Part of Phaidon International
Part of Phaidon International
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Location: Southern France (exact site location to be discussed)Contract: 3-6 months (extension potential)Working Pattern: Primarily onsiteLanguages: Fluent French requiredOverviewWe are currently seeking experienced GMP Database & Data Migration Consultants to support a major pharmaceutical manufacturing modernization programme. The successful cons...
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...
Freelance Injection Equipment EngineerAssignment OverviewOur client is seeking an experienced Freelance Injection Equipment Engineer to provide specialist engineering support across injection moulding equipment projects within a regulated manufacturing environment. The consultant will work alongside relevant project stakeholders to support the intr...
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Location: Near Toulouse, FranceDuration: Initial 6-12 months (likely to be extended)Start Date: October OverviewWe are supporting a major pharmaceutical manufacturing programme near Toulouse and are seeking experienced MSAT and Pharmaceutical Production Consultants to join a long-term transformation and manufacturing support initiative.The project ...
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...
Regulatory Affairs Specialist (Freelance) Location: Paris, France (hybrid)Length: 12 months (possibility of extension)Hours: Full-time (40 hours per week)Start Date: September 2026Engagement: Freelance Core ResponsibilitiesDesign and implement verification and validation protocols that meet international regulatory standards.Lead the selection and...