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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...
EHS Engineer (Commissioning)
We are supporting a major pharmaceutical manufacturing facility in Athlone and are looking to speak with experienced EHS professionals to support both ongoing operations and site expansion activities.Key ResponsibilitiesSupport site EHSS programmes and regulatory compliance.Conduct risk assessments, inspections, audits and safety reviews.Support co...
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...
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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...
Regulatory Affairs Specialist
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...
Quality Manager
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...