Senior Executive-QA

Piramal Pharma Ltd; Mahad; On-site; INR 450,000 - 650,000; Full time

Job summary

Piramal Pharma Ltd in Maharashtra, Mahad is seeking a Senior Executive-QA to support quality assurance in manufacturing, packaging and dispensing. The role emphasizes line clearance, in-process checks, batch record review, CAPA implementation, environmental monitoring and data integrity.

Responsibilities include daily calibration checks, process deviation observation, training of shop floor personnel and ensuring regulatory compliance for export markets.

Qualifications

• B.Pharm or M.Pharm degree required (full time).
• Experience in QA for pharmaceutical manufacturing is preferred.
• Familiarity with regulatory guidelines and data integrity.
• Exposure to 21 CFR Part 111 for export markets is an added advantage.

Responsibilities

• Area and line clearance for Manufacturing, Packing & Dispensing activities.
• In-process checks during manufacturing and packaging.
• Online review of Batch Manufacturing Records and finished goods verification.
• Daily verification of equipment calibration and environmental monitoring.
• Conduct on-job training and ensure adherence to EHS norms.

Skills

Quality Assurance

GMP Compliance

Documentation

CAPA

Education

B.Pharm

M.Pharm

Job description

Job Description

Senior Executive-QAExecutive 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.
• 24. Audit compliance, Qualification and validation activities

Essential Qualification B. Pharm or M. PharmFull time