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...
CQV Consultant (Contract)Location: Lyon Region, France (On-site) Contract Length: 12 Months Industry: Pharmaceuticals Start Date: ASAPThe OpportunityWe are supporting a leading pharmaceutical manufacturing site undergoing a significant capital investment and expansion programme. As part of this project, we are seeking an experienced CQV Consultant ...
Data Integrity & CSV Program ManagerLocation: Lyon, France Start: Approximately 1-2 months Duration: 12 months Language: Fluent French requiredRole OverviewWe are seeking an experienced Data Integrity & CSV Program Manager to lead a large-scale Data Integrity programme within a pharmaceutical manufacturing environment.The programme will involve the...
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Position: Product Manager - Ruminant Specialisation (M/F)Permanent Contract (CDI) - Based in Brittany, FranceYour RoleReporting to the Technical & Marketing Manager, you will be responsible for providing technical expertise to the global team and managing the ruminant product portfolio.Key ResponsibilitiesTechnical SupportProvide species-specific t...
Location: Lyon, France (Hybrid) Contract Length: 12 Months Start Date: Mid-October 2026 Engagement: Freelance We're supporting an established medical technology organisation developing innovative drug delivery and combination products. They are seeking an experienced Regulatory Affairs & Quality Consultant to lead key regulatory and quality initia...
Key ResponsibilitiesSupport and execute process and technology transfer activities for sterile drug products.Prepare, review, and author GMP-compliant technical documentation and transfer packages.Evaluate manufacturing processes, equipment suitability, process performance data, and facility readiness.Review deviations, investigations, CAPAs, proce...