Agilent Technologies is seeking an experienced Regulatory Affairs Specialist to support registrations for new products and renewals across the EMEA region (non-EU). Possiede le competenze, l'esperienza e la determinazione necessarie per avere successo in questo ruolo? Lo scopra qui sotto. 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. xrdztoy #J-*****-Ljbffr Per questa posizione sono disponibili opzioni di lavoro a distanza/a casa.
📌 Global Regulatory Affairs Specialist — Ivd/Devices (Remote) (Milano)
🏢 Altro
📍 Milano