Executive − Quality Assurance

Piramal Pharma Ltd; Mahad; On-site; INR 350,000 - 700,000; Full time

Job summary

Piramal Pharma Ltd in India seeks an Executive – Quality Assurance to oversee line clearance for Manufacturing, Packing and Dispensing, perform in-process checks, verify documentation, and ensure data integrity.

Responsibilities include calibration verification, environmental monitoring, batch record review, and CAPA implementation to meet export standards and 21 CFR Part 111 requirements.

Qualifications

• B. Pharm or M. Pharm (full time) is essential.
• Experience in QA for pharmaceutical manufacture, packing and dispensing.

Responsibilities

• Area and line clearance for Manufacturing, Packing & Dispensing activity.
• Inprocess checks in Manufacturing and Packing activity.
• Inspection of dispensing activity intermediately.
• Daily verification of weighing balance calibration activity.
• Environmental monitoring of raw material staging and manufacturing areas.
• Review of online Batch Manufacturing Records and production documents.
• Implementation of CAPA and data integrity oversight.

Skills

Quality Assurance

Line clearance

GMP

Documentation

CAPA

EHS

Education

B. Pharm

M. Pharm

Job description

Job Description

Executive − Quality AssuranceExecutive Quality AssuranceJob Description

• 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. Sampling of Bulk and Finished goods
• 14. Review of production records and Finished Goods verification
• 15. On job training to the new people working in the production area.
• 16. Statistical Process Monitoring.
• 17. Online observation of process deviation and effective implementation of CAPA.
• 18. Reporting of daily non conformance.
• 19. Execution of requirements for food/Dietary supplements regulations for export market (US)-21 CFR Part 111
• 20. Ensuring avoidance of breach of data integrity in area.
• 21. Implementation of effective sanitation program in area.
• 22. Imparting required training to shop floor personnel.
• 23. Adherence to the requirements of EHS norms.

Essential Qualification B. Pharm or M. PharmFull time