Part of Phaidon International
Part of Phaidon International
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Regulatory Affairs Specialist ResponsibilitiesSupport development activities for medical device software products.Develop regulatory strategies and prepare submissions for markets including the United States, European Union, and Canada.Collaborate with regional regulatory teams to align global regulatory strategies.Review and approve product label...
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...