Treace is seeking a Principal Regulatory Affairs Specialist to lead regulatory activities for software devices (SaMD/SiMD) in a fast-growing medical device environment. You will collaborate with Product Development, Quality, Operations, Marketing, and Legal to ensure timely submissions and compliant labeling. The role emphasizes mentorship, process improvement, and staying ahead of regulatory changes. A strong track record in US FDA submissions and international registrations is essential.

Also on the board Same function, level within a rung

Level

Manager

Location

Ponte Vedra Beach, FL

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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