Regulatory Jobs
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Director/Senior Director Regulatory CMC
Director / Senior Director Regulatory CMC A clinical stage biotech focused on the development of high-quality therapeutic candidates is seeking a Director / Senior Director Regulatory CMC to join their growing team. This organization is leveraging strong scientific capabilities and a streamlined development approach to drive programs forward. The D...
Senior Vice President Global Regulatory Affairs
A clinical‑stage biotechnology company pioneering next‑generation precision oncology therapeutics is seeking a Vice President/Senior Vice President Global Regulatory Affairs. Their approach is integrating cutting‑edge translational science, advanced patient‑selection methodologies, and a rapidly progressing clinical pipeline with the potential for ...
Boston Scientific Principal Regulatory Affairs Specialist
A leading global medical device company is seeking a Regulatory Affairs Principal to support the review and approval of advertising, promotional, sales, and training materials for its interventional cardiology portfolio. This role applies a risk‑based regulatory mindset to ensure content is accurate, balanced, well‑substantiated, and compliant with...
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Regulatory Specialist
Regulatory Specialist (Contract - W2 Only)Location: Remote (occasional travel within the U.S.) Contract Length: 2 Years Hours: 40 per week Start Date: ASAPAbout the RoleA leading global MedTech client is seeking an experienced Regulatory Specialist to support regulatory strategy and submissions for their orthopaedic device portfolio. This is an exc...
Associate Director, Regulatory Affairs
An innovative biotechnology company is seeking an Associate Director, Regulatory Affairs to serve as a key contributor within its Product Development Team. This individual will play a critical role in shaping regulatory strategy and leading U.S. regulatory submissions that support the advancement of a growing development pipeline. Key Responsibilit...
Regulatory Affairs Consultant (Freelance)
Regulatory Affairs Consultant (Freelance) Location: Brussels, Belgium (hybrid)Length: 12 months (possibility of extension)Start Date: June 2026 Key ResponsibilitiesSupport the development and maintenance of regulatory strategies for new and existing medical device products, including involvement with a Class IIb device.Contribute to regulatory proj...