Quality Control Manager - Pharmaceutical Industry - TJ / 1880779

Recruit AI; Lahore; On-site; PKR 1,800,000 - 3,000,000; Full time

Job summary

Recruit AI in Lahore seeks a Quality Control Manager to lead the QC department in the pharmaceutical industry and ensure product quality and regulatory compliance.

You will develop SOPs, oversee instrument calibration and validation, investigate deviations with root cause analysis, drive CAPA, coordinate audits, and mentor staff while collaborating with Production, R&D, and Procurement.

Qualifications

• Experience leading a QC department.
• Proficient in GMP and ISO 9001 standards.
• Skilled in root cause analysis and CAPA.
• Experience with internal and external audits.

Responsibilities

• Lead the Quality Control department and supervise a team.
• Develop and maintain SOPs for QC testing.
• Ensure GMP/ISO 9001 compliance across QC ops.
• Oversee calibration, validation, and maintenance of lab instruments.
• Coordinate internal and external audits.
• Train and mentor QC staff.
• Report KPIs to senior management.

Skills

Leadership

Quality management

GMP compliance

CAPA investigation

Job description

Our client Recruit AI is looking for a Quality Control Manager - Pharmaceutical Industry in Lahore

The Quality Control Manager will be responsible for developing, implementing, and maintaining testing procedures and standard operating procedures for quality control sampling and testing. This role includes oversight of laboratory instrument calibration and validation, investigation of quality deviations with root cause analysis and corrective actions, coordinating internal and external audits, training and mentoring staff, and collaborating cross-functionally with production, research and development, and procurement teams. The manager consistently monitors supplier and raw material quality, maintains quality records and audit trails, and reports key quality metrics to senior management. Staying current on evolving pharmaceutical regulations and industry best practices is essential to continuously improve the quality management systems and ensure compliance with customer and regulatory requirements.

Responsibilities

• Lead and manage the Quality Control department, supervising a team of 5 personnel and guiding their development and performance.
• Develop, implement, and maintain Standard Operating Procedures (SOPs) for quality control testing of raw materials, in-process samples, and finished goods.
• Ensure compliance with Good Manufacturing Practices (GMP) and ISO 9001 standards across all quality control operations.
• Oversee calibration, validation, and maintenance of laboratory instruments and equipment to guarantee accurate and reliable testing.
• Investigate quality deviations, out-of-specification (OOS) results, and complaints to drive comprehensive root cause analysis and execute corrective and preventive actions (CAPA).
• Prepare, review, and maintain detailed quality documentation, batch records, audit trails, and reports required for internal use as well as regulatory and customer audits.
• Coordinate and lead internal quality audits and participate in external audits conducted by regulatory bodies, customers, and certification bodies to ensure continuous compliance.
• Train and mentor quality control staff on testing protocols, documentation standards, audit readiness, and regulatory requirements to enhance team effectiveness.
• Collaborate closely with Production, Research and Development (R&D), and Procurement teams to address quality-related issues, resolve discrepancies, and support process improvements.
• Monitor supplier and raw material quality, support vendor qualification and ongoing supplier quality assurance to ensure consistency and regulatory compliance.
• Report on quality metrics and key performance indicators (KPIs) including trends and areas for improvement to senior management for strategic decision-making.
• Stay informed of new and evolving pharmaceutical quality regulations, standards, and industry best practices to recommend and implement improvements within the quality system.
• Spearhead continuous improvement initiatives aimed at increasing efficiency, effectiveness, and compliance within the quality control function.