- N-nitrosamines risk assessments in finished drug products in accordance with EMA and FDA guidelines;

- reports on the polymorphism study (XRPD, DSC) of the active pharmaceutical ingredients both in pure form and in finished drugs;

- reports on the validation and transfer of analytical methods of quality control of finished drug products;

- reports on the compatibility of components in the finished drug products;

- preparation of tables with the stability results of finished drug products;

- accounting and circulation of developed drugs under their stability studies;

- contract management and business correspondence with company partners;

- purchase of equipment, reagents and consumables for R&D Department of company;

- accounting and circulation of reagents, consumables and reference substances in R&D Department of company.

- systematization and analysis of scientific information from various sources (articles, patents, abstracts, Internet resources);

- design of the idea, novelty and practice application of the research;

- development of experiment plan covered synthesis and study of catalysts (predominantly inorganic materials) by adsorption and spectral techniques;

- technical processing and analysis of the obtained experimental data;- preparing articles and patents, oral and poster presentations at the conferences.

- systematization and analysis of scientific information from various sources (articles, patents, abstracts, Internet resources);

- design of the idea, novelty and practice application of the research;

- development of experiment plan covered synthesis and study of catalysts (predominantly inorganic materials) by adsorption and spectral techniques;

- technical processing and analysis of the obtained experimental data;

- preparing articles and patents, oral and poster presentations at the conferences.

Practical course of General and Inorganic Chemistry, supervision of Master students.