Global Regulatory Affairs Specialist – Medical Devices; TMTT
Listed on 2026-10-10
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Healthcare
Healthcare Compliance, Medical Science Liaison
Edwards is seeking a Regulatory Affairs professional to guide complex domestic and international product submissions within the Transcatheter Mitral and Tricuspid Therapies portfolio. You will partner with EW affiliates and cross-functional teams to ensure timely, compliant filings and align with global regulations.
The role requires a Bachelor's degree with at least five years of related experience and a solid understanding of regulatory requirements for medical devices.
Our organisation is growing, and we are hiring a Global Regulatory Affairs Specialist – Medical Devices (TMTT) in Irvine, CA, United States.
This is a strong role to take on the Global Regulatory Affairs Specialist – Medical Devices (TMTT) role at Edwards.
As a Global Regulatory Affairs Specialist – Medical Devices (TMTT), you will play an important part at Edwards in Irvine, CA, United States.
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