About the role

Abbott seeks a Principal Regulatory Affairs Specialist to join the Vascular Division on-site in Temecula, CA or Santa Clara, CA. You will provide regulatory leadership for a portfolio of endovascular medical devices and guide global regulatory strategies throughout the product lifecycle. The role requires preparing FDA submissions (510(k)/PMA), EU MDR activities, and close collaboration with Regulatory Operations, Quality, Clinical, R&D, Manufacturing, and Marketing to ensure compliant, timely

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JOB OVERVIEW

Experience level

Manager

Location

Temecula, CA

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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