Global Regulatory Affairs Lead, Medical Devices

L7

envistaMahwah, NJyesterday
Versah, LLC, now part of the Envista family, seeks a Regulatory Affairs leader to develop global strategies and maintain regulatory approvals for its medical device portfolio. You will collaborate with R&D, Engineering, Quality, Operations, Marketing, and Sales to support product lifecycle activities. The role emphasizes compliance with 21 CFR 820, ISO 13485, and EU MDR, while guiding audits and regulatory interactions across markets.
Apply now
Apply now

Level

ManagerL7

Location

Mahwah, NJ

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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