Responsible for leading and managing QMS improvement initiative across all departments and functions to ensure quality initiatives and quality plans are executed and maintained in full compliance with IATF requirements. This includes addressing issues from quality management oversight and helping the site management team to execute effectively the quality enhancement activities.
Drive and apply risk management principles based on the analysis of context of organization, formulate goals and objectives to address risk and opportunities as part of organization strategy and performance indicators.
Set Quality Objectives, review and report its achievement status periodically and propose necessary actions.
Cost Budget Control of Quality Department
Review and approve the Management of Change (MOC) and Non Regular Work (NRW).
Lead, manage and supervise QA and QC laboratory personnel
Review and approve IATF Core Tools Reporting: SPC, FMEA, MSA, and GR&R
Review PPAP documents according to customer level of quality requirements
Drive continuous improvement and support R&D department on new product development.
Provide direction and implement Process / Final Inspection, approve Product Grading, Rework and review of non-conforming products
Non conformity correction, storage, identification, logistics (shipment) work of final product.
Manage, review and control of QC laboratory, equipment calibration, maintenance and spare parts.
Degree in engineering or chemistry (BS Chemical Engineering / Chemistry) or equivalent.
10 years plus working experience in quality such as lab testing or in Quality Assurance department.
Strong knowledge and understanding of ISO 9001, IATF 16949 or similar quality systems and experience in facing quality audits.
Demonstrated leadership skills including teamwork, communication, prioritization and change management
We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh| Registration No: R1109239