We are looking for a Validation Engineer for a biotech firm near Amsterdam. You create and execute protocols for a nice mix between practical- and office work. Read on below and apply today!
Job description
You have a broad role focused on validation, qualification and commissioning activities, both in the office and hands-on. You create and execute protocols for Validation and Qualification (CQ, IQ, OQ, and PQ) for equipment, facilities and Computerized systems (CSV). You take part in investigations and consecutive CAPA implementation. You review other GMP-documentation, such as SOPs, test records, reports and protocols. You work with internal colleagues to establish and enforce strategies and procedure and with external parties for calibrations and certifications. We are looking for someone with 5+ years of GMP-experience and demonstrable Validation experience.
Responsibilities
- Create and execute commissioning, validation and qualification protocols
- Temperature mapping
- Investigations and CAPA implementation
- Coordinate calibration and certification
- Review GMP-documents
- Risk assessments
Profile
- MLO4 or HBO background
- 5+ years of GMP-experience
- Experience with Validation and Qualification
- Unlimited work visa to work in The Netherlands
Benefits
- Contract through Oxford
- Fulltime position
- 1 year contract, extension possible but not guaranteed
- Salary range: €5000,- to €5600,- per month
- Location: Amsterdam area
- Vacaturenummer: 26972
