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An established industry player is seeking a Quality Assurance Specialist to maintain ISO compliance and lead audits. This role involves coordinating with stakeholders, reviewing quality reports, and driving continuous improvements in manufacturing processes. You will be responsible for managing corrective actions and collaborating with production teams to resolve quality issues. Join a dynamic environment where your expertise in quality management and ISO standards will make a significant impact on operational excellence. If you are passionate about quality assurance and thrive in a collaborative setting, this opportunity is perfect for you.
Job Description
Maintain updated and accurate documents and records on ISO 9001, 14001 and 13485 system (includes Quality Manual, Procedures, Work Instructions, Forms, etc.) to ensure system compliance and ready for Management Review.
Plan and conduct internal and external audits to ensure readiness of all sections for third party certification body, management review and customer audits.
Coordinate with internal stakeholders to participate in customer or supplier audits for compliance.
Review audit findings and develop action plans to drive continuous improvements.
Generate and review quality reports on suppliers’ performance and work with suppliers to address non-conforming materials, and drive for continuous improvement.
Issue and follow up on Supplier Corrective Action Request (SCAR) to suppliers, monitor and review SCAR effectiveness for timely closure.
Support the qualification of new suppliers to maintain a healthy pipeline of qualified suppliers to meet Cyrus production requirements.
Maintain and conduct regular review of calibration and preventive maintenance for equipment.
Responsible for quality issues arising from production and customer feedback, and collaborate with the production team to address internal process issues and implement corrective actions to resolve customer complaints with proper documentation.
Responsible for timely closure of Corrective and Preventive Actions (CAPA), non-conformance investigation report and customer complaints and, publish reports on quality performance.
Lead the Material Review Board (MRB) meeting involving members from production, engineering and quality departments to conduct root cause analysis, address quality issues, implement corrective actions and review its effectiveness.
Lead the team of QC inspectors in the inspection of parts for conformity in accordance with relevant drawing requirements.
Job Requirement
Diploma in quality management / Engineering / Manufacturing or related field.
Minimum 3 to 5 years of relevant working experience in handling audits and ISO documentation in manufacturing industries.
Knowledge of quality Management Standards such as ISO 9001, 14001, 13485 and ISO 22301.
HOW TO APPLY:
Interested applicants, kindly send your resume in MS WORD format to ref59(at)trustrecruit.com.sg.
We regret only shortlisted candidates will be notified.
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