Regulatory Affairs Strategist: FDA/IVDR; Medical Devices
Listed on 2026-10-09
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Healthcare
Healthcare Compliance, Medical Science Liaison -
Pharmaceutical
Healthcare Compliance, Medical Science Liaison
Natera is seeking a senior Regulatory Affairs professional to lead the regulatory function on cross-functional teams and interact with authorities on FDA Pharma and EU IVDR programs.
You will build and execute bold regulatory strategies and coordinate submissions, including EU IVDR Technical Documentation and 510(k) premarket notifications, to enable timely product approvals and market access.
The following opening is for a Regulatory Affairs Strategist: FDA/IVDR (Medical Devices) with Natera.
We are looking to fill the Regulatory Affairs Strategist: FDA/IVDR (Medical Devices) position at Natera in United States.
The Regulatory Affairs Strategist: FDA/IVDR (Medical Devices) role at Natera is now open for applications in United States.
Join us at Natera as our next Regulatory Affairs Strategist: FDA/IVDR (Medical Devices) in United States.
We are currently recruiting a Regulatory Affairs Strategist: FDA/IVDR (Medical Devices) for our team in United States.
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