Key Responsibilities:

- Review and ensure compliance with GMP, GLP, SOPs and regulatory requirements.

- Review Batch Manufacturing Records (BMR), Batch Packing Records (BPR) and other manufacturing documents.

- Perform in-process and shop-floor QA activities.

- Ensure proper documentation and data integrity as per ALCOA+ principles.

- Review and monitor deviations, CAPA, change controls and incidents.

- Assist in internal audits, customer audits and regulatory inspections.

- Verify implementation of approved SOPs and quality procedures.

- Review and approve logbooks, formats, specifications and other QA documents.

- Coordinate with Production, QC, Warehouse and other departments for quality-related activities.

- Monitor cleanliness, hygiene and GMP compliance in manufacturing and other areas.

- Support qualification/validation activities and review related documents.





- Identify quality risks and ensure timely corrective and preventive actions.

- Maintain proper QA records and prepare quality-related reports.

- Ensure compliance with company quality policies and applicable regulatory guidelines.

Required Skills:

- Good knowledge of GMP and pharmaceutical QA practices.

- Valuable documentation and communication skills.

- Knowledge of deviation, CAPA and change control.

- Ability to work independently and coordinate with cross-functional teams.

- Valuable attention to detail and problem-solving ability.

Pay: ₹240,000.00 - ₹300,000.00 per year

Benefits

- Health insurance

- Life insurance

- Provident Fund

Work Location: In person

📌 QA Officer (Ankleshwar)
🏢 Basic Pharma Life Science
📍 Ankleshwar