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...
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...
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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...
A growing medical device company is seeking a Senior Regulatory Affairs Specialist to support global regulatory strategy and submissions across a diverse product portfolio. This role will partner cross-functionally with quality, clinical, and product development teams to ensure compliance with applicable regulations throughout the product lifecycle...
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...