Quality Assurance Manager - Pharmaceutical Manufacturing

About the role

We are seeking an experienced Quality Assurance Manager to lead QA activities for the production of empty hard gelatin capsules at our Sundar Industrial Estate facility in Lahore. The role focuses on ensuring compliance with GMP, maintaining accurate batch records, and preparing for client inspections.

Key responsibilities

• Oversee creation, review, and approval of Batch Manufacturing Records (BMRs).
• Analyze BMR findings and implement corrective and preventive actions.
• Develop, update, and maintain SOPs specific to capsule production.
• Monitor compliance with industry regulations, company policies, and GMP standards.
• Collaborate with production, QC, and regulatory affairs to resolve quality issues.
• Lead preparation and coordination of factory inspections by pharmaceutical clients.
• Document QA activities, inspection outcomes, and SOP updates for internal and regulatory stakeholders.

Required profile

• Minimum eight years of experience in pharmaceutical quality assurance.
• Strong understanding of quality management systems and regulatory compliance.
• Proven ability to work cross‑functionally and drive continuous improvement.
• Excellent attention to detail and proactive problem‑solving.

Required skills

• Good Manufacturing Practices (GMP) implementation
• SOP development and maintenance
• Batch Manufacturing Records (BMR) management
• Pharmaceutical regulatory compliance
• Factory inspection coordination