Quality Assurance Manager – Pharmaceutical Manufacturing

About the role

Our client is seeking an experienced Quality Assurance Manager to lead QA activities within a pharmaceutical manufacturing environment in Lahore. The role focuses on ensuring batch records, SOPs and inspections meet regulatory standards while supporting cross‑functional teams.

Key responsibilities

• Oversee preparation, review and approval of Batch Manufacturing Records (BMRs) to ensure compliance with regulatory requirements.
• Implement and monitor corrective and preventive actions derived from BMR findings.
• Develop, write and update Standard Operating Procedures (SOPs) for the production of empty hard gelatin capsules.
• Monitor ongoing compliance with regulatory frameworks, company policies and quality standards.
• Collaborate with production, quality control and regulatory affairs to resolve quality and compliance issues.
• Lead coordination and preparation for factory inspections conducted by customer inspection teams.
• Address non‑conformities identified during inspections and drive effective corrective measures.
• Maintain comprehensive documentation of QA activities, audit findings and quality metrics.

Required profile

• Bachelor’s degree in Pharmacy.
• Minimum six years of experience in a pharmaceutical quality department.
• Strong understanding of industry regulations, quality systems and manufacturing practices.
• Excellent communication and collaborative skills.
• Ability to work under pressure while maintaining high‑quality standards.

Required skills

• Batch Manufacturing Records (BMR) management.
• Standard Operating Procedures (SOP) development.
• Regulatory compliance in pharmaceutical manufacturing.
• Quality systems implementation and audit support.