Editorial summary

The company is seeking a QA/QC Assistant in the pharmaceutical sector located in Paya Lebar, for a permanent role on a 5-day workweek with office hours. The position involves preparing, reviewing, revising, and implementing SOPs and other QMS documents in accordance with GMP requirements, ensuring compliance with GMP and company procedures, and performing QC activities including sampling, laboratory testing, and evaluating test results for product disposition. Key requirements include experience with GMP, SOP development, and QA/QC processes within a regulated environment. The role offers a salary range of up to $3,000 monthly.

This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.

Job description

[This job https://singapore.job-q.com/jobs/detail/qa-qc-assistant-up-to-3000-paya-lebar-pharmaceutical-hjy-39416 first appeared in Job-Q.com on 22 Oct 2026]

Location: Paya Lebar
Duration: Permanent
Salary: $2500 - $3000

Working days and hours:
- 5 days, Office Hours

Job Description:
- Prepare, review, revise and implement Standard Operating Procedures (SOPs) and other Quality Management System (QMS) documents in accordance with applicable GMP requirements.
- Ensure compliance with GMP requirements and established company procedures.
- Perform Quality Control (QC) activities, including sampling, arranging laboratory testing according to approved specifications, reviewing analytical/test reports and assessing test results for product disposition.
- Support and/or perform batch/product release activities in accordance with approved specifications and procedures.
- Manage and investigate Out-of-Specification (OOS), deviations, non-conformances and other quality-related issues, including root cause investigation and Implementation of appropriate CAPA.
- Perform sampling and testing activities and coordinate with external testing laboratories where applicable.
- Develop, review and maintain product specifications, test methods, analytical reports, Certificates of Analysis (COA) and related quality documents.
- Plan and coordinate calibration activities in accordance with the Calibration Master Plan.
- Plan, coordinate and perform process and equipment validation activities, including preparation and review of validation protocols and reports.
- Manage stability studies, retention samples, change controls, document control and product technical files.
- Conduct Product Quality Reviews (PQR) and quality risk assessments/management.
- Manage the retention sample room and ensure proper storage, identification and traceability of retention samples.
- Conduct Environmental Monitoring of production areas and review monitoring results to ensure compliance with established requirements.
- Support new product formulation, product development and Research & Development (R&D) activities from a quality and regulatory perspective.
- Conduct GMP training and participate in internal audits, including follow-up and closure of audit findings.
- Conduct and/or participate in supplier, contract manufacturer and external audits.
- Manage customer/product complaints, conduct investigations and propose appropriate CAPA and follow-up actions.
- Support regulatory submissions, product registration and maintenance activities, including liaison with HSA and other relevant regulatory authorities regarding regulatory and quality matters.
- Liaise with internal and external stakeholders to support and streamline the regulatory requirements and export of company products.
- Maintain and continuously improve the company's QMS and ensure effective implementation of quality systems.
- Perform any other duties or activities reasonably assigned by management.|

Job Requirements:
- Min Nitec/Diploma in Science
- Relevant experience would be an added advantage





If interested, please send updated resume via email   

Melissa Zhang Zhiqi (Mezzo)

(CEI.No: R2197564 | Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599)

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