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Regulatory Affairs Specialist

Actalent

Miami, FL, United States Full-time July 11, 2026
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Vacancy Description

Regulatory Affairs Specialist
Location: Miami, FL (Onsite)
Industry: Medical Devices
Experience: 1–3 Years
Education: Bachelor's Degree Required
Join a Growing Medical Device Company Making a Difference
Are you passionate about regulatory compliance, technical documentation, and bringing innovative medical devices to market? We are seeking a detail-oriented Regulatory Affairs Specialist to support regulatory submissions, product registrations, and compliance activities across U.S. and international markets.
In this role, you'll work cross-functionally with Engineering, Quality, Operations, Marketing, and Sales teams to ensure products meet FDA and global regulatory requirements. This is an excellent opportunity for someone early in their Regulatory Affairs career who wants hands-on exposure to FDA submissions, EU Medical Device Regulation (MDR), and global regulatory processes.
What You'll Do

+ Prepare and support regulatory submissions, including FDA 5...

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