Quality Assurance Supervisor

2 weeks ago

Bulacan Philippines Bioessence Group of Companies Full time

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. #J-18808-Ljbffr

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