This is a 9-month position as QA Specialist in a modern and international biotech firm close to Amsterdam. You focus on quality systems and correct entry into those systems.
Job description
As Quality Assurance Specialist in this biotech company, you work GMP documentation from the laboratories and manufacturing site. Your duties are focused on the quality systems itself, so batch record reviewing will not be you primary task. You focus on correct entries in the system, pick up deviations and investigations, and support the teams on quality-related matters. You plan and oversee the issuances of labels and documentation and explain the correct procedures whenever necessary.
Responsibilities
- Collaborate within the QA department
- Oversee quality systems
- Oversee correct labelling and documentation
- Train colleagues in QC and manufacturing
- Reviewlogbooks / label packages and batch documents
Profile
- Bachelor's or master's degree in any field related to biotechnology or pharmaceutical sciences
- 3+ years of experience in a QA position, ideally focused on quality systems
- GMP experience is a hard requirement
Benefits
- Contract: 9 months maternity leave cover, extension uncertain but not excluded
- Salary indication: €4000-5000
- Fulltime position
- Region: Amsterdam
Vacancy number: 22978
