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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:...

About the JobA global, innovation‑driven specialty chemicals company is a leading provider of polyurethane solutions for the automotive and industrial sectors, supporting OEMs and Tier suppliers worldwide. With a strong focus on sustainability, advanced materials, and market‑driven innovation. Your RoleLead strategic marketing activities for the au...

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 (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...

EPM is currently partnered with a trusted client of over 4 years that is currently seeking to embed a freelance program manager within their team to support them on one of their leading accounts.Below you can find the details of the role highlightedContract Criteria:3-Month Initial Engagement (Potential to extend)40 hours per week80% Remote (with l...