Regulatory Jobs
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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...
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 ...
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...
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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...
Regulatory Affairs Specialist (Autónomo)
Regulatory Affairs Specialist (Autónomo) - Medical Devices Location: Madrid, Spain (remote - 1 day per month travel)Length: 9 months (possibility of extension)Start Date: ASAP We are partnered with a growing medical device manufacturer seeking an experienced Regulatory Affairs Specialist (Autónomo contractor) for a 9‑month engagement. This is an ur...
CMC Regulatory Affairs Consultant
Do you want to be a driving force in a rapidly expanding environment, making a tangible difference in the process? Our Client a global leading Consultancy firm is looking for a CMC Regulatory Affairs person Tasks Provide clients with expert guidance on quality-related considerations throughout drug development, working closely with internal special...