JosephERG
Industrial
- Nov 1, 2007
- 20
Hi All!!!
I would just like to ask who formulates the corrective action/s for every non-conforming products that are transferred to QC? As a rule, we all know that the production group has to ensure that all devices transferred to QC must have no "rejects" that is why they perform 100% inspection. If rejects are not effectively filtered, then conducting sampling inspection for QC is dangerous. In our organization, it is the QC engineer (I, being one of them) who is tasked to investigate and formulate corrective actions. I don't think this approach effective. This way, we are not encouraging quality consciousness among our employees. Do you have any ideas on how I can improve the quality consciousness of our production group? Please help.
Thank you.
I would just like to ask who formulates the corrective action/s for every non-conforming products that are transferred to QC? As a rule, we all know that the production group has to ensure that all devices transferred to QC must have no "rejects" that is why they perform 100% inspection. If rejects are not effectively filtered, then conducting sampling inspection for QC is dangerous. In our organization, it is the QC engineer (I, being one of them) who is tasked to investigate and formulate corrective actions. I don't think this approach effective. This way, we are not encouraging quality consciousness among our employees. Do you have any ideas on how I can improve the quality consciousness of our production group? Please help.
Thank you.