Review and update standard operating procedures (SOPs) to align with changing regulations and best practices. Documentation And Records Management- Maintain and manage documentation related to quality assurance activities, including batch records, investigation reports, change controls, and validation documentation.- Ensure accurate and timely completion of all quality-related documentation. Product Quality Control- Investigate product non-conformances, deviations, and customer complaints to identify root causes and implement appropriate corrective and preventive actions (CAPAs).- Knowledge of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant quality standards.- Making decisions on batch disposition and product recall based on root cause identification.- Reviewing and approving compliance reports following external (customer/regulatory) audits and corporate audits to ensure compliance.- Preparing and implementing quality assurance policies and procedures and ensure that standards and safety regulations are observed.- Timely completion of APQR related activity- Prepared & Review of Validation protocol and report (like Process Validation, Cleaning Validation, Analytical Method Validation,)- Handling of Market Complaint and Related Compliance- Handling of out of specification and suitable investigation- Handling of Deviation and Incident- Prepared BMR, SOP, Protocols etc.- Compliance of Vendor Audit, Regulatory Audit etc.Skills & QualificationEducation:UG: B.Sc / B.PharmPG: M.Sc / M. PharmKnowledge of computer competence, including database managementMinimum Experience Required: 1 - 3 YearCV Required