GMP Compliance
Contracting – Brabant Wallon
Your responsibilities:
The incumbent will provide support to the QA operational team in production building by:
- Being present in the production area to conduct gembas, housekeeping, and oversight.
- Providing support in managing the QA Ops technician team
- Reviewing and approving documentation as a quality partner, or provide support during reviews.
Your profile:
- A university certificate with scientific orientation (Bio engineer, Biology, Biotechnology, Pharmacology,…) or equivalent experience.
- Good knowledge of English (oral and written) & fluent in French
- 3 years’ experience in cGMP environment
- Knowledge of regulatory matters and Good Manufacturing Practices (GMP).
- Analytical and critical mind, global and pragmatic approach, problem solving.
- Good impact and influence skills as well as networking skills to efficiently work within different Vaccine departments.
- Good technical writing skills.
Our offer ?
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply or send me your CV, [email protected]