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ISO/TS16949 APQP Zero Defect 달성을 위한 개발기법의 적용사례에 관한 연구

원문정보

The ISO/TS16949 the research regarding the application instance of the development technique for a APQP zero defect attainment

문찬오

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초록

영어

The ISO/TS16949 APQP goal of defect prevention and decrease of spread waste, is the customer satisfaction which leads a continuous improvement and profit creation. The quality expense where the most is caused by but with increase of production initial quality problem occurrence is increasing to is actuality. Like this confirmation amendment. with the problem which is forecast in the place development at the initial stage which it does completeness it does not confront not to be able, production phase to be imminent, the problem accumulates and it talks the development shedding of which occurs. In opposition, prediction confrontation. is forecast in development early stage to and it is a structure which does not occur a problem to production early stage. Like this development is a possibility of accomplishing competitive company from production phase. Which attains an goal of, chance cause it leads a APQP activity (common cause) with special cause prevention & detection the connection characteristic of the focus technique against a interaction is important. And the customer requirement satisfaction and must convert a APQP goal of attainment at the key characteristics action step. (1) The Prevention - with Design FMEA application prevention of the present design management/detection, (2) the Detection (prevention/detection) - with Process FMEA application prevention of the present process control/detection, (3) Special Cause - statistical process control (SPC) 4M cause spread removal, (4) Common Cause - statistical process control (SPC) the nothing zero defect which leads the continuous improvement back of spread with application it will be able to attain with application.

목차

Ⅰ. 서 론
 Ⅱ. 이론적 배경
  1. ISO/TS16949:2002 탄생 배경
  2. 사전제품품질계획(APQP) 전제조건
 Ⅲ. APQP 개발단계의 적용사례
  1. 프로그램계획 및 정의(1단계)
  2. 제품설계 및 개발 (2단계)
  3. 공정설계 및 개발(3단계)
  4. 제품 및 공정유효성확인(4단계)
  5. 피드백, 평가 및 시정조치(5단계)
 Ⅳ. 결 론
 참고문헌
 Abstract

저자정보

  • 문찬오 Moon, Chan-oh. 명지대학교 산업공학과

참고문헌

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