Global Regulatory Affairs Director — Medical Devices
Listed on 2026-10-06
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Healthcare
Healthcare Management -
Management
Healthcare Management
Spryte Medical, LLC. is seeking an experienced Director of Regulatory Affairs to lead global regulatory strategies for a portfolio of innovative medical devices.
You will partner with executives and cross‑functional teams to drive timely approvals and market access while building a scalable regulatory function. Responsibilities include leading complex submissions (IDE, De Novo, PMA, 510(k), EU MDR), managing regulatory agency interactions, and shaping regulatory processes for growth.
Join us at Spryte Medical, LLC. as our next Global Regulatory Affairs Director — Medical Devices in Bedford, MA, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Global Regulatory Affairs Director — Medical Devices role in the description above.
We appreciate your interest in this position.
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