Assisted the QA team in monitoring and maintaining the quality of pharmaceutical products in compliance with GMP (Good Manufacturing Practices) and regulatory guidelines.Conducted routine inspections of manufacturing processes, including reviewing batch records and documentation to ensure accuracy and completeness.Supported the development and implementation of standard operating procedures (SOPs), quality control protocols, and deviation investigations.Performed root cause analysis… Show more Assisted the QA team in monitoring and maintaining the quality of pharmaceutical products in compliance with GMP (Good Manufacturing Practices) and regulatory guidelines.Conducted routine inspections of manufacturing processes, including reviewing batch records and documentation to ensure accuracy and completeness.Supported the development and implementation of standard operating procedures (SOPs), quality control protocols, and deviation investigations.Performed root cause analysis for deviations and non-conformance reports, working closely with cross-functional teams to implement corrective actions.Assisted in internal audits and participated in CAPA (Corrective and Preventive Actions) meetings to ensure continuous process improvement.Collaborated with quality control teams to ensure that all finished products met required specifications and quality standards before release.Gained hands-on experience in regulatory compliance, such as working with FDA and ICH guidelines, and product recalls.Utilized quality management systems (QMS) for tracking and managing quality-related data and ensuring document control. Show less