Part of Phaidon InternationalProperty 1 Bull Dark

Sie befinden sich auf der Webseite für Deutschland [DE]. , um die Länderseite anzuzeigen, die mit Ihren Browsereinstellungen verknüpft ist

Regulatory Jobs

Showing 5 results

Sort by:

Head of Regulatory Affairs (m/f/d)
£130,000 - £150,000 GBP a year

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 Affairs
Jersey City$213,000 - $288,000 USD a year

We are seeking an experienced regulatory leader to provide strategic and operational regulatory support across late-stage oncology programs. This individual will play a critical role in shaping global regulatory strategy, leading health authority interactions, and driving major regulatory submissions from development through registration. Dependin...

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...

Senior Regulatory Affairs Specialist
IrvineNegotiable

Senior Regulatory Affairs Specialist Overview Join a growing neurovascular medical device team supporting regulatory compliance and product lifecycle activities for innovative technologies used to treat stroke and other neurovascular conditions. This onsite position (4 days/week) partners closely with engineering, quality, clinical, and commercial ...

Regulatory Affairs Specialist
Los AngelesNegotiable

Regulatory Affairs Specialist ResponsibilitiesSupport development activities for medical device software products.Develop regulatory strategies and prepare submissions for markets including the United States, European Union, and Canada.Collaborate with regional regulatory teams to align global regulatory strategies.Review and approve product label...