Agilent 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.
This role offers an opportunity to impact product lifecycle and compliance while working in a highly collaborative
📌 Global IVD Regulatory Affairs Specialist (Remote) (Roma)
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📍 Roma
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