Global Regulatory Affairs Specialist — IVD/Devices

13 ago - Milano
Agilent Technologies

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.

Farmacista Lucca

17 ago - Toscana
Medi - Market Italia

Farmacista Lucca

17 ago - Toscana
Medi - Market Italia

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