Senior Process Quality Specialist 1

Make your mark for patients

We are looking for a Process Quality Excellence Specialist who is detail-oriented, collaborative, and proactive to join us in our Global Clinical Sciences and Operations team, based in our office in Slough, UK; Brussels, Belgium; or Monheim, Germany.

About the role

You will be working in a team that ensures the highest standards of quality and compliance in clinical studies. Your focus will be on developing, maintaining, and improving clinical quality systems and procedures, ensuring that risks are identified and mitigated in line with international regulations and best practices.

Who you’ll work with

You will be working in a diverse, global team that collaborates closely with colleagues in Quality, Patient Safety, Regulatory Affairs, and strategic partners. Together, you will drive and continuous improvement across Global Clinical Sciences and Operations.

What you’ll do

• Support the development and maintenance of quality and compliance infrastructure, including policies, procedures, and best practices.
• Collaborate with cross-functional teams to ensure compliance with international regulations.
• Lead and coordinate audit planning and execution.
• Provide guidance on quality standards and regulatory requirements to team members.
• Identify and mitigate compliance risks, escalating critical issues as needed.
• Contribute to continuous improvement initiatives and share industry trends and best practices.

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

• Bachelor’s degree or higher in a relevant field (e.g., life sciences, pharmacy, medicine, or law).
• Or significant experience in the pharmaceutical industry, preferably in quality management or clinical development.
• In-depth knowledge of international clinical quality standards and regulatory guidelines.
• Strong analytical, problem-solving, and project management skills.
• Excellent communication and interpersonal skills, with fluency in English.
• Experience in writing and maintaining standard operating procedures is essential.

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. 

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. 

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.