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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...

Senior Regulatory Affairs Specialist
San Francisco$120,000 USD a year

Senior Regulatory Affairs SpecialistWe're hiring a Senior Regulatory Affairs Specialist to support U.S. and global regulatory submissions for medical devices and partner with cross-functional teams to ensure regulatory compliance throughout the product lifecycle.Key ResponsibilitiesPrepare and support submissions including IDEs, 510(k)s, CE Technic...

Regualtory Affairs Specialist
$70,000 - $90,000 USD a year

Regulatory Affairs SpecialistMedical Device / Pharma | Hybrid Opportunity | Competitive Salary + BenefitsAre you a Regulatory Affairs professional looking for an opportunity to make a real impact on innovative products that improve patient outcomes?A growing healthcare organisation is seeking a Regulatory Affairs Specialist to join its expanding te...

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Selby Jennings Start Your Career In Recruitment
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...

Senior Specialist, Regulatory Affairs
SummitNegotiable

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...

Principal Specialist, Regulatory Affairs
SummitNegotiable

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 ...