Jobs at UCB Pharma

Real World Evidence Strategy Lead Solutions (Germany) (Monheim, Mettmann, DE)

Make your mark for patients

We are looking for an Real World Evidence Strategy Lead Solutions who is insight driven, cross functional, and impact focused to join our Real World Evidence team, shaping evidence strategies across UCB’s portfolio. This position can be based in Brussels, Belgium; Slough, UK; Monheim, Germany; Boston, USA; or Atlanta, USA.
About the Role
As RWE Strategy Lead, you will provide strategic leadership for the development and implementation of real world evidence (RWE) and data/registry strategies for assets within a defined disease area. You will ensure that evidence is fit for purpose to meet the needs of multiple stakeholders, including regulators, payers, clinical teams, and patients.
You will work across the full product lifecycle, anticipating evidence needs, aligning stakeholder requirements, and ensuring that RWE supports key decision making and demonstrates the value of UCB’s products. This role requires strong collaboration across functions and the ability to connect evidence generation efforts into a cohesive, impactful strategy.

Who You’ll Work With
You will collaborate closely with teams across global medical, research and clinical development, safety, regulatory, patient engagement, and payer functions. You will also engage with external experts, research partners, and key stakeholders to ensure that RWE strategies are aligned with evolving scientific and policy landscapes.

What You’ll Do
• Define and implement strategic RWE plans to support asset and portfolio needs across stakeholders.
• Design and oversee evidence generation activities, including epidemiology, natural history, comparative effectiveness, and patient centric outcomes.
• Develop data and registry strategies that support regulatory, payer, and clinical decision making.
• Ensure readiness for Joint Clinical Assessment (JCA) and alignment with evolving HTA requirements.
• Lead the execution of RWE studies, ensuring delivery on time, within budget, and to quality standards.
• Collaborate cross functionally to integrate RWE into broader evidence and development strategies.
• Build strong internal and external relationships to drive insight, innovation, and credibility in RWE.
• Translate complex evidence into clear insights to inform strategic decision making.
• Lead, mentor, and develop RWE team members and contribute to capability building across the function.
Interested? For this role we’re looking for:
• Advanced degree in life sciences, epidemiology, health data science, HEOR, or a related field.
• Significant experience in pharmaceutical or healthcare consulting environments, delivering RWE and evidence strategies.
• Strong understanding of how RWE supports decision making across regulatory, payer, and clinical settings.
• Proven ability to work across complex, matrix organisations and influence without direct authority.
• Strong communication, analytical, and leadership skills with a proactive and adaptable 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.

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.

Trainee (m/f/d) Sales Support (Monheim, Mettmann, DE)

We are looking for a Trainee (m/f/d) as a Sales Support who is collaborative, curious, and care-focused to join our Rare and Epilepsy team, based at our UCB office in Monheim am Rhein, Germany.

About the role

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 for 2 years designed to give you a solid start into your career.

You will begin your career in a role where learning, purpose, and real contribution come together. You are going to gain hands-on experience across sales support activities while helping teams create better experiences for patients and the people who care for them. From your first steps, you will build practical knowledge, strengthen your confidence, and discover how human understanding and scientific purpose connect in meaningful everyday work.

Who you will work with

You will join a welcoming team that values encouragement, shared learning, and open collaboration. You are going to work with supportive colleagues across the Rare and Epilepsy team and with internal partners who will help you understand how ideas become action. Experienced team members will guide your development, answer questions, and help you grow your confidence as you contribute to projects, events, and everyday teamwork.

What you will do

support training preparation and coordination for partner-facing processes.
help organize regional and national sales support events.
manage invitations and participate in coordination for meetings and events.
prepare and share sales materials following agreed guidance.
support field administration, expense handling, and event reconciliations.
maintain data and help prepare simple reports and presentations.

Interested?

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

vocational training in business administration expected like Industrial Business Management Assistant or Office Management Assistant, Bachelor’s degree or equivalent experience welcomed
Strong German and good English skills for everyday collaboration.
Confidence using Microsoft Office tools like PowerPoint, expert of using Excel
Curious mindset and enthusiasm for learning through experience.
Strong analytical and numerical skills required for reporting and analysis.
Comfort collaborating across teams and growing through new experiences

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(m/f/d) - Insight to Impact Lead Germany (Monheim, Mettmann, DE)

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Finance Director (m/f/d) – Insight to Impact Lead Germany

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.

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.

Pharmacometrics Team Lead (Germany) (Monheim, Mettmann, DE)

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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.

Logistics & Warehouse Specialist (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Logistics & Warehouse Specialist who is proactive, quality‑driven, and well‑organized to join our Clinical Packaging & logistics Operations team, based at our UCB campus located in Braine‑l’Alleud, Belgium.

About the role:

In this role, you will play a key part in the end‑to‑end operational execution of clinical trial logistics and warehousing activities. You are going to ensure timely, compliant, and accurate distribution of clinical supplies worldwide, supporting trials from Phase 1 to Phase 4. You will work hands‑on with distribution, inventory, and warehouse operations, while collaborating closely with internal and external partners to continuously improve processes and service quality.

Who you will work with:

You will work closely with colleagues across Clinical Supply Chain, Clinical Packaging & Logistics Operations, Quality, and Distribution Compliance teams. You are going to collaborate daily with internal stakeholders, carriers, warehouses, and external partners, building strong relationships to ensure smooth execution of clinical distribution activities.

What you will do :

You will manage end‑to‑end clinical distribution activities, from shipment planning to returns, destruction, and study close‑out.
You will coordinate shipment priorities and ensure timely execution with carriers and internal stakeholders.
You will oversee warehouse operations, including receiving, inventory management, picking, packing, and material dispensing.
You will ensure compliance with GMP, GDP, HSE, and UCB quality standards across all logistics activities.
You will investigate issues, contribute to deviations, procedures, and continuous improvement initiatives.
You will maintain accurate records in SAP ERP, generate reports, and support invoice management.

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

Bachelor’s degree, ideally in logistics, supply chain, or a related field.
Experience in logistics, warehousing, distribution, or production environments.
Strong knowledge of GMP, GDP, and HSE requirements; clinical trial supply experience is a plus.
Good IT skills, with hands‑on experience using SAP ERP in a warehouse or distribution context.
Fluent in English and French, with clear written and verbal communication skills.
Structured, curious, quality‑minded, and comfortable working in a regulated 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.

Head of Digital Technology Data and Architecture (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Head of Digital Technology Data and Architecture who is strategic, collaborative and driven to join us in our Digital Technology Manufacturing and Engineering team, based in our Braine l’Alleud office in Belgium.

About the role

You will play a key leadership role in shaping and delivering the digital data and architecture strategy supporting manufacturing, laboratories and patient supply operations. Working in a global and highly regulated environment, you will define standards, guide transformation programs and ensure secure, integrated and high‑quality data solutions. You will balance strategic vision with practical delivery, lead a talented team, and partner closely with business leaders and technology experts to move the organization forward in an increasingly digital and industrial landscape.

Who you’ll work with

You will be working in a diverse, international team of digital technology, data and architecture professionals, closely connected to manufacturing, laboratories, infrastructure and transformation teams. You will collaborate with senior leaders, internal experts and external partners, gaining access to world‑class knowledge while influencing how digital solutions are designed and adopted across patient supply.

What you’ll do

Define, own and communicate the digital data and architecture strategy for manufacturing, laboratories and patient supply, including roadmaps and standards
Lead and prioritise a portfolio of data and technology initiatives, ensuring delivery on time, on budget and aligned with business value
Drive integration, standardisation and simplification of the digital application landscape across patient supply
Act as a trusted partner to stakeholders, translating business needs into scalable, secure and compliant digital solutions
Lead and develop data and architecture professionals, fostering collaboration, innovation and continuous learning
Ensure high levels of data integrity, cybersecurity awareness and compliance within regulated industrial environments

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

Master’s degree in a relevant field such as information systems, engineering or data‑related disciplines
At least 7 years of experience in digital technology roles within global, regulated manufacturing or industrial environments
Strong background in data strategy, application architecture and complex system integration
Experience leading international programs and managing diverse teams and external partners
Ability to influence, navigate ambiguity and bring people on board around a shared digital vision
Strong understanding of manufacturing, laboratory or supply chain processes and data usage

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 Vendor Lead (Braine L'alleud, Walloon Brabant, BE)

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To strengthen our Global Quality Assurance department, we are looking for a talented profile to fill the position of: Global Quality Auditing Vendor Lead – Braine L’Alleud, Belgium.

About the role
As a Global Quality Auditing Vendor Lead you will be accountable for defining, governing, and continuously improving the global vendor oversight operating model for Global Quality Auditing teams worldwide, with accountability for strategy, performance, compliance, and financial governance across all GxP areas.

You will work with
You will collaborate closely with Global Quality Auditing teams, as well as Finance, Procurement, and other Quality functions. The role also involves regular interaction with cross-functional project teams and senior stakeholders to manage vendors, ensure compliance and drive global process improvements.

What you will do

Auditing Vendor Management & Quality Oversight:

Full ownership of vendor procurement lifecycles: market screening, cross-functional selection, strategic approach, contracting (MSA, SOW), budgeting, PO creation and lifecycle management.
Full financial accountability for the global auditing vendor portfolio, including budget planning, forecasting, cost optimization, vendor contracts, audit activity reporting, and governance updates to Global Quality Auditing and Finance leadership. Compliance monitoring of audit execution, alignment with UCB standards (SOWs, MSA, Procurement & Finance processes).
Definition, harmonization, and monitoring of vendor KPIs, quality indicators, and monthly performance reviews.

Harmonization engine:

Identify improvement needs and implement consistent quality processes and systems across auditing quality units to promote standardization and simplification, thereby enhancing efficiency. Propel positive changes and improvements across the auditing units by enhancing people's skills and processes.

Project Management:

According to the prioritization in alignment with objectives, strategy, and resources allocation for project management activities within GQA; lead, drive or participate to projects within or outside GQA/Quality to improve processes, tools, and operational efficiency.
Drive continuous improvement related to vendor operations, training, and internal auditing processes.

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.
Understanding of business and financial management, and strategic planning.
Demonstrated vendor management experience.
Highly knowledgeable in the global pharmaceutical industry, including the interpretation and application of applicable GxP regulations in complex situations, knowledge of current and future trends in the industry and a deep understanding of major competitors/industry peers.
Ability to manage multiple complex projects at one time, including planning, executing, and monitoring project progress.
Effective written and verbal communication skills for facilitating dialogue across all levels of the organization.
Ability to standardize execution paths across the organization, promoting consistency and efficiency.
Ability to innovate and adapt to changing business 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.

Projects Automation Lead (Braine L'alleud, Walloon Brabant, BE)

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We are looking for a Projects Automation Lead – Engineering who is strategic, collaborative, and delivery‑oriented to join our team based at our UCB campus in Braine‑l’Alleud, Belgium.

About the role

You are going to define and drive UCB’s automation vision across engineering projects and manufacturing sites. You will translate strategic ambitions into a clear multi‑year automation roadmap and ensure its execution through a dedicated automation team. Combining leadership and hands‑on accountability, you will ensure automation solutions are compliant, standardized where needed, and consistently deployed to support long‑term site performance, digitalization, and sustainability.

Who you will work with

You will work closely with engineering project managers, site manufacturing, utilities and facilities teams. You will collaborate with system integrators and suppliers while animating a cross‑site automation network to share best practices, standards, and reusable solutions.

What you will do

You will define and maintain the automation vision, strategy, and multi‑year roadmap for engineering projects and sites.
You will be responsible for building, leading, and developing a central or federated automation team.
You will act as automation discipline owner across capital projects, from concept to handover.
You will ensure automation packages, standards, specifications, and architectures are fit‑for‑purpose and compliant.
You will govern automation initiatives, balancing project delivery with long‑term standardization and sustainability.
You will act as the single point of accountability for automation with internal and external stakeholders.

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

Master’s degree in Engineering (Automation, Electrical, Industrial, Chemical, or similar).
10+ years of experience in industrial automation within regulated manufacturing environments.
Proven experience leading automation teams or disciplines within capital projects.
Strong understanding of automation systems, validation principles, and project lifecycles.
Ability to translate strategy into execution with a pragmatic, delivery‑focused mindset.

Clear and impactful communication skills, translating complex technical topics for diverse audiences.

Excellent stakeholder management and matrix leadership skills.
Fluent in French and English + willing to travel to UK, Switzerland, Japan (20% of the 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.

Impact Quality Lead GVP (Braine L'alleud, Walloon Brabant, BE)

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To strengthen our R&D and Pharmacovigilance Quality department we are looking for a talented profile to fill the position of: Impact Quality Lead – Braine l’Alleud, Belgium

About the role

As Impact Quality Lead you will be part of the with the Impact Quality team within RDPVQ. The Impact Quality Lead is a global role responsible for implementing and maintaining a balanced, proactive, global approach to pharmacovigilance (PV) compliance. This position is primarily responsible for ensuring PV activities are conducted in accordance with applicable global regulatory requirements, guidelines, polices, procedures and industry best practice.

You will work with

You will collaborate closely with UCB cross-functional teams supporting pharmacovigilance activities including the Global Pharmacovigilance organization, Affiliate Offices, Clinical Operations, Regulatory Affairs, Commercial teams, etc. Key responsibilities include overseeing the pharmacovigilance system and pharmacovigilance quality system and providing oversight to Phase IVs studies and post-marketing commitments.

What you will do

Pharmacovigilance System Support

Provides expert guidance on Good Pharmacovigilance Practices (GVP) and Good Clinical Practice (GCP) global regulatory expectations (FDA, EMA, ICH), and industry best practices to ensure compliance and operational excellence.
Provides support to Phase IV study types (i.e. Non-Interventional Studies, Compassionate Use, Surveys, Managed Access Programs, Named Patient Programs, Patient Centered Outcomes Research, Registries).
Provide oversight to UCB patient centric initiatives (including patient support programs, market research programs, digital initiatives, IIS, PASS, medical information, collaboration studies).
Reviews processes for data integrity and quality during signal detection and risk management activities.
Supports validation and control of PV electronic systems.
Ensures PV outputs are compliant including individual case safety reports (ICSRs), development safety update report (DSURs), Risk Management Plan (RMPs), and Risk Evaluation and Mitigation Strategies (REMS), etc.).

PV SOP Management and Training

Provide guidance and support in developing and revising pharmacovigilance SOPs, work instructions, and training materials to ensure regulatory alignment and best practices.
Stay updated on changes in pharmacovigilance regulations, guidelines, and industry trends to ensure ongoing compliance and proactively address emerging requirements.
Ensures targeted training programs on GVP, regulatory expectations, and quality principles are delivered

Partner/Vendor Oversight

Provides critical oversight of PV partners/vendors to ensure efficient, consistent, and compliant pharmacovigilance activities. Monitors contract compliance, quality and timeliness of deliverables.
Interacts with clinical and pharmacovigilance vendors to ensure compliance with GCPs and GVPs and relevant country regulations.

Audits and Inspections

Hosting of PV audits and inspections.
Supports audit and inspection findings by developing and implementing effective remediation plans.

Compliance Monitoring

Leads mitigation efforts with key stakeholders (PV, Safety, Regulatory, and Clinical teams) to ensure alignment on quality standards and compliance requirements.
Monitors regulatory submissions related to on-time delivery of ICSRs (to global Health Authorities, partners, including SUSAR and SAE communication to Ethic Committees and investigators as applicable) as well as the on-time submission of aggregate reports.
Review and monitor vendor compliance through various reports and oversight activities, including tracking KPIs, metrics, and quality control checks.
Participating in Pharmacovigilance specific Governance meetings.
Identifies, tracks, trends, and communicates PV compliance activities to senior management.

Deviation Management and Risk Management

Initiates deviations from discovery, ensures management and root cause analysis, and tracks CAPA implementation, and evaluates effectiveness.
Establishes processes to identify, assess, and mitigate risks related to pharmacovigilance activities.
Collaborate with cross-functional teams to address quality and compliance-related issues and drive process improvement initiatives.

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

Bachelor’s degree, preferably in Science or Engineering.
12+ years of experience in GVP Quality Assurance, GVP Auditing, Pharmacovigilance, or a related field within the pharmaceutical, biotechnology, or healthcare industries.
Fluent English communication (oral and written); any additional languages are a plus.
Proven experience in supporting/leading GVP audits, regulatory inspections, and providing GVP quality management system support.
Strong global knowledge and understanding of local and international regulations applicable to the conduct of clinical trials and pharmacovigilance operations (GVPs, ICH guidelines, FDA, MHRA).
Strong analytical, problem-solving, communication, and decision-making skills.
Strong commitment to ethical standards,
Develops trustful relationships with internal and external stakeholders to accelerate business achievements.
Takes initiatives and works towards delivering results. Takes courageous decisions and balanced risks to create value for patients and UCB.
Ability to anticipate, influence & apply GVP regulations to ensure effective interpretations that support decision-making on current and future solutions to improve patients’ lives.
Ability to independently and critically evaluate quality management systems and quality operations in support of Quality culture and operational output, balancing weaknesses against requirements and expectations.

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.

Documentaliste (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Documentaliste rigoureux·se, méthodique et orienté·e qualité pour rejoindre notre équipe basée sur notre campus UCB à Braine‑l’Alleud, Belgique.

À propos du rôle

Vous allez assurer la gestion et la diffusion des documents contrôlés et des formations du site de Braine au sein des systèmes électroniques UCB (EDMS/LMS), dans le respect des exigences de conformité. Vous jouerez également le rôle d’archiviste du site, en garantissant une gestion rigoureuse des archives papier et en assurant la préparation de documents dans le cadre des audits et inspections.

Avec qui vous allez collaborer

Vous travaillerez en étroite collaboration avec les équipes Qualité, les propriétaires de documents, les formateurs, les line managers et les utilisateurs des systèmes, sur le site de Braine et au sein d’autres entités UCB. Vous serez un point de référence pour la gestion documentaire, les formations et les archives dans un environnement réglementé GxP.

Ce que vous allez faire

Vous allez gérer le cycle de vie complet des documents contrôlés dans le système électronique UCB.
Vous serez responsable des workflows d’approbation, des mises à jour, des revues périodiques et des mises en obsolescence.
Vous assurerez la gestion des formations et des plans de formation dans le système de gestion des formations.
Vous fournirez un support aux utilisateurs des systèmes de gestion documentaire et de formation.
Vous garantirez une classification, une diffusion et un archivage conformes des documents.
Vous gérerez les archives papier et préparerez les dossiers nécessaires aux audits et inspections.

Intéressé·e ?

Pour ce rôle, nous recherchons les compétences et qualifications suivantes

Expérience antérieure en gestion documentaire ou systèmes qualité.
Expérience en gestion électronique des documents et des formations.
Expérience en archivage papier est un atout.
Excellentes capacités d’organisation et de gestion des priorités, notamment en période d’audit.
Esprit d’analyse et rigueur dans l’identification des non‑conformités.
Capacité à travailler en équipe et avec des interlocuteurs variés.
Excellente maîtrise du français et bonne connaissance de l’anglais.

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.

Documentaliste (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Documentaliste rigoureux·se, méthodique et orienté·e qualité pour rejoindre notre équipe basée sur notre campus UCB à Braine‑l’Alleud, Belgique.

À propos du rôle

Avec qui vous allez collaborer

Ce que vous allez faire

Vous allez gérer le cycle de vie complet des documents contrôlés dans le système électronique UCB.
Vous serez responsable des workflows d’approbation, des mises à jour, des revues périodiques et des mises en obsolescence.
Vous assurerez la gestion des formations et des plans de formation dans le système de gestion des formations.
Vous fournirez un support aux utilisateurs des systèmes de gestion documentaire et de formation.
Vous garantirez une classification, une diffusion et un archivage conformes des documents.
Vous gérerez les archives papier et préparerez les dossiers nécessaires aux audits et inspections.

Intéressé·e ?

Pour ce rôle, nous recherchons les compétences et qualifications suivantes

Expérience antérieure en gestion documentaire ou systèmes qualité.
Expérience en gestion électronique des documents et des formations.
Expérience en archivage papier est un atout.
Excellentes capacités d’organisation et de gestion des priorités, notamment en période d’audit.
Esprit d’analyse et rigueur dans l’identification des non‑conformités.
Capacité à travailler en équipe et avec des interlocuteurs variés.
Excellente maîtrise du français et bonne connaissance de l’anglais.

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 ?

Global Laboratory Expert (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Global Laboratory Expert who is strategic, technically strong, and collaborative to join our team, based at our UCB campus located in Braine‑l’Alleud, Belgium.

About the role

You are going to act as the global reference for laboratory equipment and activities at UCB. You will define and drive a global strategy for laboratory Global Technical standards from capital projects to the end of life of a laboratory asset (Physical Asset lifecycle). You will influence design, innovation, and lifecycle management of laboratory assets while supporting project teams and fostering technical excellence across UCB sites worldwide.

Who you will work with

You will collaborate closely with Engineering Project teams, Design Engineering Leads, and Physical Asset Management teams. You are going to work with internal stakeholders across UCB sites as well as external experts, suppliers, and industry networks. You will act as a technical reference and connect to a global network of laboratory scientists and engineering specialists.

What you will do

You will define and drive a global laboratory strategy aligned with engineering, maintenance and business priorities.
You will be responsible for developing technical standards including safety, regulatory, and sustainability aspects.

You will support and manage aspects related to both the laboratory environment and its equipment, including technical specifications, from project phase through to end of life of these assets.

You will ensure compliance with cGxP, pharmacopeia, and engineering standards across all implementations.
You will lead and connect a global network of experts to share best practices and innovations.
You will contribute to technology evolution, innovation, and digitalization in laboratory equipment lifecycle.

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

Master’s degree in engineering or a related technical field.
Strong experience in laboratory equipment and engineering systems within regulated environments.
Knowledge of cGxP, validation (V-cycle, ASTM E2500), and engineering standards.
Good knowledge of different laboratory working environments (e.g. pathogenic, ionizing, radioactive, explosive environments)
Experience in large, complex engineering projects and cross‑functional collaboration.
Ability to interpret needs into solutions, strong communication and stakeholder management skills.
Fluency 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.

Technicien.ne de maintenance (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous cherchons un.e Technicien.ne de Maintenance qui est proactif.ve, rigoureux.se et orienté.e sécurité pour nous rejoindre sur notre campus UCB situé à Braine-l'Alleud, Belgique.

À propos du rôle

En tant que Technicien.ne de Maintenance, vous allez assurer les interventions de maintenance curative et préventive des équipements. Vous serez responsable de l'exécution des travaux de maintenance selon les ordres de travail et les règles GMP.

Avec qui vous allez travailler

Vous allez collaborer avec une équipe de techniciens et d'opérateurs, ainsi qu'avec le responsable maintenance. Vous serez également en contact avec les responsables des opérations chimiques et les services de métrologie.

Ce que vous allez faire

Vous exécutez les travaux de maintenance individuellement ou en équipe, sur des équipements tels que des vannes, pompes, débit mètres, échangeurs, capteurs, …
Vous avez la charge de la documentation des interventions dans le logbook de l'équipement.
Vous préparez les interventions avec les pièces et accessoires nécessaires.
Vous participez à la rédaction et à l'adaptation des instructions de maintenance.
Vous respectez les règles HSE et participer aux analyses de risques.
Vous contribuez à la mise à jour des dossiers techniques et des plans des équipements.

Intéressé.e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes :

Diplôme technique secondaire supérieur avec expérience en maintenance industrielle ou bachelier en électromécanique.
Proactivité, importance de la sécurité et affinités en informatique.
Connaissance des règles GMP et des procédés industriels.
Capacité à travailler en équipe et à communiquer efficacement.
Connaissance des langues : français et anglais technique.
Disponibilité pour participer aux gardes techniques (1 semaine par mois) et ouvert à l’horaire 6-14/14-22.

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 (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

Nous cherchons un.e Technicien.ne de Maintenance qui est proactif.ve, rigoureux.se et orienté.e sécurité pour nous rejoindre sur notre campus UCB situé à Braine-l'Alleud, Belgique.

À propos du rôle

Avec qui vous allez travailler

Ce que vous allez faire

Vous exécutez les travaux de maintenance individuellement ou en équipe, sur des équipements tels que des vannes, pompes, débit mètres, échangeurs, capteurs, …
Vous avez la charge de la documentation des interventions dans le logbook de l'équipement.
Vous préparez les interventions avec les pièces et accessoires nécessaires.
Vous participez à la rédaction et à l'adaptation des instructions de maintenance.
Vous respectez les règles HSE et participer aux analyses de risques.
Vous contribuez à la mise à jour des dossiers techniques et des plans des équipements.

Intéressé.e ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes :

Diplôme technique secondaire supérieur avec expérience en maintenance industrielle ou bachelier en électromécanique.
Proactivité, importance de la sécurité et affinités en informatique.
Connaissance des règles GMP et des procédés industriels.
Capacité à travailler en équipe et à communiquer efficacement.
Connaissance des langues : français et anglais technique.
Disponibilité pour participer aux gardes techniques (1 semaine par mois) et ouvert à l’horaire 6-14/14-22.

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.

QA Systems Officer - Facilities (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a QA Systems Officer (Facilities) who is detail‑oriented, proactive, and quality‑driven to join our team based at our UCB campus in Braine‑l’Alleud, Belgium.

About the role

You are going to ensure that all technical operations related to pharmaceutical production and analysis remain compliant with applicable regulations and UCB Quality Systems. You will co‑develop and implement robust quality systems, maintain a strong state of compliance and control, and proactively drive quality and continuous improvement initiatives. Your role will focus on Quality Management Systems, audit management, access management, pest control, and inspection readiness.

Who you will work with

You will work closely with the manufacturing activities, including the Facilities. You will collaborate with cross‑functional teams to communicate quality systems requirements, support audits and inspections, and foster a strong quality culture across the site.

What you will do

You will maintain and continuously improve the Quality Management System and related processes.
You will organize and coordinate quality oversight on GMP‑compliant pest control across the manufacturing site.
You will support facilities teams with access management, change control, and deviation handling acting as QA.
You will drive continuous improvement initiatives to reduce risk and improve quality KPIs.
You will promote quality culture, compliance awareness, and accountability across UCB teams.

You will support internal and external audits and ensure inspection readiness.

Interested?

For this role, we are looking for the following education, experience, and skills

Master’s degree in a relevant scientific field.
Mandatory experience in Quality in a regulated pharmaceutical or life‑science environment.
Experience with Quality Management Systems and auditing is a strong asset.
Ability to work autonomously, balance multiple priorities, and make fact‑based decisions.
Strong communication, influencing, and stakeholder‑management skills.
Fluency in French and 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 over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Non-Clinical Safety Lead - Belgium (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

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.

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.

QC Technician (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous recherchons un·e Technicien.ne QC qui est rigoureux·se, proactif·ve et doté·e d’un excellent esprit d’équipe pour rejoindre notre équipe Quality Control Analytical Support, basée sur notre campus UCB à Braine‑l’Alleud, Belgique.

À propos du rôle

Vous allez être un pilier analytique essentiel pour garantir des résultats fiables, de qualité et réalisés en toute sécurité. Vous allez analyser les demandes soumises au QC Analytical Support, réaliser les tests analytiques requis et les documenter avec précision. Vous allez également contribuer à la rédaction de protocoles et de rapports analytiques avec l’aide de votre superviseur, tout en veillant à la bonne préparation du laboratoire.

Avec qui vous allez travailler

Vous allez travailler au quotidien avec une équipe laboratoire QC engagée, composée de votre superviseur et de vos collègues analystes. Vous allez collaborer étroitement avec le/la team leader (ou son/sa délégué·e), partager les priorités et assurer la continuité des activités grâce à une forte entraide et une communication fluide.

Ce que vous allez faire

Vous allez analyser les projets soumis au QC Analytical Support et définir les tests nécessaires.
Vous allez documenter fidèlement chaque analyse selon les exigences qualité.
Vous serez responsable de rédiger des protocoles et rapports analytiques avec le support du superviseur.
Vous allez gérer les stocks de produits, réactifs et consommables du laboratoire.
Vous allez mettre en place des actions correctives dans les délais et contribuer à l’amélioration continue.
Vous allez appliquer strictement les règles de sécurité et assurer la suppléance d’autres analystes.

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

Diplôme scientifique (chimie, biochimie, biologie ou équivalent).
Expérience pratique en laboratoire analytique ou en Contrôle Qualité.
Expérience pratique des techniques analytiques suivantes : HPLC, GC, IR, titration, KF/µKF. RMN est un atout.
Excellente rigueur documentaire et sens du détail.
Capacité à travailler selon des procédures validées et des exigences qualité élevées.
Capacité à prioriser, anticiper les besoins et communiquer efficacement.
Esprit d’équipe, sens des responsabilités et culture sécurité forte.

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 ?

QC Technician (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

À propos du rôle

Avec qui vous allez travailler

Ce que vous allez faire

Vous allez analyser les projets soumis au QC Analytical Support et définir les tests nécessaires.
Vous allez documenter fidèlement chaque analyse selon les exigences qualité.
Vous serez responsable de rédiger des protocoles et rapports analytiques avec le support du superviseur.
Vous allez gérer les stocks de produits, réactifs et consommables du laboratoire.
Vous allez mettre en place des actions correctives dans les délais et contribuer à l’amélioration continue.
Vous allez appliquer strictement les règles de sécurité et assurer la suppléance d’autres analystes.

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

Bachelier ou Master scientifique (chimie, biochimie, biologie ou équivalent).
Expérience pratique en laboratoire analytique ou en Contrôle Qualité.
Expérience pratique des techniques analytiques suivantes : HPLC, GC, IR, titration, KF/µKF. RMN est un atout.
Connaissance des outils LIMS et Empower.
Excellente rigueur documentaire et sens du détail.
Capacité à travailler selon des procédures validées et des exigences qualité élevées.
Capacité à prioriser, anticiper les besoins et communiquer efficacement.
Esprit d’équipe, sens des responsabilités et culture sécurité forte.

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 ?

Senior Scientist - Injectable Drug Product Process Development (Braine L'alleud, Walloon Brabant, BE)

Make your mark for patients

We are looking for a Senior Scientist – Injectable Drug Product Process Development who is curious, collaborative, and solution-oriented to join our Drug Product Process Development team, based in Braine-l’Alleud offices, in Belgium.

About the role
You will play a key role in developing safe, high-quality injectable medicines (biologics and gene therapy) for clinical studies and future patients. You will design, develop, and improve drug product manufacturing processes, from early studies through to late-stage development. Working at laboratory scale and alongside manufacturing teams, you will contribute your technical expertise to ensure robust, compliant, and scalable injectable drug products.

Who you’ll work with
You will be working in a multidisciplinary team of scientists, engineers, and manufacturing specialists. You will collaborate closely with internal development and manufacturing teams, as well as external partners, to define and deliver drug product processes that support clinical and commercial needs.

What you’ll do

Design, develop, and optimize injectable drug product manufacturing processes for clinical and late-stage development.
Plan and execute laboratory studies, analyze data, and document results in reports and development documentation.
Support the manufacture of clinical and stability batches in collaboration with manufacturing teams and partners.
Perform process risk assessments and contribute to process understanding and continuous improvement.
Contribute to regulatory documentation and respond to health authority questions related to drug product development.
Support investigations related to product quality and contribute to effective knowledge transfer across teams.

Interested?

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

Advanced degree in pharmaceutical sciences, chemistry, biotechnology, or a related scientific discipline.
At least 8 years of experience in sterile liquid injectable drug product development or manufacturing within the biopharmaceutical industry.
Hands-on knowledge of aseptic manufacturing processes for injectable products such as vials or pre-filled devices.
Solid experience in monoclonal antibodies and/or gene therapy products (rAAV is a plus).
Strong problem-solving skills with the ability to analyze data and propose practical, compliant solutions.
Ability to work collaboratively across teams and communicate clearly with both internal and external partners.

# GeneTherapy

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.

Maintenance Technician (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous cherchons un Technicien de Maintenance, curieux et proactif pour rejoindre notre équipe de Production, basée dans notre campus UCB, à Braine-L'Alleud, Belgique.

À propos du rôle

Vous serez responsable du réglage et de l'entretien de notre parc machine, impliquant des connaissances avancées en électromécanique. Votre rôle consistera à assurer le bon fonctionnement et la longévité de nos équipements grâce à une maintenance régulière et des réparations rapides.

Le rôle s’effectue à 100% sur site et comprend des horaires en shift, du lundi au vendredi (6h-14h et 14h-22h).

Avec qui vous allez travailler

Vous allez collaborer étroitement avec le Team Leader et les autres membres de l'équipe pour assurer le bon fonctionnement de nos lignes de production. Notre équipe valorise la coopération, le respect et l'amélioration continue.

Ce que vous allez faire

Effectuer les changements de formats et démarrer les équipements.
Entretenir et réparer les équipements, diagnostiquer les pannes rapidement.
Établir et mettre en œuvre des calendriers de maintenance préventive.
Analyser les incidents et effectuer la maintenance curative.
Consigner toutes les interventions et problèmes dans SAP PM/OT et les Batch Cards.
Participer au Tier meetings en tant que représentant technique

Intéressé ? Pour ce rôle, nous recherchons la formation, l'expérience et les compétences suivantes

Connaissances avancées en électromécanique.
Expérience en maintenance et réparation d'équipements.
Maîtrise de SAP PM/OT.
Compétences analytiques et de résolution de problèmes.
Capacité à travailler en équipe de manière collaborative.

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 ?

Opérateur Zone Aseptique (CDD de 6 mois) (Braine L'alleud, Walloon Brabant, BE)

Faites la différence pour les patients

Nous cherchons un(e) Opérateur(trice) de Production Aseptique qui est passionné(e), méticuleux(se) et autonome pour nous rejoindre dans notre équipe de production, basée dans notre campus UCB situé à Braine-l-Alleud.

À propos du rôle :

Vous serez responsable d'assurer la qualité et la continuité de la production injectable, en nettoyant les sas d'accès en zone B, en réceptionnant et approvisionnant la zone aseptique en équipements et matériels stériles, et en effectuant diverses opérations de maintenance et de contrôle.

Avec qui vous allez travailler :

Vous ferez partie d'une équipe dynamique et collaborative, où votre contribution sera essentielle à la réussite collective de nos opérations de production.

Ce que vous allez faire :

· Vous allez effectuer les opérations pour garantir la qualité et la continuité de la production injectable.

· Vous serez responsable du nettoyage des sas d'accès en zone B.

· Vous gérerez la réception et l'approvisionnement de la zone aseptique en équipements et matériels stériles.

· Vous veillerez à l'ordre, à la propreté et à la gestion des déchets dans la zone aseptique.

· Vous contrôlerez le nettoyage et vérifierez le statut des équipements et locaux de la zone de production aseptique.

· Vous déchargerez l'autoclave de stérilisation du matériel et contrôlerez le matériel de production après la stérilisation avant de le stocker en zone aseptique.

· Vous effectuerez le monitoring d'environnement selon les procédures en vigueur.

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

· Diplôme d'études secondaires et de préférence une expérience antérieure dans un rôle similaire.

· Connaissance des normes de sécurité et des bonnes pratiques de fabrication.

· Capacité à travailler de manière autonome et en équipe.