Company Description
Our client is a leading precision engineering and solutions provider in Singapore.
Job Description
- 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
Job Requirements
- 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
Compensation
- Working location: Buroh - Working hours: Monday to Friday (08:30 – 17:30) - Annual leave and medical leaves - Medical benefits