Quality Assurance Supervisor
1 week ago
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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