Amir Levinger

Amir Levinger is an experienced professional in quality assurance and regulatory affairs within the medical device sector. Currently serving as an Active Medical Device Auditor at Kiwa Dare since 2022, Amir is responsible for compliance assessments and certification recommendations related to ISO 13485 and MDR. Previously, Amir held the position of QA & RA Manager at Notal Vision and CORDIO Medical Ltd., focusing on regulatory compliance and quality management system implementation. Prior roles include QA Compliance Lead and Senior Quality Assurance Engineer at West Pharmaceutical Services, along with engineering positions at companies like 3M and Hospitech Respiration Ltd. Amir completed a Bachelor of Science in Biomedical Engineering at Ben-Gurion University of the Negev from 2001 to 2005.