Compliance Jobs
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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:...
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...
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Qualification Engineer Sterile Fill‑Finish On‑Site Utrecht
This short‑term contract position requires a Dutch‑speaking Qualification Engineer who can work fully on‑site in Utrecht/Bilthoven to support the qualification of a sterile fill‑finish production line. The role focuses on delivering compliant, inspection‑ready qualification of equipment, cleanrooms, utilities, and monitoring systems in accordance w...
Quality MDR Specialist
Role DetailsContract: 12 monthsLocation: Ile-de-France, France - Hybrid (around 80% onsite presence required)Start date: ASAPLanguages: French (required) & Professional English Key ResponsibilitiesSupport the ongoing MDR transition within the Quality teamLead or contribute to risk assessments aligned with MDR requirementsProvide expert guidance on ...
Senior CQV Specialists
A major global pharmaceutical company is building a new state‑of‑the‑art facility in France, covering aseptic manufacturing and high‑performance clean utilities. To support the commissioning, qualification, and validation (CQV) program, the client is seeking experienced CQV Consultants with strong technical depth and the ability to operate in a Fre...