Quality Control Supervisor - Chemist

EAST ASIA LABORATORIES INC.; Marikina; On-site; PHP 446,000 - 781,000; Full time

Job summary

EAST ASIA LABORATORIES INC. in the Philippines seeks a skilled QC Supervisor to oversee QC activities, ensure GMP compliance, and maintain high product quality. You will review critical records, lead audits, and manage investigations related to deviations.

The role requires a Bachelor's in Chemistry or Pharmacy, 3–5 years in QC, and supervisory experience. On-site work at facilities in San Mateo, Rizal and Marikina is expected, with shifting schedules as needed.

Qualifications

• Bachelor's degree in Chemistry, Pharmacy, or related field.
• Licensed Chemist preferred/required depending on regulatory requirements.
• 3–5 years of experience in Quality Control in pharmaceutical, manufacturing, or laboratory environments.
• Supervisory or team-leadership experience preferred.
• Strong knowledge of GMP, GLP, QMS, SOPs, documentation control, and quality assurance practices.

Responsibilities

• Supervise daily 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 before release to Production
• Conduct inspections of production areas and warehouses to ensure GMP compliance
• Review and approve PMIRs and corresponding approved stickers
• Conduct internal GMP audits of production areas and warehouses
• 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

Skills

GMP knowledge

Quality Assurance

Leadership

Documentation

Audits

Education

Bachelor's degree in Chemistry/Pharmacy/related field

Tools

Quality Management System (QMS)

Job description

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
• Willing to work in San Mateo, Rizal and Marikina