Global Regulatory Affairs Leader – Medical Devices
zimmer biometSan Diego, CA
Global Regulatory Affairs Leader – Medical Devices
L7
zimmer biometSan Diego, CAyesterday
Industries
Electromedical and Electrotherapeutic Apparatus ManufacturingSurgical and Medical Instrument ManufacturingSurgical Appliance and Supplies ManufacturingZimmer Biomet, a global medical technology leader, seeks a Regulatory Affairs professional to develop and execute regulatory strategies that ensure FDA compliance and meet international requirements. You will author filings (510(k)s, Letters to File, IDEs, technical documentation) and maintain SOPs, while liaising with FDA, notified bodies, and other agencies across the product lifecycle.
Required:
minimum 8 years of regulatory affairs experience in medical devices, international experience; RAC
Apply now
Level
ManagerL7
Location
San Diego, CA
Occupation
Regulatory Affairs Managers
Industry
Electromedical and Electrotherapeutic Apparatus Manufacturing
Posted
yesterday
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