To manage and strengthen relationships with regulatory and government bodies, ensure compliance with licensing and regulatory requirements, WHO-GMP standards for plants and warehouses in the assigned region, and lead Corporate Social Responsibility
Responsible for the preparation of SOPs and laboratory related documents. Handling of sofisticated analytical Instruments and Interpretation of Resulting Data
Key duties include developing IQ/OQ/PQ protocols, managing change controls, handling deviations, training teams, and ensuring data integrity for sterile manufacturing.