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Contract Regulatory Jobs

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CMC Submission Lead

CMC Submission Lead | 12-Month Contract | Fully Remote (Europe)We are supporting a global pharmaceutical and biotechnology organisation seeking an experienced CMC Submission Lead to support high-profile regulatory submissions across both development-stage and commercial products.This role will be responsible for leading and coordinating CMC submiss...

CMC Submission Lead
Negotiable

CMC Submission Lead12-Month Contract | Remote (Europe)Pharmaceutical / Biotechnology SectorOverviewWe are supporting a global pharmaceutical and biotechnology organisation seeking an experienced CMC Submission Lead to support a portfolio of regulatory submission activities across development and commercial products.This contract opportunity will pl...

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...

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...

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
BrusselsNegotiable

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...