01 ago
|
Altro
|
Campo di Ne
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-*****-Ljbffr
📌 Global Regulatory Affairs Lead - Submissions & Strategy (Campo di Ne)
🏢 Altro
📍 Campo di Ne