Senior Regulatory Affairs Manager – Medical Devices; Hybrid, CA)
Listed on 2026-10-11
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Healthcare
Healthcare Management
Neuro Pace, based in Mountain View, CA, seeks a Senior Regulatory Affairs Manager to lead regulatory support for new product development, sustaining, and clinical study projects for a fully implantable US Class III medical device system. This hybrid role requires involvement 2-3 days in the Mountain View office.
You will supervise regulatory staff, drive submissions (PMA/IDE), and ensure compliance across lifecycle, partnering with clinical affairs, biocompatibility, software, and cybersecurity
Step into the Senior Regulatory Affairs Manager – Medical Devices (Hybrid, CA) role at Neuro Pace in Mountain View, CA, United States and grow with us.
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 Senior Regulatory Affairs Manager – Medical Devices (Hybrid, CA) role in the description above.
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