Part of Phaidon International
Part of Phaidon International
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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...
EPM Scientific is supporting a Global MedTech to hire a Sr. RA Consultant to join their Joint Replacement RA Team, looking for someone with a strong background in EU & US regulations, ideally with Orthopaedics & Sustaining/Change Control experience.This is a 12 month, 4 days per week, remote hourly rate contract, start dates ideally mid-September.J...
Copilot said: CMC Regulatory Affairs SpecialistLocation: Copenhagen, Denmark Contract: 6 Months Initial Contract (Extension Likely) Start Date: September 2026We are supporting an innovative pharmaceutical company in Copenhagen seeking a CMC Regulatory Affairs Specialist to support a key late-stage development programme.This is an excellent oppor...
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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...
Job Title: Regulatory Affairs SpecialistDuration: 12 months (with extension opportunity)Hours: Full-time (hybrid/remote)Location: Paris, France Core ResponsibilitiesDesign and implement verification and validation protocols that meet international regulatory standards.Lead the selection and approval of testing partners under global certification sc...