Quality Assurance Manager for Supplement Manufacturing

HARMONY PHARMA LAB PTE. LTD.; Singapore; On-site; SGD 33,000 - 67,000; Full time

Benefits offered by this job

5-day work week

No overtime on weekdays

14 days annual leave

Discretionary bonuses

Job summary

Harmony Pharma Lab Pte. Ltd. in Singapore seeks a QA Manager to uphold product quality, regulatory compliance, and manufacturing integrity across multiple dosage forms in the Ubi Area.

You will lead analytical testing, manage documentation, and ensure PIC/S GMP and HALAL standards are met, coordinating with QA, manufacturing, and regulatory teams to drive quality excellence. The role requires precision, accountability, and proactive audits, COAs, batch records, and SOP management to ensure

Qualifications

• Degree in Chemistry or Pharmaceutical Sciences required.
• 3+ years of QA experience in GMP-certified pharma, supplements, or CPM.
• Familiarity with HALAL certification requirements and segregation protocols.
• Knowledge to apply for Certificate of Origin (Computation of Manufacturing Cost Statement).
• Familiar with Product Packaging and regulatory product classification via HSA.

Responsibilities

• Support internal and external audits, including HALAL certification renewals and regulatory inspections.
• Quality Assurance Operations.
• Conduct 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: PIC/S GMP, HALAL, and ASEAN standards.
• Maintain traceability and segregation protocols for HALAL-certified lines.
• Documentation & SOP Management: draft, revise, and implement QC methods and validation protocols.
• Manage controlled documents and align with regulatory changes.
• Support data integrity initiatives and electronic documentation systems.
• Participate in product development and scale-up for QC readiness.
• Monitor trends in product quality and propose preventive actions.

Skills

Strong communications

Analytical techniques

GMP documentation

PIC/S guidelines

Education

Degree in Chemistry/Pharmaceutical Sciences

Job 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:

• Soft Gel
• Hard Capsule
• Liquid/Semi Liquid
• Powder
• Gummy
• Tablet

Key Responsibilities

• 1.Support internal and external audits, including HALAL certification renewals and regulatory inspections.(Note: Key Member to support HSA Audit)
• 2.Quality Assurance Operations
• 3.Conduct routine and non-routine sampling, testing, and release of raw materials, packaging components,in-process samples, and finished products.
• 4.Operate and maintain laboratory instruments and ensure calibration and validation are up to date.
• 5.Review and approve COAs, batch records, and QC reports.
• 6.Regulatory Compliance
• 7.Ensure all QA activities comply with PIC/S GMP, HALAL, and other relevant standards (e.g., BPOM, ASEAN, ISO).
• 8.Maintain traceability and segregation protocols for HALAL-certified production lines.
• 9.Documentation & SOP Management
• 10.Draft, revise, and implement QC-related SOPs, test methods, and validation protocols.
• 11.Manage controlled documents and ensure timely updates in alignment with regulatory changes.
• 12.Support data integrity initiatives and electronic documentation systems.
• 13.Participate in product development and scale-up trials to ensure QC readiness.
• 14.Monitor trends in product quality and propose preventive actions.

Requirements

• 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.

What We Offer

• 1.Basic Salary (SG$3k - SG$6k).
• 2.5 days working days a week (off on Sat and Sun). Working hours 9-6pm or 830 - 530pm.
• 3.No overtime on weekdays.
• 4.14 days annual leave.
• 5.Working location Ubi area near Ubi or Macpherson MRT.
• 6.Discretionary performance-based bonuses.