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Regulatory Specialist
BrusselsNegotiable

Regulatory Affairs Specialist - Medical Devices Location: Belgium (Hybrid)Industry: Medical Devices / Medical Equipment Manufacturing About the Role An established international medical device organisation is seeking a Regulatory Affairs Specialist to support regulatory market access, product lifecycle management, and compliance activities across ...

Regulatory Affairs Manager
DundeeNegotiable

Regulatory Affairs Consultant | ContractContract Details: 📍 Must be based in the UK or Ireland 🏠 Remote 📄 12 Month contract opportunity 🚀 High impact role with significant influence on future regulatory and development strategyAn innovative life sciences organisation is looking for an experienced Regulatory Affairs Consultant to support the dev...

Regulatory Affairs CMC Speciaist
WashingtonNegotiable

Regulatory CMC ConsultantContract: 18 Months Location: Copenhagen, Denmark (Fully Remote) Industry: Vaccines / Global Public HealthWe are supporting a leading pharmaceutical organisation on a high-profile Tuberculosis (TB) vaccine development programme and are looking for an experienced Regulatory CMC Consultant to join the team on an 18-month cont...

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Global Regulatory affairs specialist
WashingtonNegotiable

Principal Regulatory Affairs Opportunity - Global Semaglutide PortfolioWe are supporting a leading global pharmaceutical company in the search for a Principal Regulatory Affairs professional to join a high-profile regulatory team responsible for post-marketing activities across a market-leading chronic disease portfolio.This position offers the opp...

Regulatory Affairs Specialist
Negotiable

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...

Reg affairs
MadridNegotiable

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...