Editorial summary

The company is seeking a Quality Assurance Executive with expertise in GMP compliance and pharmaceutical manufacturing to support and enhance its Quality Management System. The role involves ensuring regulatory compliance, maintaining quality standards, and collaborating with manufacturing and cross-functional teams to uphold product quality. The position offers a salary of 4800 and requires a passion for quality assurance and continuous improvement within a dynamic environment.

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Job description

[This job id 22170 first appeared in Job-Q.com on 28 Jul 2026]

Quality Assurance Executive | GMP & Quality Systems

Passionate about Quality Assurance, GMP compliance, and pharmaceutical manufacturing? Join a dynamic team where you'll play a key role in maintaining quality systems, ensuring regulatory compliance, and driving continuous improvement.

🎯 Your Role

As a Quality Assurance Executive, you will support and enhance the company's Quality Management System (QMS), ensure compliance with GMP and regulatory requirements, and work closely with manufacturing and cross-functional teams to uphold product quality and compliance.

📋 Key Responsibilities

• Maintain and continuously improve the Quality Management System (QMS).
• Manage quality documentation, including SOPs, work instructions, specifications, forms, records, and quality reports.
• Ensure compliance with GMP, PIC/S, ICH, ASEAN Guidelines, FDA, and other applicable regulatory standards.
• Coordinate change control activities, including impact assessments, implementation, and timely closure.
• Support deviation investigations, root cause analysis, and CAPA implementation.
• Provide QA support to manufacturing operations and resolve quality-related issues.
• Prepare and review Annual Product Quality Reviews (APQR) and Management Review reports.
• Handle customer complaints, product recalls, returns, and counterfeit investigations.
• Review packaging artwork, specifications, and technical documents for compliance.
• Support equipment qualification, validation activities, machine testing, and trial runs.
• Monitor stability programmes and ensure Good Documentation Practices (GDP) and data integrity.
• Participate in quality improvement projects and support the implementation of electronic Quality Management Systems (eQMS).

Interested candidates, do submit your resume to : jocelynchan@recruitexpress.com.sg OR telegram @jocelynchan

Jocelyn Chan| Consultant | Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R1331820

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