• Review of all Batch Production and control Records.• Review of Finish Product & Key starting raw material Analytical documents.• Prepare of Standard Operating Procedures.• Prepare of Annual Product Review.• Review of Deviation System.• Evaluation and Implementation of Change control proposals.• Handling of Customer audits.• Review of Audit points and Implementation of CAPA. • Handling of Market complaints.• Implementation of on-line inspection system and procedures of Quality Assurance.• Supporting the production team in quality issues, ensuring- Compliance with GMP regulation.• Conducting of internal quality audits in all concern departments within the Organization.• Implementation of product release system.• Application of my knowledge in OOS.• Implementation of Changes/Deviations.• Implementation of GMP practices in the facility.• Update & review Bill of Materials (BOM).• Activity of Temperature Mapping Carried out in Ware Houses & Control Sample room.• Training conducting at floor for operators & workers for implementation concept of GMP.• Handling of Returned goods.