Iris Shamir

Iris Shamir has extensive work experience in the pharmaceutical and medical devices industry. Iris'smost recent role was as the VP of the Pharmaceutical Quality Section at Gsap, starting in June 2023. Prior to that, they worked as a QA Manager at EZbra from January 2023 to June 2023.

From October 2020 to January 2023, Iris worked as a GMP Inspector at the Ministry of Health Israel. Before that, they were the Global QA/RA Director for Medical Devices at Q Medical Devices, a Q Company, from October 2019 to October 2020.

Iris also held a position as the Director of Quality Assurance for Medical Devices at Q Holding Company from July 2018 to October 2020. Iris has previous experience at Teva Pharmaceuticals, where they served as the Kfar Saba Site Quality Head from November 2016 to February 2018, the Jerusalem Site Quality Head from November 2013 to November 2016, and the Head of Compliance for IL Pharma sites from February 2012 to October 2013.

Iris started their career at Dexcel Pharma in 1998, where they held various roles including GxP Compliance Manager from July 2006 to February 2012, Laboratory Team Leader from December 1999 to June 2006, and Laboratory Analyst from November 1998 to November 1999.

Iris Shamir completed their Bachelor of Science degree in Food Engineering and Biotechnology at Technion - Israel Institute of Technology from 1986 to 1990. Following that, they pursued a Master of Science degree in Biochemistry and Nutrition at The Hebrew University of Jerusalem from 1990 to 1992.