Regulatory & Clinical Strategy Lead - Ophthalmic Devices
ZEISS Meditec Inc.
ZEISS Meditec Inc. in the United States seeks a Senior Advisor of Regulatory and Clinical Affairs to guide regulatory and clinical strategies for CZM's US market, ensuring timely, compliant commercialization of ophthalmic medical devices. You will lead FDA submissions (510(k), PMA, IDE), advise on clinical study design, collaborate with development teams, and represent CZM in FDA meetings and standards bodies. A strong ophthalmology/vision science background and deep FDA experience are required. #J-18808-Ljbffr ZEISS Meditec Inc.
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