Ensure compliance with GMP, GLP, GDP, and company SOPs.
Prepare, review, issue, and control SOPs, BMRs, BPRs, specifications, and other quality documents.
Review batch manufacturing records (BMR) and batch packing records (BPR) before batch release.
Conduct line clearance before the start of manufacturing and packaging activities.
Perform in-process quality checks during production and packing.
Handle deviations, change controls, CAPA, OOS, OOT, and customer complaints.
Review and approve analytical reports, certificates, and quality documentation.
Conduct internal audits and support external regulatory audits.
Monitor environmental conditions, housekeeping, and GMP compliance across production areas.
Ensure calibration and validation activities are completed as per schedule.
Coordinate with Production, QC, Warehouse, and Regulatory Affairs departments.
Maintain document control and ensure proper record retention.
Conduct GMP training for employees and maintain training records.




Support product release activities and ensure compliance with regulatory requirements.

Required Skills
Good knowledge of GMP, GLP, GDP, WHO-GMP, and regulatory guidelines.
Understanding of pharmaceutical quality systems and documentation.
Knowledge of CAPA, Change Control, Deviations, OOS, and OOT investigations.
Strong documentation and analytical skills.
Valuable communication and problem-solving abilities.
Proficiency in MS Office and ERP systems is an added advantage.

Educational Qualification
B.Pharm / M.Pharm
M.Sc. (Chemistry, Microbiology, Biotechnology, or related discipline)

Experience
1–5 years of experience in Quality Assurance in a pharmaceutical manufacturing company.

Intersted Candidates Can share me your resume :- 90545 52040 Thanks & Regards

Anchal Chaube

Advantages

Pay: ₹15,000.00 - ₹30,000.00 per month

Advantages
Cell phone reimbursement
Food provided
Provident Fund

Work Location: In person

📌 Qa Officer Waghodia (India)
🏢 Bhumi Pharmaceuticals
📍 India