About the role

Bioethic Consulting LLC in San Diego, CA is seeking a Senior Regulatory Affairs Specialist for medical devices to lead regulatory change assessments and U.S. submissions. The ideal candidate has 7+ years of experience in medical device regulatory affairs, with a proven ability to collaborate with Quality, Engineering, Manufacturing, R&D, and Marketing to support product approvals and lifecycle management.

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JOB OVERVIEW

Experience level

Manager

Location

San Diego, CA

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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