Global Regulatory Affairs Lead — Medical Devices

16 ago - Campo di Ne
Taevas Life Sciences

Taevas Life Sciences in Italy seeks a Global Regulatory Affairs Lead to drive end-to-end product registrations and regulatory strategy across multiple geographies.
La preghiamo di leggere attentamente i seguenti dettagli prima di inviare la sua candidatura.
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.
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Onsite position with global impact.
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