Pharma QA Officer

Monitor manufacturing activities to ensure compliance with GMP and approved SOPs.

Review BMR/BPR, SOPs, protocols, reports, and other quality documents.

Perform line clearance and in-process quality checks.

Handle and document deviations, CAPA, change controls, and investigations.

Review batch documentation before product release.

Monitor environmental, hygiene, and housekeeping practices in production areas.

Ensure proper implementation of Good Documentation Practices (GDP) and data integrity.

Participate in internal audits, vendor audits, and regulatory inspections.

Coordinate with Production, QC, Warehouse, Engineering, and Regulatory Affairs teams.

Track and close quality-related observations and corrective actions.

Support validation and qualification activities.

Maintain QA records, logs, and quality reports.

Ensure proper handling of complaints, product recalls, and quality incidents when assigned.

Provide GMP and quality-system training to relevant employees.