Basic requirements:
1. Higher education (preference is given to candidates with a master's degree, scientific degree or scientific title);
2. At least 2 years of experience in the field;
3. Excellent knowledge of the state language (possession of international certificates in foreign languages ​​​​gives an advantage);
4. Ability to use information and communication technologies in practice, have practical knowledge of MS Office, Microsoft Excel.
Additional requirements:
1. Control the activities of the Center in the field of discipline of implementation of laws and regulatory documents and form, analyze, generalize the database on implementation and provide methodological guidance in the field of organizational control and analysis of them;
2. Experience in developing government resolutions, regulatory legal acts in accordance with the requirements of the necessary practices (GxP) and working with them.

Main requirements:
1. Must have a higher education and scientific degree in the field of pharmacy (preference is given to candidates with a Master's degree, Candidate of Sciences, PhD Doctor of Philosophy);
2. Have at least 3 years of experience in the field of pharmacy;
3. Have certificates of compliance with the requirements of national standards of Good Practices (GxP);
4. Excellent knowledge of the state language (possession of international certificates in foreign languages ​​​​gives priority);
5. Be able to apply information and communication technologies in practice, have practical knowledge of MS Office, Microsoft Excel.

Additional requirements:
1. Organize research and development work to further introduce innovative technologies into the production process of medicines, medical devices and medical equipment;
2. Have a deep understanding of the essence of the reforms being carried out in the country regarding the requirements of Good Practices (GxP);
3. Must have experience in developing and working with government regulations, regulatory documents, and good practice (GCP) requirements.

Main requirements:
1. Higher education (in the field of information and communication technologies);
2. Excellent knowledge of the state language (possession of international certificates in foreign languages ​​​​gives an advantage);
3. Knowledge of information and communication technologies, excellent knowledge of MS Office, Microsoft Excel, Microsoft Windows Server, Linux operating systems, practical knowledge of MS Office.
Additional requirements:
1. Preference is given to persons with work experience.

Basic requirements:
1. Higher education (in pharmacy, medicine, chemical biology and chemical technology);
2. At least 2 years of experience in the pharmaceutical field;
3. Excellent knowledge of the state language (possession of international certificates in foreign languages ​​​​gives an advantage);
4. Ability to use information and communication technologies in practice, practical knowledge of MS Office, Microsoft Excel.
Additional requirements:
1. Deep understanding of the essence of the reforms being carried out in the country regarding Good Practices (GPP) requirements;
2. Experience in developing and working with government resolutions, regulatory legal acts on Good Practices (GPP) requirements.

Main requirements:
1. Must have a higher education and scientific degree in the field of pharmacy (preference is given to candidates with a Master's degree, Candidate of Sciences, PhD Doctor of Philosophy);
2. At least 5 years of experience in the field of pharmacy, of which at least 2 years in a managerial position (in a state organization);
3. Certificates of compliance with the requirements of national standards of necessary practices (GxP);
4. Excellent knowledge of the state language (possession of international certificates in foreign languages ​​​​gives priority);
5. Ability to apply information and communication technologies in practice, practical knowledge of MS Office, Microsoft Excel.

Additional requirements:
1. Organization of research and development work to further introduce innovative technologies into the production process of medicines, medical devices and medical equipment;
2. Have a deep understanding of the essence of the reforms being carried out in the country regarding the requirements of Good Practices (GPP);
3. Have experience in developing and working with government resolutions, regulatory legal acts regarding the requirements of Good Practices (GPP).