01Managing the entire QA activities in the plant & Overall implementation of Quality Systems in all units.02Design, Develop and approve all Quality systems in all units. Monitoring, Documentation, and implementation of process development.03Responsible to handle regulatory audits USFDA ISO 9001-14001, EU,WHO, and their compliance in all units without any Major Non Compliance.Making sure that there is stability data to support retest or expiry dates and storage conditions on APIs and/or intermediates where appropriate; and Performing product quality reviews04Handling of statutory audits like Quality, EHS, KSPCB, -CDSCO, weight & scale inspector, Director of Factories & Boilers, Social audits etc and their compliance (Evaluated by No show cause notice and no complaints)05Making sure that critical deviations are investigated and resolved;06Approving all specifications and master production instructions, Test methods, Qualifications07Approving all procedures impacting the quality of intermediates or APIs08Making sure that quality related complaints are investigated and resolved09Adhering to QA budget.10To qualify company for various certifications.11Assuring QMS in all Units.