Verify FA, IPQC, MCCL, CTQ, OQA & OBA daily report
Record OQA, OBA and on hold tracker by daily basis
Attend internal and external meeting
Attend new SKU golden sample buyoff
Prepare QSI for new SKU
Assist release package supporting document for new SKU
Assist 8D CAPA supporting document report
Prepare MRF
Update check sheet (IPQC, OQA, CTQ)
Verify manufacturing document (CP, WI, PFMEA)
Assist CP audit
Assist CFT meeting for internal / external issue
Conduct METI data verification
Request rework flow / plan
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