Quality Systems, Compliance and Excellence Lead
UCB Braine-l’Alleud, Walloon Region, Belgium
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Quality Systems, Compliance and Excellence Lead
UCB Braine-l’Alleud, Walloon Region, Belgium
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Make your mark for patients
We are looking for a Quality Systems Compliance & Excellence Lead who is proactive, collaborative, and quality-driven to join our Clinical Manufacturing Compliance and Excellence Team, based at our UCB campus located in Braine-l’Alleud, Belgium.
About The Role
You will play a key role in ensuring our biologics Pilot Plant operates in full compliance with GMP (and HSE) standards. You’ll be the go-to person for quality systems related to the facility and environment, helping us deliver safe, high-quality drug substances for our patients.
Make your mark for patients
We are looking for a Quality Systems Compliance & Excellence Lead who is proactive, collaborative, and quality-driven to join our Clinical Manufacturing Compliance and Excellence Team, based at our UCB campus located in Braine-l’Alleud, Belgium.
About The Role
You will play a key role in ensuring our biologics Pilot Plant operates in full compliance with GMP (and HSE) standards. You’ll be the go-to person for quality systems related to the facility and environment, helping us deliver safe, high-quality drug substances for our patients.
Who You Will Work With
You’ll collaborate closely with cross-functional teams across Development, Quality, and Manufacturing. You’ll also work hand-in-hand with the Gene Therapy Pilot Plant Environment compliance lead to ensure alignment and mutual support.
What You Will Do
* You will oversee GMP compliance of the facility and environment including being the key contact for the cleaning UCB referent.
* You will be responsible for environmental monitoring (viable and non-viable) and pest control oversight.
* You will manage change controls related to facility/ environment and deviations in case of unexpected environment events.
* You will train staff on facility-related quality systems and GMP standards.
* You will lead monthly quality meetings and drive continuous improvement.
* You will collaborate on GMP training content and risk remediation plans.
For this role, we are looking for the following education, experience, and skills
* Bachelor’s or Master’s degree in sciences with 10+ years in a regulated pharmaceutical environment.
* Strong experience in GMP, environmental monitoring, and quality systems.
* Skilled in managing deviations, change controls, and cross-functional collaboration.
* Proactive mindset with a drive for continuous improvement and lean processes.
* Fluent in French with good English communication skills (written and spoken).
* Autonomous, organized, and team-oriented with strong prioritization skills.
Interested?
Join us in shaping the future of biologics and gene therapy manufacturing at UCB.
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.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Quality Assurance
* Industries
Pharmaceutical Manufacturing
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