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Database & Data Migration Consultant
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...
Indirect Sourcing Manager
Associate Director - Strategic Sourcing & Supplier DevelopmentLocation: Dublin, Ireland (Hybrid - 2 days per week in office) The OpportunityAs Associate Director, Strategic Sourcing & Supplier Development, you will be responsible for leading sourcing initiatives across a spend portfolio of approximately £400M, including £300M of direct spend suppo...
Principal Reg Specialist
Influence Regulatory Strategy for Products That Reach Global MarketsThe OpportunityA global medical device manufacturer is looking for a Regulatory Affairs Specialist to join a well-established regulatory team supporting a diverse product portfolio.This is a role for someone who wants to move beyond transactional regulatory work and become a valued...
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Material Planner
Job Title: Materials Planner (Purchasing) - Contract Location: North Carolina (Onsite, 5 days/week) Contract Length: Initial 6 months (high likelihood of extension) Start Date: ASAPAbout the Role We are working with a leading pharmaceutical company seeking a Materials Planner to support their purchasing and supply chain function. This is a fast-pac...
QA CSV Lead (PAS-X implementation project)
Location: Belgium (40 minutes east of Antwerp)Contract: 6-12 months OverviewWe are seeking a senior QA-CSV professional to provide strategic quality and validation leadership for the implementation of the Next Generation Manufacturing (NGM) PAS|X platform at one of our client's Belgian sites.As the primary QA representative for Computer System Vali...
Regulatory Affairs Specialist
Regulatory Affairs Specialist (Freelance) Location: Lyon, France (hybrid)Length: 12 months (possibility of extension)Hours: Full-time (40 hours per week)Start Date: Mid-August - September 2026Engagement: Freelance Key ResponsibilitiesContribute to the development and maintenance of regulatory strategies for both existing and new medical device pro...