Assistant Manager Quality Assurance
Indus Pharmaceutical
Total des années d'expérience :5 years, 2 Mois
• Enforcement of quality production. (GMP & GDP)
• Identifying deviations and reporting to the manager quality assurance.
• Writing and reviewing the SOPs.
• Release of drug product for market through ERP
• Cross check of all inventory in warehouse and audit an area.
• Monitor dispensing of Raw material and packaging material.
• Auditing Batch Documents
• To ensure finish product quality with quantity.
• Lead PQR team to implement CAPA on over all PQR of year.
• Documentation.
• To approve and issue material on ERP system
• Auditing batch documents.
• Working with CAPA committee.
• Enforcement of quality production.
• Identifying deviations and reporting to the manager quality assurance.
• Writing and reviewing the SOPs.
• Dispensing Of Materials.
• To work on vendor complaint, costumer complaint
• To control and complete change control actions
• To assist validation officer for batch validation as well as facilities and equipments
• To work on Root Cause Analysis (RCA) and problem solving.
• Arrange and deliver cGMP Training to staff
In process checks of non sterile area (Tablet, Capsule, Liquid, Dry Powder)
•Check the dispensing material, packaging material, and monitor bin card
•Audit BMR
•Plan, conduct and monitor testing and inspection of materials and products.
•To ensure finished product quality with quantity.
•Implementation of CAPA
•GMP Compliance
•Monitor risk management
•Document management systems
•Preparing and reviewing the SOP.
•Verify rejection and return material.
Pharm-D with cGPA 3.12, December