03 ago
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Taevas Life Sciences
|
Provincia di Vicenza
03 ago
Taevas Life Sciences
Provincia di Vicenza
pTaevas 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. /ppRequires 6-12+ years in medical device regulatory affairs and experience in multi-country /p #J-18808-Ljbffr
📌 Global Regulatory Affairs Lead – Submissions & Strategy (Provincia di Vicenza)
🏢 Taevas Life Sciences
📍 Provincia di Vicenza