Part of Phaidon International![]()
Showing 8 results
Sort by:
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...
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...
Take the first step toward your next opportunity - submit your CV and get started today.

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...
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...