimisation des infrastructures énergétiques et l’intégration de nouvelles technologies.

Avec qui vous allez collaborer

Vous allez travailler en étroite collaboration avec le Team Leader Energy Networks, les équipes techniques internes, les partenaires de maintenance, les services d’ingénierie, les sous-traitants et les organismes agréés. Votre quotidien reposera sur la coordination, la communication transparente et la collaboration pluridisciplinaire.

Ce que vous allez faire

· Vous allez coordonner la maintenance préventive, corrective et prédictive des réseaux d’énergie.

· Vous serez responsable de la planification des interventions majeures en garantissant sécurité et conformité.

· Vous allez gérer la documentation technique, les plans, schémas, rapports et dossiers as-built.

· Vous participerez aux projets de rénovation, extension et optimisation, du design jusqu’à la réception.

· Vous contribuerez à la gestion des risques, à la conformité réglementaire et à l’animation de la culture sécurité.

· Vous coordonnerez équipes internes, sous-traitants et fournisseurs pour assurer la continuité opérationnelle.

Intéressé·e ?

Pour ce rôle, nous recherchons les compétences et qualifications suivantes

· Bachelier en électromécanique (≥7 ans d’expérience) ou A2 (≥12 ans) sur sites industriels complexes.

· Maîtrise des réseaux électriques et bonne connaissance des réseaux gaz, eau, IT, égouts et géothermie.

· Expérience en maintenance, projets d’amélioration et coordination d’équipes internes et externes.

· Connaissance approfondie RGIE, GMP, HSE, ISO 14001/45001 et exigences réglementaires.

· Capacité à analyser les pannes, optimiser la performance énergétique et gérer les risques.

· Excellentes compétences en communication, leadership, gestion du changement et adaptation digitale.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Facilities Automation Engineer (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Facilities Automation Engineer who is proactive, solution-oriented, and digitally minded to join our Automation team, based at our UCB campus located in Braine-l’Alleud, Belgium.

Note that 3 roles are now open : 1 specialized in PCS7 (system engineer), 1 in Aveva SP (facilities engineer) and 1 for both (alarm engineer).

About the role

You are going to support, maintain, and evolve automated facilities systems across UCB’s Belgian sites. You will act as the technical expert and system owner for HVAC, fire detection, access control, and other facility-related automation systems. You will contribute to a digital-first, collaborative environment while ensuring reliability, compliance, and smooth handover to operations.

Who you will work with

You will collaborate with engineering, manufacturing, quality, IT, and external automation partners. You will work closely with multidisciplinary teams to align strategies, support daily operations, and ensure robust automation solutions across the site.

Major projects you could participate in

PCS7: We have 4 infrastructures in Belgium where PCS7 is used,in which there are numerous projects such as the implementation of new molecule production, new equipment, and production optimizations. We also have upgrade projects to keep installations up to date.
AVEVA SP: Projects to redefine all our infrastructures to integrate new buildings and installations: site utilities and new research facilities.

What you will do

· You will support and evolve facilities automation systems, ensuring reliability and compliance across Belgian sites.

· You will be responsible for developing and maintaining automation documentation, procedures, and software throughout asset lifecycle.

· You will manage collaboration with integrators and vendors during design, development, testing, and execution phases.

· You will participate in FAT, SAT, commissioning, validation, and 24/7 hybrid support with automation partners.

· You will lead alignment workshops and contribute to automation strategy, including HMI, reporting, and alarm philosophy.

· You will deliver training and ensure smooth handover to operations teams through a digital-first approach.

Evolution in the role

BelTech Automation was officially created in January 2025. It is a team under construction and expansion, with the ambition to align our support models for production and projects in Belgium.

This could lead to growth opportunities in technical, project, and management areas. The team currently consists of 15 internal members and more than 80 external collaborators.

Interested ?

For this role, we are looking for the following education, experience, and skills

· Master’s degree in automation with minimum 5 years of experience in the field.

· Strong competencies in AVEVA (mandatory), automation design, execution, commissioning, validation, and regulatory compliance. Knowledge of facilities and HVAC is seen as a nice to have.

· Ability to analyze complex technical issues and present clear, structured recommendations.

· Excellent communication, collaboration, leadership, and change-management skills in dynamic environments.

· Digital mindset with understanding of MES, monitoring platforms, data integrity, and cybersecurity fundamentals.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Facilities Automation Engineer (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

We are looking for a Facilities Automation Engineer who is proactive, solution-oriented, and digitally minded to join our Automation team, based at our UCB campus located in Braine-l’Alleud, Belgium.

About the role

Who you will work with

What you will do

· You will support and evolve facilities automation systems, ensuring reliability and compliance across Belgian sites.

· You will be responsible for developing and maintaining automation documentation, procedures, and software throughout asset lifecycle.

· You will manage collaboration with integrators and vendors during design, development, testing, and execution phases.

· You will participate in FAT, SAT, commissioning, validation, and 24/7 hybrid support with automation partners.

· You will lead alignment workshops and contribute to automation strategy, including HMI, reporting, and alarm philosophy.

· You will deliver training and ensure smooth handover to operations teams through a digital-first approach.

Interested ?

For this role, we are looking for the following education, experience, and skills

· Master’s degree in automation with minimum 5 years of experience in the field.

· Strong competencies in AVEVA (mandatory), automation design, execution, commissioning, validation, and regulatory compliance. Knowledge of facilities and HVAC is seen as a nice to have.

· Ability to analyze complex technical issues and present clear, structured recommendations.

· Excellent communication, collaboration, leadership, and change-management skills in dynamic environments.

· Digital mindset with understanding of MES, monitoring platforms, data integrity, and cybersecurity fundamentals.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Alarm Automation Engineer (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for an Alarm Automation Engineer who is proactive, collaborative, and digitally minded to join our Automation team, based at our UCB campus located in Braine-l’Alleud, Belgium.

Note that 3 roles are now open : 1 specialized in PCS7 (system engineer), 1 in Aveva SP (facilities engineer) and 1 for both (alarm engineer).

About the role

You will define, align, and standardize the alarm management strategy for the entire Braine site while acting as the technical expert and system owner for alarm-related automation systems. You will contribute to UCB’s digital-first culture by ensuring robust, compliant, and continuously improving automation systems.

Who you will work with

You will collaborate closely with engineering, manufacturing, quality, IT, and automation teams, as well as external partners and integrators. You will operate in a highly collaborative environment where cross-functional teamwork is key to delivering reliable, digital-ready manufacturing systems.

Major projects you could participate in

PCS7: We have 4 infrastructures in Belgium where PCS7 is used,in which there are numerous projects such as the implementation of new molecule production, new equipment, and production optimizations. We also have upgrade projects to keep installations up to date.
AVEVA SP: Projects to redefine all our infrastructures to integrate new buildings and installations: site utilities and new research facilities.

What you will do

· You will define and maintain site-wide alarm management strategy and documentation.

· You will be responsible for developing and improving automation procedures, software, and lifecycle documents.

· You will participate in multidisciplinary workshops aligning engineering, manufacturing, and quality stakeholders.

· You will manage the review and approval of integrator deliverables, anticipating risks and cost deviations.

· You will support FAT, SAT, commissioning, validation, and 24/7 hybrid support activities with integrators.

· You will organize and deliver training to operators and experts, ensuring smooth handover to operations.

Evolution in the role

BelTech Automation was officially created in January 2025. It is a team under construction and expansion, with the ambition to align our support models for production and projects in Belgium.

This could lead to growth opportunities in technical, project, and management areas. The team currently consists of 15 internal members and more than 80 external collaborators.

Interested? For this role, we are looking for the following education, experience, and skills

· Master’s degree in automation.

· Minimum 5 years of experience in process automation within a GMP environment (must have).

· Strong knowledge of PCS7 AND AVEVA (must have), cGMP, automation design, commissioning, validation, and alarm management principles.

· Proven ability to work in dynamic operational environments with excellent communication and facilitation skills.

· Strong digital mindset and familiarity with MES, monitoring platforms, data integrity, and cybersecurity.

· Fluency in French and English, with willingness to travel occasionally.

Be part for 24/7 guard support (level 2) in hybrid model with Automation Integrators and ready to travel a limited period of time.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Digital Technology QC and Process Development Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Digital Technology QC and Process Development Lead who is technically strong, collaborative, and passionate about driving digital transformation within laboratory environments to join our Quality Control (QC) and MSAT team at UCB, based in Braine-l’Alleud, Belgium.

About the Role

As the DT QC Lead, you will define and execute the digital technology roadmap for QC Laboratories and Process Development Laboratories. You will introduce innovative solutions that enhance efficiency, compliance, and scientific excellence—ensuring seamless delivery and resilience of critical digital systems. You will work closely with scientists, stakeholders, cross‑functional partners, and external vendors to elevate digital capabilities while maintaining strict GxP and cybersecurity compliance.

Who You’ll Work With

You will collaborate with QC and MSAT scientific users, Digital Technology (DT) partners, project managers, quality experts, and external technology vendors. You will also coordinate with cybersecurity teams, global DT functions, and internal business partners to ensure compliant, high‑performing digital operations across the lab ecosystem.

What You’ll Do

Develop and maintain a forward‑looking digital roadmap aligned with QC/MSAT business priorities and compliance needs.
Identify emerging technologies and propose innovative solutions that enhance laboratory efficiency and data integrity.
Lead implementation of digital platforms including LIMS, CDS, LES, data analytics tools, instrument connectivity, and workflow systems.
Manage cross‑functional project teams, resources, timelines, and vendor engagements to ensure end‑to‑end project success.
Ensure all digital initiatives adhere to GxP requirements, UCB standards, and cybersecurity expectations.
Serve as application owner for laboratory digital systems, ensuring reliable, compliant, high‑performing lifecycle management.
Coordinate incident management, system changes, release cycles, and continuous improvement activities across DT functions.
Oversee and optimize project and operational budgets while managing vendor quality and performance.
Act as the primary DT partner for QC and MSAT stakeholders, ensuring transparency, alignment, and strong value realization.

Interested? For this role we’re looking for:

Deep technical understanding of QC/MSAT lab systems (e.g., LIMS, chromatography, reporting tools, ERP QA modules).
Experience with data‑provisioning platforms and advanced analytical capabilities.
Strong background in solution design, implementation, and complex project management within lab environments.
Knowledge of GxP‑compliant operations, ideally within the pharmaceutical industry.
Ability to translate complex technical concepts into clear, impactful communication.
Ability to collaborate effectively in global, cross‑functional teams; fluent English required.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

External Analytical Operations Support Specialist (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for an External Analytical Operations Support Specialist Specialist who is proactive, adaptable, and committed to excellence to join our Analytical Lifecycle Expertise & Integration team, based at our UCB campus in Braine‑l’Alleud, Belgium.

About the role

You will provide operational and analytical support to Contract Manufacturing Organizations (CMOs) across the lifecycle of UCB products. You will partner closely with internal teams and external vendors to ensure compliance, efficiency, and quality in analytical processes.

Who you will work with

You will collaborate with UCB Analytical Program teams, External Manufacturing, Quality Control, and Quality Assurance, as well as CMO partners worldwide. Together, you will ensure analytical excellence and inspection readiness.

What you will do

Provide expert advice and operational support for global analytical methods lifecycle
Review analytical aspects in deviations and change controls at CMOs
Support investigations for OOS/OOT/OOE and complex analytical issues
Coordinate cross‑laboratory studies and validation campaigns
Ensure compliance with GMP requirements and inspection readiness
Manage analytical documentation access for CMOs
Review annual stability protocols and tables/reports, results evaluation, trending reports, and documentation in EDMS system
Act as an informal leader by driving alignment across stakeholders, fostering collaborative problem‑solving, and proactively steering activities that support analytical lifecycle strategy
Influence without authority by guiding CMO partners and internal teams toward best practices, consistent quality standards, and timely execution

Interested? For this role, we are looking for the following education, experience, and skills

Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or related field
Strong knowledge of analytical techniques (HPLC, GC, ELISA, Bioassay, etc.)
Solid understanding of GMP, regulatory requirements, and Data Integrity principles
Excellent problem‑solving and troubleshooting skills
Ability to work independently and influence internal and external stakeholders
Strong communication skills in English
Able to effectively influence internal and external stakeholders, driving consensus and ensuring adoption of standardized and harmonized ways of working — while formal people management is not required, a leadership mindset is highly valued

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head of Supply Chain Data & Insight (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Head of Supply Chain Data & Insight who is strategic, forward‑thinking, and inclusive to join our Global Supply Chain Excellence team, based at our UCB campus located in Braine-l'Alleud, Belgium

About the role:

In this senior global role, you will shape and execute the enterprise‑wide Data, Analytics, Artificial Intelligence and Insight strategy for Supply Chain. You will build a modern, AI‑driven ecosystem that drives decision‑making, strengthens operational excellence, and unlocks business value across Patient Supply and Global Supply Chain. You will lead teams, elevate data governance, and ensure the availability of high‑quality, compliant, and trusted data to power a next‑generation supply chain.

Who you will work with:

You will collaborate closely with leaders across Global Supply Chain, Digital Technology, Quality, Finance, Procurement, Manufacturing, and other key business partners. You will act as the senior representative for Supply Chain on enterprise‑wide data and AI initiatives, influencing strategy and steering cross‑functional transformation. Your work will empower teams and help accelerate a culture of insight‑driven, AI‑enabled performance.

What you will do :

You will shape and drive the global Data, Analytics & AI strategy and multiyear roadmap for Supply Chain.
You will be responsible for governing AI, scaling predictive and prescriptive solutions, and embedding industry best practices.
You will manage data integrity, data quality, KPI frameworks, governance processes, and a single source of truth for Supply Chain.
You will oversee master data management, commercial labelling data operations, reporting services, and analytics delivery.
You will lead cross‑functional collaboration to ensure data and AI solutions create measurable value across the end‑to‑end Supply Chain.
You will develop talent, build capabilities, and foster an insight‑driven, AI‑enabled culture of continuous improvement.

Interested? For this role, we are looking for the following education, experience, and skills:

Bachelor’s or Master’s degree; APICS, CAP, or CDMP certification is considered a strong asset.
Minimum 10 years of experience in supply chain data and analytics, with deep understanding of end‑to‑end supply chain.
Expertise in data governance, data quality, data modelling, KPI frameworks, and analytics or AI/ML implementation.
Experience working with enterprise ERP systems and managing master data, labelling data, and reporting operations.
Strong leadership, influencing, and storytelling skills, with ability to translate complex topics for diverse audiences.
Growth‑minded, curious, collaborative, and comfortable leading transformation in data‑ and AI‑driven environments.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technicien(ne) Downstream (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Technicien·ne Downstream qui est rigoureux·se, proactif·ve et orienté·e solution pour rejoindre notre équipe Bio & GT Clinical Manufacturing Sciences (BGCMS), basée sur notre campus UCB à Braine-L’Alleud, Belgique.

À propos de votre rôle :

En tant que Technicien·ne Downstream, vous jouerez un rôle clé dans la production de protéines en phase de développement au sein du Bio Pilot Plant de Braine-L’Alleud. Vous travaillerez dans un environnement innovant, en utilisant des équipements de purification / buffers, tout en respectant les normes GMP (Good Manufacturing Practice) et HSE (Health, Safety, Environment) en vigueur.

Vous collaborerez avec :

Vous intégrerez une équipe dynamique et engagée, en lien étroit avec le responsable d’activité, les collègues de production, les équipes qualité et les parties prenantes internes et externes.

Vos activités :

Participer à la production de protéines à partir de cultures cellulaires, en appliquant les normes GMP, HSE et les procédures internes (chromatographie, ultrafiltration, filtration, inactivation virale, etc.)
Utiliser les équipements et logiciels de production pour réaliser les différentes étapes du process (Unicorn, PCS7, LIMS, XFP) et effectuer les analyses en cours de production (pH, conductivité, UV, tests de filtre)
Identifier et mettre en œuvre des améliorations techniques pour optimiser la production et la qualité
Contribuer à la documentation, à la création et à la revue des procédures, ainsi qu’à la complétude des dossiers de production
Collaborer avec l’équipe, répondre aux questions techniques, accompagner les collègues et participer à leur formation
Assurer le respect des bonnes pratiques de sécurité, ainsi que la vérification quotidienne des paramètres environnementaux

Intéressé·e ? Pour ce poste, nous recherchons la formation, l’expérience et les compétences suivantes :

Diplôme scientifique (biotechnologie, biochimie, etc.) et/ou certification équivalente
Expérience dans la purification de protéines (chromatographie, filtration frontale et tangentielle, etc.)
Maitrise du français (oral et écrit) et niveau intermédiaire en anglais (écrit)
Capacité à travailler de façon autonome, à adapter ses priorités et horaires selon les besoins
Aisance à évoluer dans un environnement dynamique et non routinier
Excellent esprit d’équipe
Sens de l’organisation, rigueur et respect des procédures qualité et sécurité

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Technicien(ne) Downstream (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

À propos de votre rôle :

Vous collaborerez avec :

Vos activités :

Participer à la production de protéines à partir de cultures cellulaires, en appliquant les normes GMP, HSE et les procédures internes (chromatographie, ultrafiltration, filtration, inactivation virale, etc.)
Utiliser les équipements et logiciels de production pour réaliser les différentes étapes du process (Unicorn, PCS7, LIMS, XFP) et effectuer les analyses en cours de production (pH, conductivité, UV, tests de filtre)
Identifier et mettre en œuvre des améliorations techniques pour optimiser la production et la qualité
Contribuer à la documentation, à la création et à la revue des procédures, ainsi qu’à la complétude des dossiers de production
Collaborer avec l’équipe, répondre aux questions techniques, accompagner les collègues et participer à leur formation
Assurer le respect des bonnes pratiques de sécurité, ainsi que la vérification quotidienne des paramètres environnementaux

Intéressé·e ? Pour ce poste, nous recherchons la formation, l’expérience et les compétences suivantes :

Diplôme scientifique (biotechnologie, biochimie, etc.) et/ou certification équivalente
Expérience dans la purification de protéines (chromatographie, filtration frontale et tangentielle, etc.)
Maitrise du français (oral et écrit) et niveau intermédiaire en anglais (écrit)
Capacité à travailler de façon autonome, à adapter ses priorités et horaires selon les besoins
Aisance à évoluer dans un environnement dynamique et non routinier
Excellent esprit d’équipe
Sens de l’organisation, rigueur et respect des procédures qualité et sécurité

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Technicien.ne de maintenance Utilities (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

Nous recherchons un/e Technicien/e de maintenance Utilities qui est minutieux/se, proactif/ve et collaboratif/ve pour nous rejoindre sur notre campus de Braine-l'Alleud, Belgique.

À propos du rôle

Avec qui vous allez travailler

Ce que vous allez faire

Vous participez aux améliorations et développements des installations Utilities.
Vous effectuez la maintenance préventive et curative des équipements.
Vous signalez toute anomalie, erreur ou incident à la hiérarchie.
Vous préparez et rédigez des instructions de maintenance et des dossiers techniques.
Vous assurez la documentation pré et post opérations de maintenance.
Vous suivez les règles GMP et GLP et maintenez les normes de sécurité et environnementales.

Intéressé/e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes

Minimum un A2 dans le domaine technique avec minimum 3 à 5 ans d’expérience dans la maintenance d’équipements ou un bachelier en électromécanique.
Expérience antérieure dans une société pharmaceutique ou agro-alimentaire souhaitée.
Connaissance approfondies des utilities (vapeur, eau, chauffage, ventilation) et techniques du froid, HVAC.
Capacité à lire et interpréter des dessins électriques, mécaniques, pneumatiques et hydrauliques.
Très bonne connaissance du français ; connaissance pratique de l'anglais technique est un plus.
Pragmatique, rigoureux et capable de travailler en autonomie.
Bon esprit d'équipe et compétences communicationnelles.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Technicien.ne de maintenance Utilities (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un/e Technicien/e de maintenance Utilities qui est minutieux/se, proactif/ve et collaboratif/ve pour nous rejoindre sur notre campus de Braine-l'Alleud, Belgique.

À propos du rôle

Avec qui vous allez travailler

Ce que vous allez faire

Vous participez aux améliorations et développements des installations Utilities.
Vous effectuez la maintenance préventive et curative des équipements.
Vous signalez toute anomalie, erreur ou incident à la hiérarchie.
Vous préparez et rédigez des instructions de maintenance et des dossiers techniques.
Vous assurez la documentation pré et post opérations de maintenance.
Vous suivez les règles GMP et GLP et maintenez les normes de sécurité et environnementales.

Intéressé/e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes

Minimum un A2 dans le domaine technique avec minimum 3 à 5 ans d’expérience dans la maintenance d’équipements ou un bachelier en électromécanique.
Expérience antérieure dans une société pharmaceutique ou agro-alimentaire souhaitée.
Connaissance approfondies des utilities (vapeur, eau, chauffage, ventilation) et techniques du froid, HVAC.
Capacité à lire et interpréter des dessins électriques, mécaniques, pneumatiques et hydrauliques.
Très bonne connaissance du français ; connaissance pratique de l'anglais technique est un plus.
Pragmatique, rigoureux et capable de travailler en autonomie.
Bon esprit d'équipe et compétences communicationnelles.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Stability Operations Partner (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Stability Operations Partner organisé·e, proactif·ve et orienté·e qualité, pour rejoindre notre équipe Stability Operations, basée sur notre campus UCB situé à Braine‑l’Alleud, Belgique.

À propos du rôle

Vous allez jouer un rôle clé dans la coordination et l’exécution des activités de stabilité et de gestion des échantillons pour les Drug Substances biologiques. Vous assurerez la prise en charge complète des échantillons, dès leur réception jusqu’à la fin de leur cycle de vie, dans le respect strict des exigences GMP. Vous contribuerez directement à la qualité des produits, à la conformité réglementaire et aux initiatives d’amélioration continue.

Avec qui vous travaillerez

Vous travaillerez en étroite collaboration avec les laboratoires QC, les équipes de fabrication, les services analytiques, la supply chain et la Quality Assurance. Vous interagirez quotidiennement avec des équipes internes à l’échelle internationale ainsi qu’avec des partenaires externes tels que les laboratoires sous contrat (CLO), fournisseurs et prestataires. Vous participerez également à des projets d’amélioration des processus et des systèmes.

Ce que vous ferez

Vous allez coordonner les activités de stabilité des lots biologiques, de la réception jusqu’à la fin du cycle de vie des produits.
Vous serez responsable de la réception, de l’aliquotage, de la gestion des stocks, du pulling et de la distribution des échantillons.
Vous allez créer et gérer les études et protocoles de stabilité dans le LIMS et lancer les stabilités.
Vous allez gérer la distribution interne, les expéditions externes, le suivi des COA et la résolution des incidents.
Vous allez assurer le suivi de la maintenance des enceintes climatiques.
Vous allez contribuer aux déviations, investigations, audits et projets d’amélioration continue.

Intéressé·e ? Pour ce rôle, nous recherchons l’éducation, l’expérience et les compétences suivantes :

Baccalauréat dans un domaine scientifique ou de laboratoire.
Expérience dans un environnement réglementé GMP ou pharmaceutique.
Connaissances analytiques des produits NCE et NBE.
Expérience en stabilité ou en gestion d’échantillons est un atout important.
Capacité à travailler de manière autonome tout en collaborant transversalement.
Anglais écrit et lu requis ; la maîtrise est un avantage.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Stability Operations Partner (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

À propos du rôle

Avec qui vous travaillerez

Ce que vous ferez

Vous allez coordonner les activités de stabilité des lots biologiques, de la réception jusqu’à la fin du cycle de vie des produits.
Vous serez responsable de la réception, de l’aliquotage, de la gestion des stocks, du pulling et de la distribution des échantillons.
Vous allez créer et gérer les études et protocoles de stabilité dans le LIMS et lancer les stabilités.
Vous allez gérer la distribution interne, les expéditions externes, le suivi des COA et la résolution des incidents.
Vous allez assurer le suivi de la maintenance des enceintes climatiques.
Vous allez contribuer aux déviations, investigations, audits et projets d’amélioration continue.

Intéressé·e ? Pour ce rôle, nous recherchons l’éducation, l’expérience et les compétences suivantes :

Baccalauréat dans un domaine scientifique ou de laboratoire.
Expérience dans un environnement réglementé GMP ou pharmaceutique.
Connaissances analytiques des produits NCE et NBE.
Expérience en stabilité ou en gestion d’échantillons est un atout important.
Capacité à travailler de manière autonome tout en collaborant transversalement.
Anglais écrit et lu requis ; la maîtrise est un avantage.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

BIO DS Quality Operation Superviseur Week-End (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Pour renforcer notre Quality Bio DS, nous recherchons un profil talentueux pour occuper le poste de : Superviseur Qualité des Opérations Bio DS Week-End – Braine-l'Alleud, Belgique.

À propos du poste

Le/La Superviseur(e) Qualité Bio DS est responsable des activités d’assurance qualité liées aux opérations de fabrication USP dans la nouvelle usine de production de substances biologiques commerciales d'UCB à Braine. Ce rôle crucial garantit la conformité aux normes internes, promeut l'amélioration continue des processus de qualité et dirige une équipe de GMP Facilitateurs pour maintenir les normes les plus élevées de qualité et de sécurité des produits.

En phase de lancement de la nouvelle usine, le/la superviseur(e) doit diriger activement l'équipe, s'adapter aux défis initiaux et collaborer avec les départements appropriés pour assurer l'alignement avec la production.

Vous travaillerez avec

Le/La superviseur(e) travaillera étroitement avec les équipes de production ,maintenance, logistique, ainsi que les responsables de la conformité réglementaire et les auditeurs pour garantir le respect des normes de qualité et de sécurité.

Ce que vous ferez

Leadership et Management

Diriger et gérer l'équipe d’USP GMP Facilitators, y compris le planning, le recrutement, la formation et la gestion des performances.
Assurer que les batch records, les audit internes et la préparation des documents nécessaires au release des lots sont suivis de façon précise et dans les temps. Cela en mettant en place et en appliquant des outils de planification permettant le suivi de l’équipe.
Définir les points de développement et de connaissances de l’équipe.
Gérer les horaires de l’équipe qui travaille pause de journée (6h-14h et 14h-22h) en semaine et en week-end.
Gérer la communication avec l’équipe et maintenir sa motivation.
Former et coacher l’ensemble de l’équipe afin d’atteindre un niveau d’expérience process et qualité élevé.
Participer aux réunions mis en place par le département qualité.

Quality Assurance

Assurer que les équipes de production USP soit imprégner de la culture qualité et de l’amélioration continue.
Réaliser le release des lots de production d’intermédiaires.
Assurer un oversight qualité adéquat sur les documents et activités GMP grâce à la présence QA sur le terrain.
Revoir et donner un input terrain afin d’améliorer les SOP et les Master Batch records.
Revoir et approuver les déviations mineures, les changes control et les actions correctives et préventives.
Participer activement au gouvernance production et de l’organisation QA et cascader toutes les informations nécessaires aux GMP Facilitators.
Assurer que les problèmes rencontrés sur le terrain sont traités ou escalader au bon niveau de management.

Intéressé(e) ?

Diplômé(e) de l’enseignement supérieur de type Bachelier/Master (biotechnologie, chimie, etc.)

Vous devez avoir déjà travaillé dans un environnement conforme aux Bonnes Pratiques de Fabrication (GMP).
Vous devez posséder au moins 5 ans d'expérience dans les procédés de production biotechnologiques, que ce soit Upstream ou Downstream.
Vous devez avoir de solides connaissances des systèmes qualité, notamment en ce qui concerne les déviations, les CAPA (Corrective and Preventive Actions) et le Change Control.
Vous devez démontrer une expérience significative en gestion d'équipe.
Vous devez avoir d'excellentes compétences en communication orale et écrite.
Vous devez avoir une aptitude marquée pour la collaboration et un bon esprit d'équipe.
Vous devriez assurer votre présence lors des jours fériés
Vous travaillerez le week-end, en horaire de jour, du samedi au lundi

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Early Assets Supply Lead (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for an Early Asset Supply Lead who is strategic, collaborative, and solution-oriented to join our Global Supply Chain team, based at our UCB campus located in Braine-l’Alleud, Belgium.

About the role:

You will drive the transition of early‑stage assets from development to commercial launch while shaping supply, inventory, and capacity strategies for future product readiness. You will ensure supply resilience, support lifecycle management, and orchestrate long‑range planning activities that help us meet patient and business objectives.

Who you will work with

You will collaborate with Patient Supply teams, technical teams, manufacturing partners, and cross‑functional stakeholders involved in launch excellence, compliance, asset strategy, and long‑range planning. You will work across functional boundaries to align on assumptions, manage risks, strengthen supply resilience, and prepare assets for their full lifecycle.

What you will do:

You will ensure the smooth transition of assets supply management from development to commercial environments.
Progressively integrate early assets into established supply chain and asset governance processes, adapting them to early-stage realities.
You will be responsible for integrating demand, supply, and inventory decisions to build a robust supply network strategy.
You will translate long‑range demand plans into long‑range supply requirements to support network definition.
You will manage strategic supply, inventory, and capacity scenarios while identifying risks and mitigation actions.
You will develop and execute asset supply and launch strategies in close partnership with internal stakeholders.
You will represent Supply Chain in key compliance and change control forums, ensuring alignment and risk escalation
Operate with autonomy, proactively engaging stakeholders and demonstrating value through influence rather than formal authority.

Interested? For this role, we are looking for the following education, experience, and skills:

Bachelor’s or Master’s degree in a relevant field; advanced degree beneficial.
Strong understanding of end‑to‑end supply chain processes, supply chain planning, and strategic business requirements.
Ability to link commercial expectations to supply, capacity, and inventory implications early in the asset lifecycle.
Experience in process definition, change management, and compliance frameworks (GMP, GDP, trade regulations).
Ability to work cross‑functionally and deliver innovative, value‑driving solutions.
Excellent written and verbal communication skills with diverse technical and non‑technical audiences.
Prior exposure to biologics, CMC, or clinical supply environments is considered a plus.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Pharmacometrics Team Lead (Belgium) (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

About the role

Who you’ll work with

Working closely with the QCP Leads assigned to the various projects, to ensure clear integration of the pharmacometrics aspects into the programs.

What you’ll do

Coaching and mentoring junior staff on how to navigate within a project and matrix organization.
Leading and delivering the Pharmacometrics strategy to support development of our assets. extrapolation (where appropriate), dose selection, trial design, PIP development and ongoing evaluation of data as generated.
Performing hands-on population PK/PD, exposure-response modeling and clinical trial simulations on an assigned project.
Developing submission ready fit for purpose Pharmacometrics analysis plans and reports.
Initiating and overseeing outsourced pharmacometrics activities and further internalizing the work as needed.
Having a working knowledge about the regulatory pathways on a global basis and opportunities for collaboration with health authorities (either through working parties, advice meetings, and other initiatives) in pediatrics, Neurology and Immunology.
Promoting MID3 internally and externally.

Interested? For this role you’ll need the following education, experience and skills

Doctorate (PhD or MD) in the related disciplines of Pharmaceutical Sciences, Statistics or Engineering.
8+ years (Bio)pharmaceutical industry experience in Pharmacometrics with minimum of 2 years line management responsibilities.
Hands-on experience in population PK/PD, disease progression modeling, and clinical trial simulations.
Strong understanding and knowledge of Bayesian methodologies, model-based meta-analyses, PBPK, QSP, and AI/ML in Pharmacometrics.
Expertise in R, NONMEM or related pharmacometrics software.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Employé technique en production chimique (CDI lié à la durée du projet, confirmé jusqu'en 2029) (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un Employé Technique en Production Chimique qui est formé sur le secteur de production pharmaceutique, a un bon esprit d’équipe et respecte les procédures pour rejoindre notre équipe de production Chimique, basée dans notre campus de Braine-l’Alleud, Brabant Wallon, Belgique.

Le poste est pour un contrat CDI dont la pérennité est directement liée à la durée du projet, actuellement confirmé jusqu’en 2029.qui suit un horaire de feu continu sur 3 shifts : 6heure-14heure, 14heures-22heures, 22heures- 6heures.

Raison d’Être de la Fonction :

Le titulaire du poste a pour mission d'exécuter les opérations nécessaires pour atteindre les objectifs de production tout en assurant le bon déroulement technique et documentaire de la fabrication de nos produits, dans le respect des normes de sécurité et des bonnes pratiques GMP et HSE. En l'absence du chef d'équipe, il prend également en charge certaines responsabilités de supervision.

Tâches Principales :

En tant qu'Employé Technique en Production Chimique, vos responsabilités incluent :

Réaliser de manière autonome les opérations liées à plusieurs synthèses, notamment les chargements, réactions, extractions, purifications, cristallisations, précipitations, filtrations, essorages, séchages, et conditionnements.
Maîtriser l'intégralité du processus de l'une ou plusieurs synthèses.
Mettre en place les équipements en mode sécurité de manière autonome.
Compléter les fiches de fabrication, enregistrer les paramètres et tenir les journaux de bord, en collectant les données pertinentes telles que les graphiques, etc.
Assurer la propreté des installations en effectuant les nettoyages nécessaires.
Effectuer une double vérification des phases critiques.
Selon la charge de travail et l'organisation, réaliser d'autres tâches sous la supervision éventuelle d'un autre chef d'équipe, telles que l'entretien des installations, etc.
Contrôler les documents d'enregistrement des données brutes, tels que les journaux de bord et les fiches de fabrication.
Participer aux validations, qualifications, et industrialisations de nouvelles opérations ou processus.
Ajuster les paramètres dans le système de supervision selon les normes existantes en cas de besoin.
Effectuer des interventions de maintenance de premier niveau de manière autonome.
Respecter et faire respecter les normes de sécurité et les bonnes pratiques de fabrication (GMP).
Identifier et signaler les problèmes techniques, de processus ou liés à la sécurité, en proposant des solutions appropriées et en participant à leur résolution.
Être capable de gérer un procédé en cas de perturbation non récurrente en toute sécurité.
Participer au suivi terrain de travaux importants sans avoir la responsabilité des ouvertures/fermetures.
Pouvoir travailler en autonomie sur la synthèse dont il s'occupe en cas d’absence de courte durée du chef d’équipe.
Proposer des améliorations continues sur l'ensemble des tâches/activités de l'équipe et en assurer le suivi tout en accomplissant les tâches quotidiennes.
Consulter la documentation technique si nécessaire et codifier des équipements.
Être responsable de sa zone de travail selon les normes "5S" et veiller à son respect du processus.

Exigences du Poste :

Expérience préalable en production chimique ou formation de terrain telle que la formation Aptaskil est un atout
Maîtrise des bonnes pratiques GMP et des normes de sécurité HSE.
Capacité à travailler de manière autonome
Bon esprit d’équipe
Respect des procédures

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Aseptic & Bio-Process Validation Manager (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Aseptic&Bio-Process Validation Manager orienté·e qualité, centré·e sur les personnes et proactif·ve pour rejoindre notre équipe basée sur notre campus UCB de Braine‑l’Alleud, Belgique.

À propos du rôle

En tant que Aseptic&Bio-Process Validation Manager, vous gérerez et encadrerez l'unité « Aseptic et Gene Therapies » du service Qualification & Validation de notre entité Belge. Vous garantirez l'état qualifié et validé des équipements, systèmes et procédés utilisés dans les activités commerciales et de développement de votre pôle d’activité.

Vous apporterez également votre expertise en qualification/validation et gérerez les ressources pour soutenir les activités de routine et les projets en conformité avec le plan directeur de Validation du Site.

Avec qui vous travaillerez

Vous collaborerez étroitement avec QA, IT, Métrologie, Ingénierie, propriétaires de systèmes, producteur, automation, ainsi qu’avec des fournisseurs externes. Vous représenterez votre BU en audits/inspections (FDA, AFMPS/EMEA) et soutiendrez la culture Patient et EHS sur l’ensemble du campus.

Ce que vous ferez

Vous allez définir et déployer la stratégie de qualification/validation pour équipements, systèmes, utilités et procédés aseptiques & bio‑process, en ligne avec les benchmarks de l’industrie.
Vous allez Diriger la BU (~10 FTE) : organisation, priorités, ressources (internes/externes), développement des compétences, onboarding, coaching.
Vous allez assurer la validation des procédés (culture, purification, préparation milieux), CSV, nettoyage/stérilisation, et la qualification des utilités/HVAC.
Vous allez maintenir l’“auditabilité” documentaire et les systèmes qualité (déviations, CAPA, change control), en garantissant la conformité cGMP/HSE.
Vous allez soutenir et mettre à jour le SVMP, définir des KPI pertinents, et piloter l’exécution (routine & projets) dans les délais et budgets.
Vous allez animer la relation avec les parties prenantes (internes/externes) et représenter la BU en comités, audits et inspections.

Intéressé·e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes :

Master (ou équivalent) en domaine pertinent ; 10+ ans en qualification/validation pharmaceutique (aseptique, bio‑process, CSV, utilités/HVAC).
Maîtrise des approches Verification/ASTM E2500, de l’analyse de risques et de la documentation cycle V.
Solide pratique des systèmes qualité et des audits/inspections (préparation, réponses, suivi).
Gestion de portefeuilles validation routine + projets (planification, priorisation, budget), alignée sur SVMP.
Français et anglais courants (écrit/oral).

Orientation qualité/patient et compliance by design ; culture EHS ancrée.

Leadership inclusif, coaching, développement des talents, capacité à décider et prioriser sous contrainte, expérience démontrée en management d’équipe (~10 personnes), communication et influence multi‑parties prenantes.

Interaction fournisseurs et négociation efficaces ; sens du service et de la collaboration.
Esprit d’innovation et d’amélioration continue ; structuration de process et inspection readiness permanente.

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Team Leader Biomanufacturing - Media & Buffer (week-end / jour) (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un.e Team Leader Biomanufacturing – Media Buffer (week-end shift de jour) talentueux.se et motivé.e pour rejoindre notre Belgium Biomanufacturing Operations Center à Braine-L’Alleud, Belgique.

Le rôle s’effectue à 100% sur site et comprend des horaires en shift, du vendredi au dimanche ou du samedi au lundi (6h-14h et 14h-22h).

Concernant le rôle :

En tant que Team Leader Media Buffer, vous jouerez un rôle clé dans la supervision et l’optimisation des activités de production Buffer & Media. Vous serez responsable de la coordination des opérations, du respect des normes de sécurité et de qualité, et de l’amélioration continue des processus. Ce poste s’inscrit dans un environnement dynamique et collaboratif, où l’accompagnement des équipes et la communication sont essentiels.

Vous travaillerez avec :

Vous travaillerez au quotidien avec une équipe de technicien.ne.s que vous accompagnerez, en collaboration étroite avec les fonctions supports telles que l’assurance qualité, le contrôle qualité, la maintenance et la validation, ainsi qu’avec les nouveaux.elles arrivant.e.s que vous intégrerez et formerez, afin de garantir la continuité, la performance et l’amélioration continue des activités de production.

Vos activités :

Organiser et gérer le planning de production, les horaires et la gestion des installations
Apporter un soutien à l’équipe pour la réalisation des activités de production
Appliquer et faire respecter les règles de sécurité, d’hygiène et de qualité
S’assurer que le personnel est formé et que les équipements sont qualifiés, calibrés et maintenus
Communiquer clairement les informations importantes et signaler les problèmes critiques
Collaborer avec les fonctions supports pour garantir la continuité des opérations
Prendre en charge les actions immédiates en cas de dysfonctionnement ou d’anomalie
Initier et documenter les incidents qualité et EHS (Environment, Health, Safety), et participer aux investigations
Identifier et soutenir des actions d’amélioration continue pour optimiser la production
Participer à l’intégration et à l’accompagnement des nouveaux.elles membres de l’équipe

Intéressé.e ? Pour ce poste, nous recherchons la formation, l’expérience et les compétences suivantes :

Expérience en biotechnologie ou industrie pharmaceutique
Expérience confirmée en management d’équipe
Bonne connaissance des GMP (Good Manufacturing Practice) et des standards qualité
Capacité à faire face à des situations urgentes et prendre des décisions à son niveau
Capacité à travailler dans un environnement dynamique
Excellent esprit d’équipe
Excellentes compétences en Français, niveau intermédiaire en Anglais

#Biomanufacturing

Êtes-vous prêt à « aller au-delà » pour créer de la valeur et faire la différence pour les patients ? Si cela vous parle, alors nous aimerions vous connaitre !  

À propos de nous  

Pourquoi travailler pour nous ?

Team Leader Biomanufacturing - Media & Buffer (week-end / jour) (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

Nous recherchons un.e Team Leader Biomanufacturing – Media Buffer (week-end shift de jour) talentueux.se et motivé.e pour rejoindre notre Belgium Biomanufacturing Operations Center à Braine-L’Alleud, Belgique.

Le rôle s’effectue à 100% sur site et comprend des horaires en shift, du vendredi au dimanche ou du samedi au lundi (6h-14h et 14h-22h).

Concernant le rôle :

Vous travaillerez avec :

Vos activités :

Organiser et gérer le planning de production, les horaires et la gestion des installations
Apporter un soutien à l’équipe pour la réalisation des activités de production
Appliquer et faire respecter les règles de sécurité, d’hygiène et de qualité
S’assurer que le personnel est formé et que les équipements sont qualifiés, calibrés et maintenus
Communiquer clairement les informations importantes et signaler les problèmes critiques
Collaborer avec les fonctions supports pour garantir la continuité des opérations
Prendre en charge les actions immédiates en cas de dysfonctionnement ou d’anomalie
Initier et documenter les incidents qualité et EHS (Environment, Health, Safety), et participer aux investigations
Identifier et soutenir des actions d’amélioration continue pour optimiser la production
Participer à l’intégration et à l’accompagnement des nouveaux.elles membres de l’équipe

Intéressé.e ? Pour ce poste, nous recherchons la formation, l’expérience et les compétences suivantes :

Expérience en biotechnologie ou industrie pharmaceutique
Expérience confirmée en management d’équipe
Bonne connaissance des GMP (Good Manufacturing Practice) et des standards qualité
Capacité à faire face à des situations urgentes et prendre des décisions à son niveau
Capacité à travailler dans un environnement dynamique
Excellent esprit d’équipe
Excellentes compétences en Français, niveau intermédiaire en Anglais

#Biomanufacturing

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Risk & Compliance Manager (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Risk & Compliance Manager who is strategic, influential, and analytically strong to join our Global Supply Chain Excellence team, based at our UCB campus located in Braine-l’Alleud, Wallonia, Belgium.

About the role:

In this role, you will shape and lead risk and compliance governance across UCB’s Global Supply Chain. You are going to drive how risks are identified, assessed, and mitigated while strengthening audit readiness and regulatory compliance. You will act as a trusted partner across functions, enabling informed decision-making, simplifying processes, and embedding a strong risk and compliance culture throughout the organization. .

Who you will work with:

You will work closely with the Global Supply Chain risk community, Quality, Regulatory, Excellence, and Patient Supply teams. You are going to collaborate with senior stakeholders, process owners, and cross‑functional partners worldwide. Together, you will strengthen governance frameworks, share regulatory intelligence, and ensure supply chain ownership in enterprise-wide initiatives.

What you will do:

You will own and govern the Global Supply Chain risk portfolio end to end, ensuring alignment with Patient Supply risk management frameworks.
You will lead the Global Supply Chain risk community, onboarding, coaching, and strengthening risk management capabilities across stakeholders.
You will coordinate and facilitate the full risk management cycle, including risk identification, assessment, mitigation, and escalation.
You will consolidate key risks and ensure effective response strategies and mitigation plans are implemented and tracked.
You will monitor compliance KPIs (deviations, CAPAs, training, documentation) and drive continuous improvement to ensure audit readiness.
You will coordinate audits and inspections, and support the preparation, execution, and follow-up of audit outcomes.
You will lead or contribute to Quality Management Reviews, consolidating observations and ensuring effective CAPA management.
You will oversee Supply Chain documentation practices, including SOPs and Quality Management Systems, ensuring compliance with GMP/GDP standards.
You will act as liaison for Regulatory Intelligence activities, ensuring insights are assessed, translated into actions, and embedded into Supply Chain processes.
You will represent Global Supply Chain in governance forums, regulatory networks, and cross-functional compliance initiatives.
You will support process owners in strengthening documentation, training, and compliance practices across the organization.
You will drive continuous improvement initiatives to simplify processes, strengthen governance, and enhance compliance awareness across Global Supply Chain.

Interested? For this role, we are looking for the following education, experience, and skills:

Bachelor’s or Master’s degree in a relevant discipline.
Around 10 years of experience in the pharmaceutical industry with strong GMP/GDP exposure.
Proven experience in Quality, Regulatory, Compliance, Governance, or Risk Management environments.
Strong understanding of GxP processes including deviations, CAPA, change control, and audit management.
Demonstrated ability to lead cross-functional initiatives and influence stakeholders without authority.
Experience driving change, governance frameworks, and continuous improvement in complex environments.
Strong analytical and problem-solving skills with the ability to translate complexity into actionable insights.
Excellent communication and facilitation skills, with experience engaging senior stakeholders.
Strong planning and prioritization capabilities with a balance of strategic thinking and operational execution.
Fluency in English and French, with confidence in multicultural environments.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head of QA Analytical Services (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Head of QA Analytical Services who is strategic, collaborative, and quality-driven to join our QA Analytical Services team within Pharma & Injectable Quality, based at our UCB campus in Braine-l’Alleud, Wallonia, Belgium.

This is a site-based leadership role focused on the Braine operations.

About the role

In this role, you will lead the QA Analytical Services team and ensure that Quality Control (QC) systems, processes, and operations at the Braine site meet applicable global regulatory standards. You will drive compliance, data integrity, continuous improvement, and quality leadership across QC activities. You will play a key role in developing robust systems, supporting inspections, and enabling high-performance analytical services within a complex, regulated environment.

Who you will work with

You will work closely with QC Management, Analytical Science, QA partners, and cross-functional teams within the Braine site, while aligning with global standards and corporate functions when required. You will collaborate with system owners, project teams, internal customers, and regulatory inspection stakeholders to maintain a strong state of compliance and control. You will also coach, mentor, and develop a diverse team of QA professionals.

What you will do :

You will lead the QA Analytical Services team, ensuring strong performance, development, coaching, and alignment with business priorities.
You will ensure that QC systems, operations, and processes comply with global regulations (EMEA, FDA, PIC/S, ICH) and UCB standards.
You will manage QC quality systems activities, including deviations, investigations, change control, validation, audits, and documentation.
You will drive continuous improvement, identifying and implementing opportunities to enhance compliance, quality KPIs, and operational excellence.
You will prepare QC teams for inspections and act as a key contributor during audits and regulatory interactions.
You will oversee data integrity, analytical system compliance, and risk‑based quality decision‑making across QC activities.

Interested? For this role, we are looking for the following education, experience, and skills

Minimum 10 years in a regulated pharmaceutical, life‑science, or health‑related environment, including 5 years in QA and 5 in QC.
Strong expertise in QC laboratory operations, analytical techniques, and relevant international regulations.
Proven leadership experience managing a team of QA professionals in a complex environment.
Solid experience with Quality Management Systems, audits, and risk‑management tools (FMEA, HAZOP…).
Excellent communication, problem‑solving, prioritization, and cross‑functional influence skills.
Fluency in English and French; ability to work independently, manage conflicts, and drive decision‑making.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Clinical Supply Compliance Expert (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Clinical Supply Compliance Expert who is detail‑driven, solution‑oriented, and collaborative to join our Clinical Supply Chain team, based at our UCB campus located in Braine-l'Alleud, Wallonia, Belgium.

About the role:

In this role, you will play a key part in strengthening the quality and compliance of our global Clinical Supply Chain. You will help ensure that all GMP and non‑GMP operations meet the highest standards, while driving continuous improvement initiatives. You will also guide CSC teams in risk management, documentation excellence, audit readiness, and study support—ultimately helping deliver high‑quality clinical supplies to patients worldwide.

Who you will work with:

You will work closely with colleagues across the Clinical Supply Chain, Quality Assurance, and other cross‑functional partners. You will become a trusted compliance expert, supporting teams in daily operations, regulatory expectations, training activities, and audit preparation. You will be part of a collaborative environment where quality, integrity, and operational excellence are shared commitments.

What you will do:

You will drive and contribute to cross‑functional GMP and compliance initiatives that elevate CSC standards.
You will be responsible for performing gap analyses and implementing effective remediation strategies.
You will manage risk identification, assessment, and mitigation in close collaboration with CSC teams.
You will monitor CSC quality performance metrics and foster a culture of accountability.
You will collaborate with CSC and QA to ensure timely and compliant GMP record management.
You will act as a subject matter expert, promoting best practices in GMP, data integrity, and QMS processes.

Interested? For this role, we are looking for the following education, experience, and skills

Bachelor’s degree (or higher) with at least 5 years’ GMP experience in pharmaceutical quality.
Strong understanding of GMP for investigational medicinal products and related regulatory frameworks.
Solid knowledge of FDA, EU, and ICH guidelines and experience in quality systems (QMS, Veeva a plus).
Highly organized profile with strong analytical ability, communication skills, and attention to detail.
Proven ability to work across teams, lead discussions, and manage workload under pressure.
Fluency in English and French, with strong teamwork mindset and focus on problem solving.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Head Global Suppliers & Materials Quality Management (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

To strengthen our Internal Manufacturing Quality department, we are looking for a talented profile to fill the position of: Head Global Suppliers & Materials Quality Management – Braine l’Alleud, Belgium.

About the role

The Head of Suppliers & Materials Quality Management, is a senior position within the Quality Compliance Operations team, reporting directly to the Head of QA Compliance Operations.

The position focus will be to ensure strategic oversight, harmonization, and continuous improvement across all internal manufacturing sites and strong alignment with External Manufacturing organization, for Suppliers & Materials Quality management that include change notification management, material qualification, quality agreement management, complaints related to suppliers, support of audits schedule and outcome management & general performance of suppliers.

This strategic role ensures that the Suppliers and Materials Qualification across individual operational sites in UCB are implemented in an aligned manner and maintained continuously to meet regulatory requirements and internal corporate standards.

You will work with

Additionally, you will engage with the External Manufacturing organization to align processes. You will also interact with key stakeholders globally across UCB Units to foster a culture of continuous improvement, process optimization and wherever there is a process and value driven digitalization opportunity while supporting the organization’s quality standards.

What you will do

Lead a global quality team who supports operational and strategic activities, provide development opportunities while being value driven.
Lead Gemba sessions across UCB Sites/ Departments to understand existing quality processes part of the role and systems, identify inefficiencies and identify Value Digitalization when needed.
Oversee the implementation and continuous enhancement of Suppliers and Materials Qualification processes, ensuring full alignment with regulatory requirements as well as internal governance and policies.
Drive the global harmonization and standardization of the end‑to‑end supplier qualification lifecycle and material quality oversight, including specifications, monitoring, and quality‑issue trending across internal and manufacturing sites to ensure consistency and compliance globally.

Deploy/ Implement digital supplier‑management solutions to enable advanced data analytics, predictive insights, and proactive risk management.
Support the Head Performance, Operational Excellence in driving Continuous Improvement initiatives aiming on enhancing efficiency, reducing risks, and maintaining high standards of compliance.
Support the Head Audit and Inspection Readiness in managing risks and participating in audits and inspections when required.

Promote a culture of innovation and continuous learning within the team and across the organization.

Serve as the transversal IMQ Single Point Of Contact (SPOC) for Quality Compliance topics below:

Supplier management (quality audits, performance management...)
Change notification management
Material management/ qualification
Quality Agreement for suppliers
Complaints management related to suppliers

Partner with key stakeholders to ensure alignment on quality processes and build regular networking communication (e.g. monthly meeting, monthly gemba...)
Integrate any new IM UCB site into the supplier and materials quality framework by defining a robust strategy and implementing key documentation dedicated to supplier qualification process & material compliance requirements.

Interested? For this position you’ll need the following education, experience and skills

Bachelor’s, master’s degree or an education in a relevant scientific discipline
Minimum of 10 years in Quality Assurance or/and Quality Systems Operations or/and Quality Compliance within a regulated pharmaceutical environment or equivalent
Fluent English communication (oral and written); any additional languages are a plus
Deep understanding of cGMP principles and global regulatory environments
Proven track record in implementing processes dedicated to Suppliers & Materials Quality management (experience in managing SUS, filters is preferred)
Proven track record in leading a team of people across the world
Experience in participating in audits and inspections (FDA)
Experience in Value driven Digitalization is a plus
PMO, green belt, lean & six sigma is a plus
Excellent organizational and analytical abilities to manage projects
Expertise with Suppliers and Materials Quality management: suppliers management (quality audits, performance management), materials quality management, change notification management, quality agreements, complaints management related to suppliers
Exceptional communication and interpersonal skills for effective stakeholder engagement
Strategic thinking with the ability to foster a culture of Quality, Continuous Improvement and Innovation

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

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Artwork & Packaging Development Expert (UK) (Slough, Berkshire, GB)

Data Science Lead 1 (Slough, Berkshire, GB)

Digital Technology Lead - Solution & Programs (Slough, Berkshire, GB)

Non-Clinical Safety Lead - UK (Slough, Berkshire, GB)

Clinical Development Lead (UK) (Slough, Berkshire, GB)

Senior Project Lead Programmer (UK) (Slough, Berkshire, GB)

Senior Real World Evidence Expert (UK) (Slough, Berkshire, GB)

Healthcare & Access Partner - Dermatology - North London (Slough, Berkshire, GB)

Senior Principal Statistician (UK) (Slough, Berkshire, GB)

EU Evidence Generation Lead - Rare Diseases & Epilepsy (Slough, Berkshire, GB)

About the role

Who you’ll work with

What you’ll do

Interested? For this role we’re looking for the following education, experience and skills

Pharmacometrics Team Lead (UK) (Slough, Berkshire, GB)

Clinical Development Lead (Tokyo, Tokyo, JP)

障がい者採用 開発本部 事務職（薬事もしくはオペレーション部） (Tokyo, Tokyo, JP)

主な業務内容について

応募資格・スキル

Principal Statistician (Tokyo, Tokyo, JP)

Patient Access Partner Korea (Seoul, Seoul, KR)

障がい者採用 Medical Strategy Associate（担当疾患領域：てんかん） (Tokyo, Tokyo, JP)

Investigations Lead APAC (Tokyo, Tokyo, JP)

Planning & Execution Lead Immunology (Tokyo, Tokyo, JP)

Supply chain specialist (Hong Kong, Hong Kong, HK)

Rare & Epilepsy Solutions Lead (Seoul, Seoul, KR)

DT Lead CRM & Commercial Solutions Japan (Tokyo, Tokyo, JP)

Medical Solution Lead (Shanghai, Shanghai, CN)

Stagiaire Environnement & Système HSE (Bulle, Gruyere, CH)

Quality Control Microbiology Specialist (Bulle, Gruyere, CH)

Method & Support Trainee (Bulle, Gruyere, CH)

External Manufacturing Operations Lead (Bulle, Gruyere, CH)

Digital Business Analyst Trainee (Bulle, Gruyere, CH)

Laboratory Technician (Bulle, Gruyere, CH)

Technicien·ne de Production Pharmaceutique (Bulle, Gruyere, CH)

Biotech Manufacturing Technician USP (Bulle, Gruyere, CH)

Global SME Clean et Black Utilities (Bulle, Gruyere, CH)

Laboratory Technician (shift 5X8) (Bulle, Gruyere, CH)

MES Engineer (Bulle, Gruyere, CH)

Head Qualification, Validation, Digital and Data Integrity (Switzerland) (Bulle, Gruyere, CH)

Immunology Lead Scandinavia (Stockholm, Stockholm, SE)

Key Account Manager (Field Based, Field Based, CH)

Medical Lead Immunology ECE (Field Based, Field Based, PL)

Non-Clinical Safety Lead - Cambridge, MA (Cambridge, Massachusetts, US)

Content Clearance Lead (Atlanta, Georgia, US)

Account Executive / Scranton, PA (Scranton, Pennsylvania, US)

Account Executive / Scranton, PA Sr/ (Scranton, Pennsylvania, US)

Project Support Assistant (Atlanta, Georgia, US)

Clinical Account Specialist HS - Seattle (Seattle, Washington, US)

Clinical Account Specialist HS - Cleveland (Cleveland, Ohio, US)

Account Executive / Boston (Boston, Massachusetts, US)

Account Executive / Boston Sr. (Boston, Massachusetts, US)

Medical Outcomes Liaison, Central (Dallas, Texas, US)

Medical Outcomes Liaison, Central (Nashville, Tennesee, US)

Head of Reward & Talent Operations US (Atlanta, Georgia, US)

Omnichannel & Digital Marketing Lead - Next Best Action (NBA) (Atlanta, Georgia, US)

Omnichannel & Digital Marketing Lead - Next Best Action (NBA) (Raleigh, North Carolina, US)

Dermatology APP Medical Liaison - East (Field Based, Field Based, US)

Dermatology APP Medical Liaison - West (Field Based, Field Based, US)

Medical Outcomes Liaison, West (Phoenix, Arizona, US)

Medical Outcomes Liaison, West (Seattle, Washington, US)

Learning Manager (Atlanta, Georgia, US)

Medical Science Liaison Dermatology - NYC (New York, New York, US)

Scientist I/II - In Vitro Pharmacology (Cambridge, Massachusetts, US)

Medical Enablement Lead, Atlanta, GA (Atlanta, Georgia, US)

Head of Global RWE and HEOR Strategy - Immunology(ATL) (Atlanta, Georgia, US)

Head of Global RWE and HEOR Strategy - Immunology (BOS) (Boston, Massachusetts, US)

Business Planning & Operations Associate (Atlanta, Georgia, US)

Executive Assistant (Atlanta, Georgia, US)

Competitive Intelligence Lead, Neurology (Atlanta, Georgia, US)

Integrated Insights Lead, US Immunology (Atlanta, Georgia, US)

Scientist I or II - Peptide Chemistry (Cambridge, Massachusetts, US)

Market Project and Process Lead (Atlanta, Georgia, US)

Clinical Account Specialist, Seattle North (Seattle, Washington, US)

障がい者採用開発本部事務職（薬事もしくはオペレーション部） (Tokyo, Tokyo, JP)