Agilent Technologies is seeking an experienced Regulatory Affairs Specialist to support registrations for new products and renewals across the EMEA region (non-EU).
You will coordinate international submissions, manage regulatory blocks, and collaborate with Global Regulatory Affairs to ensure timely registrations of IVD and medical device products, including hardware, software and immunochemistry technologies.
J-18808-Ljbffr
📌 Global Regulatory Affairs Specialist — IVD/Devices (Italia)
🏢 Altro
📍 Italia
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