You are responsible for ensuring quality by following up and ensuring that processes and actions take place according to the applied GMP quality standards.
Depending on the needs of the project and your expertise, you will work on different tasks.
Main responsibilities
- Deviations, CAPA, Change Control, OOS management;
- Performing PQR (write and review);
- Risk analysis;
- Batch release;
- Implementation and improvement of the QMS;
- Handling and documentation of complaints;
- Supplier management ;
- Prepare and conduct audits.
Requirements
- Master or Bachelor in a life sciences area (pharmacist, bioengineer, chemist, etc.)
- Knowledge of GMP
- A first relevant experience in a QA position
- Fluent in English, excellent command of Dutch or French
- Team player
- Customer oriented
- Flexible
