pAgilent invites an experienced Regulatory Affairs Specialist to join our Global Regulatory Affairs team, coordinating international submissions primarily for the EMEA (non-EU) region. You will manage regulatory blocks, use the GTS tool, and collaborate with global teams to ensure timely registrations and renewals of IVD products across hardware, software, and immunochemistry. /ppThis role offers an opportunity to impact product lifecycle and compliance while working in a highly collaborative /p #J-18808-Ljbffr
📌 Global IVD Regulatory Affairs Specialist (Remote) (Italia)
🏢 Agilent
📍 Italia
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