QC Manager

Drlogy; India; On-site; INR 600,000 - 1,200,000; Full time

Job summary

Drlogy is seeking an experienced QC Manager to lead the quality control operations within pharmaceutical manufacturing. Responsibilities include ensuring compliance with GMP and GLP standards, supervising laboratory activities, and coordinating with QA and production teams.

The ideal candidate will possess skills in laboratory management and quality assurance systems, supporting audits and regulatory inspections while maintaining documentation systems.

Qualifications

• Experience managing quality control operations within pharmaceutical manufacturing.
• Skilled in ensuring product quality and regulatory compliance.
• Adept at laboratory management and analytical testing.

Responsibilities

• Manage daily quality control laboratory operations efficiently.
• Ensure compliance with GMP, GLP, and quality standards.
• Supervise analytical testing of raw materials and finished products.
• Review analytical reports and laboratory documentation accurately.
• Investigate out-of-specification and quality-related issues.

Skills

Laboratory management

Analytical compliance

Team supervision

Quality assurance systems

Job description

Experienced QC Manager responsible for managing quality control operations, laboratory activities, and analytical testing within pharmaceutical manufacturing environments. Skilled in laboratory management, analytical compliance, team supervision, and quality assurance systems. Adept at ensuring product quality, regulatory compliance, and efficient laboratory operations.

Responsibilities

• Manage daily quality control laboratory operations efficiently.
• Ensure compliance with GMP, GLP, and quality standards.
• Supervise analytical testing of raw materials and finished products.
• Review analytical reports and laboratory documentation accurately.
• Coordinate calibration and maintenance of laboratory equipment.
• Investigate out-of-specification and quality-related issues.
• Monitor laboratory performance and operational efficiency metrics.
• Coordinate with QA and production departments for quality compliance.
• Ensure proper handling and storage of laboratory chemicals and samples.
• Support audits and regulatory inspection readiness activities.
• Train QC staff on laboratory procedures and compliance standards.
• Maintain laboratory records and quality documentation systems.
• Implement process improvement and quality enhancement initiatives.
• Ensure timely completion of testing and reporting activities.
• Maintain safety and operational standards within laboratory areas.