Total work experience in the pharmaceutical industry: 15 years.
Education: Saint-Petersburg State Chemical-Pharmaceutical Academy, faculty of industrial drug technology.
Professional career: I have started my professional way in pharmaceutical industry in 2007 as a process operator/shift leader at the manufacturing site producing active pharmaceutical ingredients by chemical synthesis. From 2008 to 2013, I have been working at the Federal State Research Institute of Highly Pure Biopharmaceuticals (Saint-Petersburg) as a validation/process engineer. During 2013-2014 I worked in the city of Kaluga at the Novo Nordisk insulin plant dealing with aseptic production and environmental monitoring.
In 2014, I began working in the newly created Russian State GMP inspectorate in FSI "SID &GP" (Moscow) as a senior inspector.
At the beginning of 2017, I took the position of Deputy Head of the Inspection Department of the FSI "SID &GP". During the period from 2014 to 2019, I have conducted more than 80 GMP inspections in Russia and overseas, most of them as a lead inspector.
During 2017-2019 I also held the position of Deputy Head of the Educational Center for Good Practices of the FSI "SID and GP" dealing with training programs for Russian GMP inspectors and also for other regulatory authorities of the Eurasian Economic Union.
Since 2018, I have been a member of the Steering Committee of the Eurasian Union ISPE Affiliate, and in 2019 I headed it.
Currently, I am the Chair of the Eurasian Union ISPE Affiliate (ISPE EAEU). Besides that, I also provide some consulting services in the area of the GM(D)P compliance for Eurasian and foreign pharmaceutical companies.