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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 xrdztoy compliance. Vuole candidarsi? Legga tutte le informazioni su questa posizione qui sotto, poi prema il pulsante per candidarsi. 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)
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