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Global Regulatory Affairs Specialist, Medical Devices

Werfen North America, san diego, ca, United States


A medical device company in San Diego is looking for a Regulatory Affairs Manager to oversee compliance with FDA, Health Canada, and EU regulations. The role requires a Bachelor degree and 8 years of experience in regulatory affairs, ideally in the medical device sector. Responsibilities include preparing submissions, reviewing product labeling, and ensuring compliance for product launches. The position offers a salary range of $150,000 - $180,000 annually and may require occasional travel.
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