Eti Zinger has over 25 years of experience in the medical device industry, demonstrating a strong commitment to quality and compliance. They have held various roles, including Quality Assurance Manager and Regulatory Affairs Associate, and currently serve as the Director of Regulatory Affairs and Quality Assurance at Endospan Ltd., where they lead regulatory submissions and maintain robust quality systems. Eti has a proven track record in ensuring ISO 13485 and FDA compliance, driving sustainable growth, and enhancing patient safety through strategic collaboration. They hold an M.A. in Cognitive Sciences from The Hebrew University of Jerusalem and a B.A. in Multi-disciplinary Arts from Tel Aviv University.
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