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. xlwpduy
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This role offers an opportunity to impact product lifecycle and compliance while working in a highly collaborative
Per questa posizione sono disponibili opzioni di lavoro da remoto/a casa.
📌 Global IVD Regulatory Affairs Specialist (Remote) (Roma)
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📍 Roma