15 ago
|
Altro
|
Bolzano Vicentino
15 ago
Altro
Bolzano Vicentino
Taevas Life Sciences in Italy seeks a Global Regulatory Affairs Lead responsible for end-to-end product registrations and regulatory strategy across multiple geographies, driving timely market entry. You will lead regulatory submissions (US FDA, CE/MDR, CDSCO, etc.), manage technical documentation, track approvals, and liaise with agencies and partners to ensure labeling, UDI and packaging compliance.
Requires 6-12+ years in medical device regulatory affairs and experience in multi-country
J-18808-Ljbffr
📌 Global Regulatory Affairs Lead – Submissions (Bolzano Vicentino)
🏢 Altro
📍 Bolzano Vicentino