We are looking for a QA Officer for a biotech firm in Hoofddorp. You review complete batch records for completeness and compliance with cGMP quality guidelines.
Job description
About 70% of your time is focused on batch record review in this role. Other duties are administration-related tasks such as archiving and preparing binders. The batch records you review are for therapies for individual patients and contain Manufacturing- and Quality Control data. You prepare the records for release by the QP and have a large responsibilities in recognizing and reporting deviations or values that are out of the specifications. We are looking for someone with some batch record review experience in a QA-department. This is a relatively junior position and candidates with a master's degree will not be considered.
Responsibilities
- Batch Record Review
- Check Production records
- Review QC-data
- Review Environmental Monitoring information
- Identify and report deviations
- Archiving and preparing binders
Profile
- MBO or HBO degree in a relevant field (quality, biotech, pharma, etc)
- 2-3 years of QA Experience
- Experience in biotech is a plus
- You have an unlimited work permit for the EU
Benefits and practical information
- Position until the end of 2025, extension possible
- First contract provided by Oxford Global Resources
- Occasional weekend work required according to set schedule
- Fulltime position
- Salary range: €4000 - €4500,- gross per month plus holiday allowance.
- Location: Hoofddorp
- Vacaturenummer: 25785
