Part of Phaidon International![]()
Showing 36 results
Sort by:
Head of Regulatory Affairs (m/f/d)About the opportunity This is a chance to shape regulatory strategy, not just follow the rules. You'll take ownership of the Regulatory Affairs function at a well-established global manufacturer. You'll lead the team, build a global regulatory structure, and play a key part in keeping the business compliant as regu...
Director / Senior Director, Regulatory Strategy Clinical-stage biotech | San Francisco Bay Area | HybridWe're partnering with an innovative clinical-stage biotech that is advancing novel biologic therapies in areas of high unmet need. As the pipeline progresses through the clinic, the company is looking for a strategic, hands-on regulatory leader t...
Head of Regulatory Affairs Clinical-stage biotech | Flexible / Remote (US)We're partnering with an innovative clinical-stage biotech developing novel therapies in areas of significant unmet medical need. As early programs move into the clinic, the company is looking for a hands-on regulatory leader to own strategy from the ground up.The opportunity...
Take the first step toward your next opportunity - submit your CV and get started today.

Global Head of Regulatory Affairs A global biopharmaceutical company is seeking Head of Global Regulatory Strategy to lead regulatory strategy for a high-profile injectable aesthetics portfolio. This individual will provide strategic leadership across both biologic and medical device products, with primary responsibility for neurotoxin programs and...
Global Regulatory Strategy Lead About the OpportunityA global specialty biopharmaceutical company focused on innovative dermatology therapies is seeking an experienced Global Regulatory Affairs Lead to drive worldwide regulatory strategy for a late-stage/marketed biologic across multiple indications. This individual will lead global regulatory plan...
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...