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
📌 Global Regulatory Affairs Lead – Submissions (Provincia di Vicenza)
🏢 Taevas Life Sciences
📍 Provincia di Vicenza
Candidati a questo annuncio
Mostra le tue capacità professionali all'azienda, compila il form e lascia un tocco personale nella lettera di presentazione, aiuterà il recruiter nella scelta del candidato.