pAgilent 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. /ppYou 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. /p #J-18808-Ljbffr
📌 EMEA Regulatory Affairs Lead – IVD/Medical Devices (Milano)
🏢 Agilent
📍 Milano
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