Industry: Manufacturing / Production
Specialism: Production / Manufacturing - Quality Assurance
Posted on 02 Oct 2026
Our client is a leading precision engineering and solutions provider in Singapore.
- Focusing on the quality system, compliance and prevention of quality issues. Manages QMS documentation, ISO/AS/medical requirements, audits, CAPA and continuous improvement
- Manage and maintain the company’s QMS, procedures and quality documentation
- Ensure compliance with ISO 9001, AS9100, ISO 13485 and customer requirements
- Coordinate internal, customer and certification audits
- Manage CAPA, RCA, 8D and corrective actions
- Monitor quality performance and drive continuous improvement
- Ensure proper document control, records and traceability
- Work closely with Production, Engineering and QC to resolve quality issues
- Work closely with the QC Manager to improve overall Quality Department efficiency and effectiveness
- Support customer and supplier quality requirements
- Drive improvements to reduce rejection, rework, scrap and customer complaints
- Diploma / Degree in Quality, Engineering, Manufacturing or related field
- Minimum 5 years of QA / QMS experience in manufacturing or precision engineering
- Good knowledge of ISO 9001
- Knowledge of AS9100 and ISO13485 is an advantage
- Experience in medical, semiconductor or aerospace industries preferred
- Experience in audits, CAPA, RCA and 8D
- Good leadership, communication and problem-solving skills
- Working location: Buroh
- Working hours: Monday to Friday (08:30 – 17:30)
- Annual leave and medical leaves
- Medical benefits