Pharmaceutical Quality Systems Supervisor

The Assistant Manager QA supports the implementation and maintenance of quality systems to ensure compliance with regulatory standards and internal policies. This role involves supervising QA activities, conducting audits, and driving continuous improvement in pharmaceutical manufacturing processes.

🛠️ Key Responsibilities

• Assist in developing and implementing QA policies, SOPs, and quality systems.
• Lead deviation investigations and market complaint analysis, ensuring timely CAPA execution.
• Conduct internal audits and inspections to ensure GMP compliance.
• Review Batch Manufacturing Records (BMR), Packing Records, APQR, and change controls.
• Monitor production processes and ensure adherence to quality standards.
• Collaborate with cross-functional teams to resolve quality issues and implement corrective actions.
• Train and mentor QA staff on quality procedures and regulatory updates.