Quality Control Supervisor - Chemist

About the role

This role involves supervising QC personnel and ensuring smooth quality assurance and quality control operations in a pharmaceutical or manufacturing environment. You will oversee daily activities, review critical documentation, conduct inspections and audits, and manage quality-related processes to ensure GMP compliance and product quality standards.

Key responsibilities

• Supervise the daily activities of QC personnel and ensure smooth QC operations
• Review In-Process Monitoring Records for completeness, accuracy, and timely submission
• Prepare weekly work schedules and adjust staff assignments as needed
• Review and verify the correct revision of Master Batch Records/Packaging Batch Records (MBR/PBR) before release to Production
• Conduct inspections of production areas and warehouses to ensure GMP compliance
• Review and approve Packaging Material Inspection Reports (PMIRs) and corresponding approved stickers
• Conduct internal audits of production areas and warehouses with the GMP Team
• Conduct audits of new raw material and packaging material suppliers
• Analyze validation, product quality review, and product stability data and prepare corresponding reports
• Handle investigations related to product complaints and process deviations

About you

• Bachelor's Degree in Chemistry, Pharmacy, or a related field
• Licensed Chemist is preferred/required, depending on regulatory requirements of the role
• At least 3–5 years of experience in Quality Control, preferably in a pharmaceutical, manufacturing, or laboratory environment
• Supervisory or team-leadership experience is highly preferred
• Strong knowledge of GMP, GLP, QMS, SOPs, documentation control, and quality assurance practices
• Experience in batch record review, audits, validation, investigations, and product release is an advantage
• Knowledge of pharmaceutical manufacturing processes and regulatory requirements
• Strong analytical, problem-solving, organizational, and leadership skills
• Detail-oriented with excellent documentation and communication skills
• Willing to work on-site and handle shifting schedules when required