Make your mark for patients
We are looking for an Analyst Clinical Bioprocess Analytics who is detail-oriented, proactive, and collaborative to join our Clinical Bioprocess Analytics (CBA) team, based at our UCB campus located in Braine-l’Alleud, Belgium.
About the role
You will ensure operational and analytical activities linked to manufacturing biological Drug Substance for clinical use. You will support multiple campaigns per year, ensuring compliance with GMP and quality standards.
Who you will work with
You will collaborate with a dynamic team based in the Bio Pilot Plant and partner with QA, QC, Development, and external CMOs/CROs to deliver high-quality analytical support.
What you will do
1. You will perform In-Process Control and Monitoring testing during manufacturing campaigns.
2. You will be responsible for delivering accurate analytical data for clinical batches.
3. You will manage analytical operations in production areas, including equipment and troubleshooting.
4. You will contribute to implementing new technologies and improving analytical processes.
5. You will ensure documentation compliance (SOPs, sampling plans, batch records).
6. You will support audits, regulatory submissions, and method transfers.
Interested?
For this role, we are looking for the following education, experience, and skills
7. Bachelor’s degree in Life Sciences or related field.
8. Strong practical experience in analytical techniques (chromatography, ELISA, qPCR, spectroscopy, electrophoresis).
9. Knowledge of GMP standards and quality constraints in QC environments.
10. Proven ability to work under pressure and manage multiple priorities.
11. Excellent organizational, troubleshooting, and interpersonal skills.
12. Flexibility to work shifts, weekends, and bank holidays when required.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!