Senior Executive QA

1. Area and line clearance for Manufacturing, Packing & Dispensing activity in production area.
2. Inprocess checks in Manufacturing and Packing activity.
3. Inspection of dispensing activity intermediately.
4. Daily verification of weighing balance calibration activity.
5. Daily verification of environmental monitoring of raw material staging area and Manufacturing and Packing area.
6. Verification of each equipment cleanliness and area cleanliness during line clearance
7. Verification and review of online Batch Manufacturing Records. 
8. Sampling of bulk stage and finished goods analysis and control sample. 
9. Verification of production documents.
10. Daily non conformance observation reported and maintained.
11. In process quality checks in Tablet, Liquid, HNH, ANH manufacturing dept. 
12. Line Clearance for Manufacturing, Packing & Dispensing activity.
13. Execution of requirements for food/Dietary supplements regulations for export market (US)-21 CFR Part 111
14. Implementation of effective sanitation program in area.

• QA / QMS / Production experience in Pharma / Food industry
• Understand cGMP requirements as per regulated market requirements
   

B. Pharm or M. Pharm