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时间:2020-03-30
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1、上海*****有限公司文件名称不合格品管理规程第1页文件编号FD2012·03-10修订号A1共4页文件类型标准管理规程执行日期2012-10-12复印数量3分发部门QA、QC、物控部、生产部、技术部1.目的:···································································································22.范围:···················································
2、················································23.责任人:································································································24.依据:···································································································25.内容
3、:···································································································26.附件:···································································································36.1.变更历史···············································
4、·········································36.2.相关记录和文件:·········································································3部门姓名签名日期起草人QA审核人物控部审核人QC审核人生产部审核人技术部审核人QA批准人质量部上海*****有限公司文件名称不合格品管理规程第2页文件编号FD2012·03-10修订号A1共4页文件类型标准管理规程执行日期2012-10-12复印数量3分发部门QA、
5、QC、物控部、生产部、技术部1.目的:对不合格品进行有效管理。2.范围:不符合质量标准的原辅料、包装材料、中间产品、成品。3.责任人:QA、QC、生产部负责人、技术部负责人、物控部负责人。4.依据:不合格物料应有识别标记,并有能够防止未经认可用于生产的隔离制度予以管理。5.内容:5.1.QA判定不合格的物料下发拒绝放行的《产品审核放行单》,张贴不合格证,物控部接到拒绝放行指令后转移物料至不合格品库。5.2.QA填写《不合格品处理报告单》并发放给物控部,物控部据此对不同规格的不合格品作如下处理:5.2.1.不合格原辅料
6、、包装材料处理方法:如果非本公司原因造成的原辅料、包装材料不合格,物控部及时与供货厂商联系退货或换货;如果不能退货或换货,则对不合格原辅料执行《产品销毁管理规程》。5.2.2.不合格品中间产品、成品处理方法:①销毁,执行《产品销毁管理规程》;②返工,执行《产品返工管理规程》;上海*****有限公司文件名称不合格品管理规程第3页文件编号FD2012·03-10修订号A1共4页文件类型标准管理规程执行日期2012-10-12复印数量3分发部门QA、QC、物控部、生产部、技术部③重新加工,执行《产品重新加工管理规程》;5.
7、3.不合格品的存贮:5.3.1.不合格品的存贮应依据《物料储存管理规程》5.1、5.2、5.3项相关规定进行管理,如某类不合格品暂无合适的存贮条件对应的不合格品库,则转入不合格品库后按本规程5.2.2项中的销毁程序执行;5.3.2.不合格品库没有物料存放时,可不需要进行日常温湿度监控。5.3.3.因没有不合格品存放而停止日常温湿度监控工作,需要再次存放不合格品时,不合格品库必须先达到其存贮要求之后,再进行存贮。5.4.不合格品库实行双人双锁管理,库房管理员与QA负责物控部管理的人员各执一把,在有不合格品出入库时同时开
8、锁,不合格品根据本规程5.1项入库,根据5.2项出库,库房管理员填写《不合格品出入库记录》,QA负责物控部管理的人员对此实施监督复核。6.附件:6.1.变更历史:变更原因及目的修订号执行日期6.2.相关记录和文件:产品审核放行单不合格品处理报告单上海*****有限公司文件名称不合格品管理规程第4页文件编号FD2012·03-10修订号A1共4页
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