电子厂QE工程师考试试题（供参考），我没时间整答案出来

质量工程师考试试题1.
解说下列名词意义 (18分)
(1)SPC_____________________________
(2)PPM_____________________________
(3)PPK_____________________________
(4)X-R chart_______________________
(5)P chart_________________________
(6)X-Rm chart______________________
(7)PN chart_________________________
(8)σ______________________________
(9)Ca______________________________
(10)Cp_____________________________
(11)CPK__________________________
(12)AQL____________________________
(13)GR &R__________________________
(14)接收者风险______________________

(15)生产者风险_____________________
2.
品管七大手法是哪几种?哪种手法是用来找寻问题的主要矛盾?哪种手法用于制程过程控制?(5分)


3.
管制图有哪两类?简述其如何使用?判定原则(5分)

4.ISO精髓是什么?内部稽核流程?(6分)

4.
什么是FMEA?请举列说明是如何运用.(5分)

6.简述连接器(或线材)产品信赖性测试项目及流程(写出一种即可)(6分)

7.品保工程师如何处理客户抱怨及退货?述论流程?(10分)

8.可靠度定义?其一般材料的失效曲线?(5分)

9.产品尺寸规格10±0.1mm经统计品管得出群体中心值10.05mm,标准差(σ)=0.03mm,请问品保工程师此批量的质量如何?你如何善用质量信息给相关单位或转成公司行动?(10分)


10.量测GR & R的评定原则?(5分)
H与b的同轴度?

若每相邻两点的尺寸为0.635±0.05,那么每个点真实位置(累积误差如何量测?

11.圉中要求如何量测?(10分)




12.(a)图与(b)图的尺寸标示结果有何差异?算出X、Y尺寸范围,并说明差异(附图)(10分)

A图
B图

1. Translation. (5分)

System survey (short form)
(General comments)
Quality policy –goals available but not all metrics are monitored and reviewed NO 8D high defect problems.
Quality planning-No preventive action available ,Management review occurs but no continuous improvement activities carried out ,No benchmarking used.
AQP-No PPAP used. CPK monitored but are questionable. No FMEA used only basic QC flowchart.
C/A & C/I –8D format not used and therefore preventive action and verification does not occur. No deadline requirements for customer complaints.
Do not used a summary list for open/closed CAR.
Gauge-calibration-policy is followed but items can be calibrated the month after the due date .No GR & R used.
Document control-print do not carry the part number that is reverenced by the BOM. No formal deviation process. Good document distribution and recall process.
Purchasing No revision level on the PO. Formal supplier auditing was only instituted this year. Supplier performance is tracked but not forwarded to the supplier and corrective action is not being demanded for poor performance (targets are set too low)
Training No formal training plan for personnel.
Process control –FIFO can't be assured because receiving labels (3 month or 1 color) are used but present on all containers. SPC and CPK are questionable based on the data available .For testers, only a known bad sample is used (not a know good) for verification.
Non-conforming material –Suspect material is generally well labeled but can be found outside of formal MRB areas.
Material control –Trace ability is questionable since receiving labels are removed in production without record being kept. Not using a C=0
Sampling plans for receiving inspection or final inspection.



中间有两张图片，我也懒的处理了，差不多的自己整一个。