Global Regulatory Affairs Lead – Submissions

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7fcjj9

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.

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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 xysqume compliance.
Requires 6-12+ years in medical device regulatory affairs and experience in multi-country

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7fcjj9