EMEA Regulatory Affairs Lead – IVD/Medical Devices

Agilent in Milan, Italy, is seeking a Sr. International Regulatory Affairs Specialist to coordinate submissions across the EMEA region for IVD/medical device products, including hardware, software, and immunochemistry technologies. You will manage daily regulatory blocks, use the GTS tool, and collaborate with Global Regulatory Affairs to ensure timely registrations and renewals, while overseeing channel partner licenses and renewals.

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