1. Control quality in-process line.
2. Control document for inspection final process.
3. Prepare document for New Model.
4. Control KPI.
5. Customer complain.
6. Warranty claim.
7. Analysis and submit report problem form customer complain, warranty claim and in-process line.
8. Report summary result investigation problem of In-process line by 5 Why or 8D and other report.
1. Supplier assurance.
2. Control follow quality of supplier.
3. Annual and New Model audit supplier.
4. Control inspection received part from supplier.
5. Control WI for Inspection received part from supplier.
6. Issue MRR and MIR to supplier and follow countermeasure report.
7. Evaluation supplier.
8. Request and check PPAP from supplier for New Model and PCR.
9. Control PCR from supplier.
10. Control KPI.
11. Prepare document for New Model.
12. Control quality in-process line.
13. Customer complain.
14. Warranty claim.
15. Analysis and submit report problem form customer complain, warranty claim and in-process line.
16. Report summary result investigation problem of in-process line by 5 Why or 8D and other report.
ประวัติการฝึกอบรม
กรกฎาคม 2561 ถึง กรกฎาคม 2561
STEMMA Co., Ltd.
POTENTIAL FAILURE MODE AND EFFECT ANALYSIS (PFMEA)