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

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