Iris Leibovich has extensive experience in quality and validation engineering within the pharmaceutical and medical device industries. From 2011 to 2013, Iris served as a Validation Coordinator at Novetide Ltd., developing validation plans for analytical methods to ensure regulatory compliance. At Taro Pharmaceutical Industries, from 2014 to 2020, Iris worked as a Validation Engineer, where responsibilities included developing validation plans for process equipment and computer systems. Iris transitioned to CooperVision as a Quality Engineer from January 2020 to February 2022, supporting quality management systems and conducting root cause analyses. Currently, Iris holds the position of Design Quality Engineer at Philips, leading design assurance activities and ensuring compliance with quality standards and regulations. Iris has a Bachelor of Science in Biotechnology Engineering from ORT Braude College, a Lead Auditor certification from the Standards Institution of Israel, and a CRA certification from BioForum.
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