The QA Officer is responsible for supporting quality assurance activities to ensure that pharmaceutical products are manufactured in compliance with GMP and regulatory standards. The role involves documentation, in-process checks, and coordination with different departments to maintain quality systems.
Key Responsibilities:
- Ensure compliance with GMP (Good Manufacturing Practices) and company quality policies.
- Perform in-process quality checks during manufacturing and packing activities.
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
- Handle deviations, CAPA, change control, and OOS investigations.
- Maintain and update SOPs, formats, and quality documents.
- Monitor line clearance and ensure adherence to procedures.
- Assist in internal audits and regulatory inspections.
- Ensure proper documentation and data integrity practices.
- Coordinate with Production and QC departments for quality-related issues.
- Participate in validation and qualification activities.
- Ensure training compliance for GMP and SOPs.
Requirements:
- Education: B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry or related field)
- Experience: 2–3 years in Quality Assurance (Pharma preferred)
Skills:
- Knowledge of GMP, GLP, and quality systems
- Good documentation and reporting skills
- Attention to detail and analytical thinking
- Basic understanding of pharma manufacturing processes
- Good communication and teamwork skills
Pay: ₹20,000.00 - ₹25,000.00 per month
Work Location: In person
