Developing and ensuring compliance with quality plans and programs
Coordinating regulatory inspections under the manufacturing and wholesale distribution licenses
Implementing regulatory compliance in cooperation with the Regulatory Affairs Manager
Monitoring of Group quality standards and their implementation in the local QMS
Recording and initial assessment of reported cases of drug risks or suspected cases where pharmaceutical-technical defects are involved
Collaboration and point of contact for Customer Service/KAMs/Medical Information and other departments regarding complaints.
Zentiva is a pharmaceutical company focused on manufacturing and wholesale distribution of drugs. The company operates under regulated manufacturing and wholesale distribution licenses and maintains robust quality management systems (QMS) across its operations. Zentiva is dedicated to ensuring pharmaceutical compliance, safety, and quality standards throughout its product lifecycle, including monitoring drug risks and managing customer complaints related to pharmaceutical-technical defects. The company collaborates across multiple departments including Regulatory Affairs, Customer Service, Medical Information, and Key Account Managers to maintain the highest standards of pharmaceutical excellence.
