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用于生产参考的检测项目也需要制定标准么?

小弟,刚开始投入质量体系这行(一个月时间),以前从来没有涉及。
负责体系工作的体系专员(我的老师)最近离职了,新的人员还没有到位。
最近公司又在接受客户的审核,真是焦头兰额
我在的公司是玻璃生产企业,客户在审核的时候提出了这样的问题:
7).In the QC monitor check list(XUG-PG-42-001-A).
A: There is one items"edge width" ,the check frequency is 8time/Shift,but actually record is 4hour/time .A internal memo was shown that the frequency was changed to 4hour/time from 2008.02.25
Why the frequency was changed so big from 1hr/time to 4hr/time ?
Why the record form still kept old version after two month the internal memo issued?
B: There are no specs on the check list. I ask for the spec of edge width A,B,C,D . QC don't know the spec and said the spec was at Hot end engineer side . But when we go to the production side, they can not show the spec and explain it's just a reference data .
No spec, how the QC discover the deviation?
Why is not QC make alarm for deviation ? What's the function of QC ? Just a recorder ?
What's meaning of just as reference control ? No reaction limit?
老师们,对这样的不合格项,我们该怎样着手来改啊?
急!
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负责体系工作的体系专员(我的老师)最近离职了,新的人员还没有到位。6 r8 C9 d/ L# n* F1 z
最近公司又在接受客户的审核,真是焦头兰额
6 k$ ^9 k8 h& W7 O-质量-SPC ,six sigma,TS16949,MSA,FMEA--(20万质量人注册)

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