Management of the CC1 supporting team in the Quality Operations Department. Motivating employees and supporting them with substantive knowledge and expertise in the field of regulatory provisions. To assist Quality Operations Head in developing, implementing and supervising the operation of the Quality Management System in the Quality Operations Department. Participation in the preparation of Polpharma Biologics S.A. for pharmaceutical inspections and audits carried out by domestic and foreign regulatory authorities. Ensuring the correct conduct of processes for which the Quality Operations Department is responsible, including the batch documentation assessment process.