Quality Assurance Supervisor

2 days ago

Pulilan Bulacan, Philippines Bioessence Group of Companies Full time ₱1,500,000 - ₱3,000,000 per year

Benefits

  • Competitive compensation package
  • Performance-based incentives
  • Performance-based salary increase
  • Employee discounts and gift certificates
  • HMO for employee and dependents
  • Above standard leave credits (including birthday leave)
  • Employee engagement events and activities
  • Terms and conditions apply

Responsibilities

A. Quality System Management

  • Supervise and monitor implementation of the company's Quality Management System (QMS).
  • Ensure compliance with GMP, ISO 22716, FDA, and internal quality policies.
  • Develop, review, and update QA-related Standard Operating Procedures (SOPs) and work instructions.
  • Conduct internal audits and coordinate external regulatory or certification audits.
  • Manage documentation control, ensuring all quality records are complete, accurate, and properly archived.

B. In-Process & Finished Product Quality

  • Supervise QA inspectors and analysts in conducting incoming, in-process, and finished product inspections.
  • Verify that batch manufacturing records (BMRs) and packaging records are properly completed and reviewed.
  • Coordinate with Production, QC, and R&D departments to resolve product quality issues.

C. GMP & Regulatory Compliance

  • Conduct regular GMP and hygiene inspections in all production areas.
  • Train employees on GMP, Quality Awareness, and Good Documentation Practices (GDP).
  • Ensure plant compliance with FDA, DOH, and other relevant government regulations.
  • Prepare quality reports and regulatory documentation required for audits and certifications

Qualifications:

  • Bachelor's Degree in Chemistry, Pharmacy, Chemical Engineering, or related science field.
  • Licensed Chemist or Pharmacist preferred (as required by FDA regulations).
  • Minimum of 3–5 years of QA experience in a manufacturing setting (preferably cosmetics, pharmaceutical, or FMCG).
  • Strong knowledge of GMP, ISO 22716, FDA regulations, and quality systems.

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