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...
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 ...
Field Service engineer - France / Spain Start Date: August 2026End Date: December 2026Location: Open to candidates based anywhere in EuropeContract Type: Freelance / ContractWorking Pattern: Approximately 40 hours per weekTravel: Extensive European travel required, including flights, hotels, trains, and driving between customer sitesExpenses: Trave...
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OverviewWe are seeking an experienced Process Engineer to support validation activities within a regulated medical device manufacturing environment. The successful candidate will play a key role in ensuring manufacturing processes are validated, compliant, and capable of consistently producing high-quality products.Key ResponsibilitiesLead and supp...
EPM Scientific are currently supporting a Medical Device client in Southern Ireland to hire a Sr. Project Engineer on an NPI project, working on a long term (18-24 month) contract. Full time on site, starting in September.Job details:Drive process development, optimization, and cost reduction initiatives across the business units.Take full ownershi...
We are currently partnering with a leading global bio-pharmaceutical manufacturer looking to hire a EMR Maintenance Engineer professional in one of their major sites in Switzerland. This person will support calibration, maintenance, and compliance activities within a GMP-regulated manufacturing environment.Key Responsibilities:Prepare, execute, and...