Senior Medical Device Regulatory Affairs Specialist
Listed on 2026-10-07
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Pharmaceutical
Medical Science Liaison, Regulatory Compliance Specialist
Viltis is seeking an experienced Senior Regulatory Affairs Specialist to support a leading medical device organization in Alameda, CA. The role focuses on regulatory change assessments and U.S.
medical device submissions, ensuring compliance across product lifecycle. The ideal candidate brings 7+ years of regulatory affairs experience and will partner with Quality, Engineering, Manufacturing, R&D, and Marketing to drive regulatory strategy and timely approvals.
We are currently recruiting a Senior Medical Device Regulatory Affairs Specialist for our team in Alameda, CA, United States.
The position is based in Alameda, CA, United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 120..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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