Compliance Jobs
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QA Manager Biologics
This is a 6‑month contract position based in Leiden, The Netherlands, requiring a minimum on‑site presence of 4 days per week. The Quality Assurance Manager will play a key role in ensuring compliance with EU GMP standards and supporting biologics production in an aseptic/sterile manufacturing environment. Fluency in Dutch (spoken and written) is ...
Sterilisation Validation
The Consultant will lead and support sterilisation strategy, validation, and compliance activities across the full lifecycle of medical devices, including Class IIa. The role requires deep expertise in sterilisation modalities, microbiological testing, and regulatory frameworks under both FDA and EU MDR. Job Title: Sterilisation ValidationDuration:...
Validation and Verification Engineer
About the Role:We are seeking a Verification & Validation (V&V) Engineer to ensure compliance and process integrity for medical devices involving neutron activation technologies. This role focuses on validating complex processes within a regulated environment, ensuring adherence to international standards and supporting product performance requirem...
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QA auditors
We are supporting a major GMP readiness programme across several manufacturing and QC sites in Leiden and Amsterdam. To strengthen inspection preparedness, we are assembling a team of experienced Quality Consultants who can perform daily mock audits, identify gaps, and ensure each site is fully prepared for upcoming regulatory inspections. Dutch la...
Technical Engineer (QC Lab)
We are seeking a Technical Engineer (QC) with a strong GMP background to support laboratory operations and facility systems. This role is critical to ensuring equipment reliability, compliance, and smooth day-to-day functioning in a regulated environment. The ideal candidate is hands-on, technically skilled, and fluent in Dutch, as most documentati...
Post-Market Surveillance Consultant
Post‑Market Surveillance Consultant (Medical Devices)Location: Eindhoven, Netherlands Contract length: 12 months Engagement: Freelance / ContractKey ResponsibilitiesLead and execute Post‑Market Surveillance activities in compliance with EU MDR 2017/745.Develop, maintain, and update PMS documentation, including:PMS PlansPMS Reports (PMSR)Periodic Sa...
