We are looking for a Quality Officer that is responsible for ensuring GMP-compliance on the production floor in this international biotech firm in Amsterdam. You oversee all GMP-documentation from production, and are present on the floor to audit the work, logbooks, and daily activities.
Job Description
You are part of the production team as a Quality Officer and review all documentation before it is sent to the QA-department. Together with QA, you perform investigations, implement changes, execute CAPA's, and ensure the production team is following GMP-procedures properly. You perform internal audits, host external audits, and represent the production team in internal meetings. Since you are so closely involved with all quality aspects in the production department, you are in a key position to identify, shape, and execute improvement projects. In short, you are the key person to ensure GMP-compliance on the production floor, giving you a very broad, dynamic, and involved role as Quality Officer.
Responsibilities
- Batch Record Review, production records
- Execute investigations, changes, and corrective actions
- Check the work on the floor, check logbooks
- Perform internal audits, host external audits
- Identify and execute improvements
- Represent the production department internally
Profile
- Bachelor or Master in a relevant field (biotech, chemistry, pharmaceutical sciences etc)
- Very strong background in GMP
- Experience with executing investigations and implementing changes
- English is a hard requirement, Dutch is a small plus
Benefits and practical information
- Long term position, contract provided directly by our client
- Salary range: €5000,- to €7000,- gross monthly
- Fulltime position, flexibility in working hours, occasional work from home is possible
- Location: Amsterdam
- Vacaturenummer: 24464
