Dr. Guzikevich is an organic chemist with more than 15 years of experience in the pharmaceutical industry. She earned her doctoral degree in structural biology and chemistry at the Weizmann Institute of Science and has authored three peer-reviewed publications in Nature. Dr. Guzikevich is an expert in Quality Assurance and Regulatory Affairs, and has profound knowledge in international pharmaceutical guidelines, including standards of Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP).
Dr. Guzikevich has successfully led dozens of FDA, European, Israeli, and other Health Authorities Inspections. She has played leading roles at major pharmaceutical firms, including Quality Assurance of commercial GMP facilities, Quality Control laboratories, development manufacturing plants, and Research & Development laboratories. Gali was the Global GMP QA Senior Director at Teva Pharmaceuticals for 8 years. Prior to that role, she served as the Director of Quality and Regulatory Affairs at Teva Pharmaceuticals. Gali also worked as a Product Manager for Agan Chemical Manufacturers.
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