17 ago
|
Taevas Life Sciences
|
Bolzano Vicentino
17 ago
Taevas Life Sciences
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. Invii la sua candidatura dopo aver letto i requisiti di competenza e qualifica per questa posizione, riportati di seguito. 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 xrdztoy compliance.
Requires 6-12+ years in medical device regulatory affairs and experience in multi-country
📌 Global Regulatory Affairs Lead - Submissions & Strategy (Bolzano Vicentino)
🏢 Taevas Life Sciences
📍 Bolzano Vicentino