Permanent Regulatory Jobs
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Director / Senior Director Regulatory Affairs
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
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...
Head of Regulatory Affairs (m/f/d)
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...
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Sr. Director of Regulatory Affairs
Job Title: Senior Director of Regulatory AffairsReports to: Chief Medical OfficerJob OverviewThe Senior Director of Regulatory Affairs will provide strategic and operational leadership for regulatory affairs activities supporting an in vitro diagnostic (IVD) and laboratory developed test (LDT) product portfolio, including tests/assays intended for ...
Senior Regulatory Affairs Specialist
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
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...