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:
1. You will drive and contribute to cross‑functional GMP and compliance initiatives that elevate CSC standards.
2. You will be responsible for performing gap analyses and implementing effective remediation strategies.
3. You will manage risk identification, assessment, and mitigation in close collaboration with CSC teams.
4. You will monitor CSC quality performance metrics and foster a culture of accountability.
5. You will collaborate with CSC and QA to ensure timely and compliant GMP record management.
6. 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
7. Bachelor’s degree (or higher) with at least 5 years’ GMP experience in pharmaceutical quality.
8. Strong understanding of GMP for investigational medicinal products and related regulatory frameworks.
9. Solid knowledge of FDA, EU, and ICH guidelines and experience in quality systems (QMS, Veeva a plus).
10. Highly organized profile with strong analytical ability, communication skills, and attention to detail.
11. Proven ability to work across teams, lead discussions, and manage workload under pressure.
12. 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!