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We are supporting a leading medical device manufacturer seeking an experienced Validation Engineer to support equipment qualification and manufacturing validation activities across a regulated production environment.This role will play a key part in delivering validation projects for new and existing manufacturing equipment, ensuring compliance wit...
Validation Engineer Location: Lyon, France (hybrid)Start date: September 2026Hours: Full-timeContract length: 12 months - freelance In this role, you will contribute to the qualification and validation of manufacturing processes, equipment, and products throughout the product lifecycle. Working closely with internal teams and external partners, you...
Quality Manager - FREELANCE CONTRACT Contract DetailsStart Date: ImmediatelyLocation: Montpellier, France (3 days on-site/2 days remote)Hours: 40 hours per week (full-time)Engagement: Freelance Key ResponsibilitiesEnsure the Quality Management System remains compliant with internal procedures and applicable global regulatory requirements, includin...
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Metrology Quality Engineer (12-Month Contract)📍 France | 🏥 Medical Device ManufacturingWe are supporting a leading medical device manufacturer in their search for an experienced Metrology Quality Engineer to join their site on an initial 12-month contract.This is a high-impact role focused on establishing and developing an on-site Metrology and ...
Location: Toulouse Area, France Contract: Freelance / Consulting Assignment Industry: Pharmaceutical Manufacturing / CDMO Start: Q3/Q4 2026The ProjectWe are supporting a major pharmaceutical manufacturing site in the Toulouse area that is undergoing significant expansion and operational growth.Multiple projects are running simultaneously across m...
Contract DetailsStart Date: ImmediatelyLocation: Montpellier, France (5 days on-site)Hours: 40 hours per week (full-time)Engagement: 6 month Freelance Contract Key ResponsibilitiesEnsure the Quality Management System remains compliant with internal procedures and applicable global regulatory requirements, including ISO 13485, EU MDR, FDA QSR/QMSR, ...