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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...
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...
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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 Manager
Regulatory Affairs Manager | Medical Devices & Combination ProductsAn innovative healthcare start up is seeking a senior Regulatory Affairs professional to join the business during a critical growth phase. With multiple products progressing through development and commercialisation, this is an opportunity to build and lead the regulatory function w...
Regulatory Affairs Manager
Regulatory Affairs Manager | Medical Devices & Combination ProductsAn innovative healthcare start up is seeking a senior Regulatory Affairs professional to join the business during a critical growth phase. With multiple products progressing through development and commercialisation, this is an opportunity to build and lead the regulatory function w...