About the role

Venus Concept in New York, NY invites a Vice President of Regulatory Affairs, Quality Assurance & Quality Control to lead global regulatory and quality strategies. You will ensure safety, compliance, and product excellence across the organization. This executive role requires 10+ years in medical device regulatory affairs/QA, including at least 3 years at VP level, with experience in FDA submissions, EU MDR, risk management, and leading audits and inspections.

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JOB OVERVIEW

Experience level

Manager

Location

New York, NY

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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