Part of Phaidon International
Part of Phaidon International
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Senior Regulatory Affairs SpecialistIrvine, CA (Hybrid)$100,000 - $120,000 Job DescriptionEPM Scientific is partnered with an established medical device innovator developing life-changing technologies that address critical patient needs in the cardiovascular and interventional space. As the company continues to expand its global footprint, they are...
Regulatory Affairs SpecialistMedical Device / Pharma | Hybrid Opportunity | Competitive Salary + BenefitsAre you a Regulatory Affairs professional looking for an opportunity to make a real impact on innovative products that improve patient outcomes?A growing healthcare organisation is seeking a Regulatory Affairs Specialist to join its expanding te...
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...
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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...
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...