Global Regulatory Submissions Lead, Medical Devices
Listed on 2026-10-07
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Healthcare
Healthcare Compliance, Medical Device Industry
Edwards Lifesciences is seeking a Senior Specialist in Regulatory Affairs to join their team in Irvine, CA. This role involves providing regulatory input on product development, overseeing documentation for global submission, and ensuring compliance with regulatory standards. The successful candidate will have at least 5 years of relevant experience and a Bachelor's Degree.
You'll be part of a mission-driven organization focused on improving patients' lives through innovative medical devices. Competitive salaries and extensive benefits programs are available.
We would love to welcome a new Global Regulatory Submissions Lead, Medical Devices to our group in Irvine, CA, United States.
The Global Regulatory Submissions Lead, Medical Devices role at kozmetickesluzby.vecnakraska.sk
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