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Quality Systems & Compliance

• Support implementation and maintenance of the Pharmaceutical Quality Management System (PQMS).
• Ensure compliance with GMP, regulatory, and internal quality requirements.
• Participate in internal audits, inspections, and quality reviews.

Documentation & Record Control

• Review, approve, and manage controlled documents including SOPs, batch records, and quality manuals.
• Ensure accurate and timely documentation in line with regulatory standards.

Deviation, CAPA & Change Control

• Support investigation of deviations, non-conformances, and customer complaints.
• Assist in implementing Corrective and Preventive Actions (CAPA).
• Participate in change control processes to maintain product quality and compliance.

Batch Release & Quality Oversight

• Review batch manufacturing and packaging records prior to release.
• Ensure only compliant products are released to the market.

Training & Continuous Improvement

• Support GMP and quality-related training for staff.
• Participate in continuous improvement initiatives within the quality function.