Quality Assurance Manager for Supplement Manufacturing
- Compensation
- SGD 2K–SGD 4.5K / mo
- Location
- Singapore
- Work setup
- Not specified
- Seniority
- Not specified
- Employment
- Not specified
- Experience
- 3+ years
- Category
- Qa
- Posted
Skills
Must have
- 1. Degree in Chemistry, Pharmaceutical Sciences, or related field.
- 2. 3+ years of QA experience in GMP-certified pharmaceutical, supplement, or Chinese proprietary medicine (CPM)
- 3. Familiarity with HALAL certification requirements and segregation protocols.
- 4. Knowledge to apply for Certificate of Origin (Computation of Manufacturing Cost Statement)
- 5. Familiar with Product Packaging and get regulatory product classification done through HSA.
- 6. Proficient in analytical techniques and GMP documentation practices.
- 7. Strong understanding of PIC/S guidelines and ASEAN regulatory frameworks.
- 8. Strong communications skills.
Full description
Job Title
QA Manager
Occupation
Quality Assurance Manager
Job Description & Requirements
Location: Singapore, Ubi Area
Facility Type: PIC/S HSA GMP-Certified Pharmaceutical & Supplement Manufacturing Plant
Certifications: HALAL, HSA PIC/S GMP, INTERTEK GMP
About the Role
As a QA Manager, you will play a critical role in ensuring product quality, regulatory compliance, and operational integrity across all stages of manufacturing. You’ll lead analytical testing, manage documentation, and uphold standards aligned with PIC/S GMP and HALAL requirements. This position demands precision, accountability, and cross-departmental coordination to support multi-dosage production:
a) Soft Gel
b) Hard Capsule
c) Liquid/Semi Liquid
d) Powder
e) Gummy
f) Tablet
Key Responsibilities
- Support internal and external audits, including HALAL certification renewals and regulatory inspections.(Note: Key Member to support HSA Audit)
- Quality Assurance Operations
- Conduct routine and non-routine sampling, testing, and release of raw materials, packaging components,in-process samples, and finished products.
- Operate and maintain laboratory instruments and ensure calibration and validation are up to date.
- Review and approve COAs, batch records, and QC reports.
- Regulatory Compliance
- Ensure all QA activities comply with PIC/S GMP, HALAL, and other relevant standards (e.g., BPOM, ASEAN, ISO).
- Maintain traceability and segregation protocols for HALAL-certified production lines.
- Documentation & SOP Management
- Draft, revise, and implement QC-related SOPs, test methods, and validation protocols.
- Manage controlled documents and ensure timely updates in alignment with regulatory changes.
- Support data integrity initiatives and electronic documentation systems.
- Participate in product development and scale-up trials to ensure QC readiness.
- Monitor trends in product quality and propose preventive actions.
Requirements
- Degree in Chemistry, Pharmaceutical Sciences, or related field.
- 3+ years of QA experience in GMP-certified pharmaceutical, supplement, or Chinese proprietary medicine (CPM)