Make your mark for patients
We are looking for a Clinical Manufacturing Process Engineer who is innovative, detail-oriented, and collaborative to join our Clinical Manufacturing team, based at our UCB campus located in Braine-l'Alleud, Belgium.
About the role
You are going to play a key role in shaping the future of biologics and gene therapy at UCB. You will be responsible for implementing and transferring clinical manufacturing processes for our next-generation biological and gene therapy products, ensuring they are ready for commercialization.
Who you will work with
You will join a passionate and cross-functional Clinical Manufacturing (CM) team, working closely with process development, quality, and commercial stakeholders. You’ll collaborate with experts across UCB to bring innovative therapies to life.
What you will do
1. You will implement manufacturing processes in clinical plants and ensure GMP readiness.
2. You will be responsible for on-floor support during clinical manufacturing campaigns.
3. You will manage upstream technology transfers to commercial manufacturing sites.
4. You will collaborate with stakeholders to support process industrialization.
5. You will analyze batch data to enhance process knowledge and drive improvements.
6. You will represent Clinical Manufacturing in cross-functional and regulatory discussions.
Interested?
For this role, we are looking for the following education, experience, and skills:
7. You hold a Master’s degree in a scientific or engineering discipline.
8. You bring at least 5 years of experience in biologics and/or ATMP manufacturing.
9. You have hands-on expertise in upstream processes and scale-up.
10. You are experienced in GMP compliance and equipment qualification.
11. You have led CAPEX or CMC development projects successfully.
12. You are fluent in both French and English, with strong communication skills.
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!