Taevas Life Sciences in Italy seeks a Global Regulatory Affairs Lead to drive end-to-end product registrations and regulatory strategy across multiple geographies. You will ensure compliance with country-specific requirements and timely market entry for Taevas products.
The role requires leadership in regulatory submissions (US FDA, CE/MDR, CDSCO) and strong coordination with international partners, labs, and regulatory consultants. Onsite position with global impact.
📌 Global Regulatory Affairs Lead — Medical Devices (Monteviale)
🏢 Taevas Life Sciences
📍 Monteviale
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