Global Regulatory Affairs Leader – Medical Devices

L7

zimmer biometSan Diego, CAyesterday
Zimmer 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
Apply now

Level

ManagerL7

Location

San Diego, CA

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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