Contract Quality Specialist Jobs
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Scientist
Standort: Visp, Schweiz Vertragsdauer: 01. Februar 2026 - 31. Januar 2027 Homeoffice: Möglich (hybrides Modell)Wir unterstützen ein führendes Unternehmen im pharmazeutischen Sektor bei der Suche nach einer/m Wissenschaftler/in für das Team in Visp, Schweiz. Diese Position bietet die Möglichkeit, an hochrelevanten Projekten in einem cGMP-konformen U...
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:...
Quality inspector
Location: Multiple production sites, France (6 sites of interest)Duration: 4-6 months (contract)Start Date: Monday, 22nd December (no work required on 25th December) Shifts:Option A: 12-hour shifts (day/night)Option B: 8-hour shifts (morning/evening/night) Payment Structure:Day shift - standard day rateEvening shift - 1.25x day rateNight shift - ...
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Quality Assurance Consultant
Quality Assurance Consultant - Medical Equipment Manufacturing (Berlin 🇩🇪)An opportunity to support a leading medical‑device manufacturer in Berlin on a high‑impact Quality Assurance assignment. This project focuses on strengthening compliance, product reliability, and documentation excellence across a portfolio of Class III cardiovascular implan...
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...
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...