We are seeking an experienced QC Lab Equipment Validation Engineer to support a major pharmaceutical project based in the Netherlands. This is an exciting opportunity to join a high-performing validation team on a fast-paced site, ensuring laboratory equipment is compliant, qualified, and audit-ready.
Key Responsibilities:
- Execute and support qualification activities (IQ/OQ/PQ) for QC laboratory equipment
- Develop and review validation documentation including protocols, reports, and risk assessments
- Ensure compliance with GMP, GxP, and regulatory requirements (e.g., EMA, FDA)
- Perform gap assessments and support remediation activities
- Collaborate with cross-functional teams including QA, QC, Engineering, and external vendors
- Support audits and inspections as required
- Maintain accurate documentation in line with data integrity standards (ALCOA+)
Equipment Scope (desirable experience):
- HPLC / UPLC systems
- GC systems
- Dissolution testers
- UV/Vis spectrophotometers
- TOC analyzers
- Balances and general lab instrumentation
Requirements:
- Degree in Engineering, Life Sciences, or related discipline
- Proven experience in QC equipment validation within pharmaceutical or biotech environments
- Strong knowledge of GMP and regulatory standards
- Experience with validation lifecycle documentation
- Excellent communication and stakeholder management skills
- Ability to work independently in a project-driven environment
Darwin Recruitment is acting as an Employment Business in relation to this vacancy.
Greg King