Part of Phaidon International
Part of Phaidon International
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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...
I'm currently looking for a CMC Regulatory Affairs Specialist with strong experience in late-stage development, EU regulatory submissions, and vaccines/biologics products, with a particular focus on tuberculosis (TB) vaccines. Candidates with broader public health vaccine experience in biologics environments will also be considered, but vaccine exp...
I'm currently looking for a CMC Regulatory Affairs Specialist with strong experience in late-stage development, EU regulatory submissions, and vaccines/biologics products, with a particular focus on tuberculosis (TB) vaccines. Candidates with broader public health vaccine experience in biologics environments will also be considered, but vaccine exp...
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I'm currently looking for a CMC Regulatory Affairs Specialist with strong experience in late-stage development, EU regulatory submissions, and vaccines/biologics products, with a particular focus on tuberculosis (TB) vaccines. Candidates with broader public health vaccine experience in biologics environments will also be considered, but vaccine exp...
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...
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...