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
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
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...
Senior Specialist, Regulatory Affairs
About the JobA growing commercial-stage biotechnology company focused on advancing innovative therapies in oncology and immunology is seeking a Senior Specialist, Health Authorities to support global clinical regulatory strategy and submission activities for investigational and marketed products. This individual will play a key role in preparing re...
Senior Specialist Regulatory Affairs
Senior Specialist, Regulatory AffairsAbout the Job A growing commercial-stage biotechnology company focused on advancing innovative therapies in oncology and immunology is seeking a Senior Specialist, Health Authorities to support global clinical regulatory strategy and submission activities for investigational and marketed products. This individua...
Principal Specialist, Regulatory Affairs
A growing biotechnology company is seeking a Principal Specialist, Regulatory Affairs (Health Authorities) to support global regulatory strategy and health authority submissions for investigational and marketed products. This role will partner closely with Clinical, Regulatory, and cross-functional teams to advance development programs and support ...