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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...
Field Service Engineer
Freelance Contract | Ditta Individuale / Libero Professionista | August 2026 - December 2026 Contract Details Start Date: August 2026End Date: December 2026Location: ItalyContract Type: Freelance / ContractWorking Pattern: Approximately 40 hours per weekTravel: Travel required, including flights, hotels, trains, and driving between customer sitesEx...
Continued Process Verification Consultant
Location: Anagni, ScoppitoContract length: 9-10 monthsNumber of positions: 6OverviewWe are supporting the implementation of a global Continued Process Verification (CPV) programme across pharmaceutical manufacturing sites in Italy. Consultants will play a key role in establishing site-level CPV strategies aligned with standardised global guidance ...
