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Essential Function: 1. To ensure QMS documents are adequately reviewed, approved and stored to be accessible by stake holders in the company. 2. To support QMS manager during customer audits, Certification Bodies audit, and Internal audits. 3. To follow up closely with engineering, purchasing, quality and sales to respond to RoHS/REACH items compliance for customers. 4. Overseeing calibration activities. Responsibilities: 1. Responsible to review, register, update and distribute quality system documents to ensure all documents are complying to QDOS documentation system. 2. To analyse all levels of documents (Quality Manual, SOP, WI, Form & checklist) with internal functional teams for improvement on yearly basis. 3. To monitor all quality records are archived at designated area (Document room,etc) as per retention period stated in Quality Record Archiving SOP. 4. To support QMS manager to perform process, product, system & environment audits at various processes from time to time 5. Responsible to handle external audits such as Customer audit, Certification body audit and Internal audit. 6. To submit RoHS/REACH Compliant documents and meet customer requirements timely. 7. To follow up, monitor and update equipment calibration as per Master list schedule 8. Support purchasing team for suppliers audit. Requirements: 1. Bachelor’s Degree in Quality/Industrial/Material Science Engineering or equivalent. 2. Min. 1-2 years of working experience in QMS within electronics manufacturing environment is highly advantageous. 3. Strong knowledge in ISO 9001, IATF16949 & ISO13485 Quality Management System requirements and able to perform audits independently. 4. Proficiency in Six Sigma, Lean Manufacturing, Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), and Root Cause Analysis (RCA). 5. Words and Excel knowledge at intermediate level will be an added advantage. 6. Strong communication and interpersonal skills, committed & able to meet deadline.