Description
Our Global biopharmaceutical client in the Netherlands is looking for a QA Officer to join their project team for an exceptional contract opportunity.As the QA Officer you will represent QA in the project team, this means that you will be the first person to decide that project decisions are acceptable from a Quality point of view, or that escalation is needed.
Responsibilities
- Project overview: facilities upgrades, equipment modification or new equipment, and process validation related to these activities.
- QA review (and in some cases approval) of all qualification/validation related documentation.
Requirements:
- Dutch Speaking, English will be an advantage.
- Strong experience working in a GMP manufacturing environment.
- In depth knowledge of Quality / acting as the QA responsible for review and approvals of documentation – URS / IQ / OQ / PQ.
- Experience of CAPA’S, Document Control and review / action of Deviations.
- Team-oriented, flexible and can work independently.