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
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📌 Global Regulatory Affairs Lead – Submissions & Strategy (Campo di Ne)
🏢 Taevas Life Sciences
📍 Campo di Ne
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