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 ...
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...
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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...
Associate Director, Regulatory Affairs
Our client is a globally established science‑focused company supporting end‑to‑end development and manufacturing for healthcare and technology partners. They are currently looking for an Associate Director of Regulatory Affairs to lead regulatory strategy, oversee key submissions, and serve as a trusted partner to internal and external stakeholders...
Regulatory Specialist
Regulatory Affairs Specialist (12‑Month Contract)Focus: 510(k) FDA Submission - Cardiology Medical DevicesOverviewWe are seeking an experienced Regulatory Affairs Specialist to support the preparation, execution, and submission of a 510(k) premarket notification for an innovative cardiology medical device. This is a 12‑month contract role with resp...