SlideShare ist ein Scribd-Unternehmen logo
1 von 57
APQP PPAP
PPAP 引言 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
PPAP 引言 ,[object Object],[object Object],[object Object],[object Object]
PPAP 引言 ,[object Object],[object Object],[object Object]
PPAP 引言 ,[object Object],[object Object]
PPAP 引言 ,[object Object],[object Object],[object Object],[object Object]
PPAP 引言 ,[object Object],[object Object]
APQP A Perspective on 8-D and PFMEA and Control Plan During APQP and Afterwards
What is APQP? ,[object Object],[object Object],[object Object]
Benefits of APQP ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Customer and Supplier Involvement ,[object Object],[object Object],[object Object]
Determine Customer Requirements ,[object Object],[object Object],[object Object],[object Object],[object Object]
Training ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
APQP Five Phase Process Planning Product Design and Development Process Design and Development Product and Process Validation Production Feedback Assessment and Corrective Action Pilot Launch Concept Initiation/Approval Program Approval Prototype Planning
Links Between the Tools Contract Review Program Plan DFMEA Team Feasibility Commitment Produce Process Flow Diagrams Conduct Process FMEA Develop Control Plan Work Instruction Development Product and Process Validation Ensure Continuous Improvement Phase I Phase II Phase II Phase III Phase III Phase III Phase III Phase IV Phase V Determine Customer Expectations and Plan for Quality Identify Key Characteristics  Determine Risk and Feasibility Associate Characteristics with Process Steps and Identify Key Characteristics Expose Sources of Variation and Finalize Key Characteristics Determine Methods to Improve Process and Control Variation Implement Control Plan and Standardize the Process Ensure Customer Expectations are Met Exercise Management Oversight
The Target and The Goal
Link Between the Documents
Process Flow Diagrams ,[object Object],[object Object],[object Object],[object Object]
Process Flow Diagram Example
APQP Links to PFMEA
Process FMEA ,[object Object],[object Object]
How a PFMEA Works ,[object Object],[object Object],[object Object]
PFMEAs/Control Plans and 8-Ds During APQP ,[object Object],[object Object],[object Object],[object Object]
APQP Links to Control Plan
Control Plans ,[object Object],[object Object],[object Object],[object Object]
Types of Control Plans ,[object Object],[object Object],[object Object]
Prototype Build Control Plan ,[object Object],[object Object],[object Object]
Pre-launch Control Plan ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Production Control Plan ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Control Plan Use ,[object Object],[object Object],[object Object]
Multiple Molds, Tools, Dies and Patterns ,[object Object],[object Object]
Part Submission Status ,[object Object],[object Object],[object Object]
Automotive Documentation Development Develop  Process Flow Listing Check for  Customer Requirements Enter Every  “Major”  Process from  Flow Listing  into  FMEA Form  Give careful consideration to what you consider a  “Major”  process Develop  FMEA  Element for  Every  Process Use the appropriate  RPN  numbers and considerations of other appropriate information / data to determine  Critical  characteristics Develop the  Control Plan  with  Critical  Characteristics Develop  control mechanisms  appropriate for  Critical  characteristics. Give careful consideration to defining Control Plan stages Prototype Pre-launch Production
 
[object Object],[object Object]
PPAP Purpose ,[object Object],[object Object]
PPAP Scope ,[object Object],[object Object],[object Object]
Base Documentation ,[object Object],[object Object],[object Object],[object Object],[object Object]
General ,[object Object],[object Object],[object Object],[object Object],[object Object]
General ,[object Object],[object Object]
Elements of a PPAP ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Parts Submission Warrant ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Part Weight ,[object Object],[object Object],[object Object],[object Object],[object Object]
Master Sample ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Preliminary Process Capability Studies ,[object Object],[object Object],[object Object],[object Object],[object Object]
Production Trial Run ,[object Object],[object Object],[object Object],[object Object]
Production Trial Run Product Used For ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Measurement System Analysis (MSA) ,[object Object],[object Object],[object Object]
Packaging Evaluation ,[object Object],[object Object],[object Object],[object Object]
Floor Plan Layout ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Review and Sign-Off ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Quality Problems yes no no yes no yes no yes
Cause unknown ,[object Object],Note: When a customer problem occurs, follow customer prescribed methodology
When to use 8-D ,[object Object],[object Object],[object Object],Note: We use voting techniques, X to Y variable testing, and IS/IS Not to determine the root cause.  However, you still may not know what the root cause is?
Update the PFMEA & Control Plans After the 8-D is completed, the PMEA and the control plan should be revised and updated as applicable Process  Flow PFMEA Control  Plan Work  Instruction Scrap, Rework Data Warranty & Assembly Plant Data
[object Object]

Weitere ähnliche Inhalte

Was ist angesagt?

Was ist angesagt? (20)

Advanced Product Quality Planning presentation
Advanced Product Quality Planning presentationAdvanced Product Quality Planning presentation
Advanced Product Quality Planning presentation
 
Fmea handout
Fmea handoutFmea handout
Fmea handout
 
Ppap training presentation
Ppap   training presentationPpap   training presentation
Ppap training presentation
 
Advanced Pfmea
Advanced PfmeaAdvanced Pfmea
Advanced Pfmea
 
Apqp-en
Apqp-enApqp-en
Apqp-en
 
PROCESS FAILURE MODE EFFECTS ANALYSIS (PFMEA) PPT
PROCESS FAILURE MODE EFFECTS ANALYSIS (PFMEA) PPTPROCESS FAILURE MODE EFFECTS ANALYSIS (PFMEA) PPT
PROCESS FAILURE MODE EFFECTS ANALYSIS (PFMEA) PPT
 
Fmea
FmeaFmea
Fmea
 
Apqp process flow
Apqp process flowApqp process flow
Apqp process flow
 
Process fmea
Process fmea Process fmea
Process fmea
 
Training ppt for control plan
Training ppt for control plan   Training ppt for control plan
Training ppt for control plan
 
Ppap training ppt
Ppap training   ppt Ppap training   ppt
Ppap training ppt
 
APQP
APQPAPQP
APQP
 
Cost of-poor-quality - juran institute
Cost of-poor-quality - juran instituteCost of-poor-quality - juran institute
Cost of-poor-quality - juran institute
 
APQP
APQP APQP
APQP
 
PPT ON DESIGN FAILURE MODE AND EFFECT ANALYSIS (DFMEA)
PPT ON DESIGN FAILURE MODE AND EFFECT ANALYSIS (DFMEA)PPT ON DESIGN FAILURE MODE AND EFFECT ANALYSIS (DFMEA)
PPT ON DESIGN FAILURE MODE AND EFFECT ANALYSIS (DFMEA)
 
Failure Mode & Effect Analysis
Failure Mode & Effect AnalysisFailure Mode & Effect Analysis
Failure Mode & Effect Analysis
 
The Basics 7 QC Tools - ADDVALUE - Nilesh Arora
The Basics 7 QC Tools - ADDVALUE - Nilesh AroraThe Basics 7 QC Tools - ADDVALUE - Nilesh Arora
The Basics 7 QC Tools - ADDVALUE - Nilesh Arora
 
Ppap training-presentation
Ppap training-presentationPpap training-presentation
Ppap training-presentation
 
Ppap la
Ppap laPpap la
Ppap la
 
Failure Modes and Effect Analysis (FMEA)
Failure Modes and Effect Analysis (FMEA)Failure Modes and Effect Analysis (FMEA)
Failure Modes and Effect Analysis (FMEA)
 

Andere mochten auch

先期產品品質規劃 華宇
先期產品品質規劃  華宇先期產品品質規劃  華宇
先期產品品質規劃 華宇營松 林
 
Zhiii skincare fe&r12(for media) 20110906
Zhiii skincare fe&r12(for media) 20110906Zhiii skincare fe&r12(for media) 20110906
Zhiii skincare fe&r12(for media) 20110906營松 林
 
02training material for msa
02training material for msa02training material for msa
02training material for msa營松 林
 
2.ie培訓教材
2.ie培訓教材2.ie培訓教材
2.ie培訓教材營松 林
 
02 spc訓練教材
02 spc訓練教材02 spc訓練教材
02 spc訓練教材營松 林
 
02 fmea training
02 fmea training02 fmea training
02 fmea training營松 林
 
03 fmea表格使用說明
03 fmea表格使用說明03 fmea表格使用說明
03 fmea表格使用說明營松 林
 
全面品質管理 東吳王超弘
全面品質管理  東吳王超弘全面品質管理  東吳王超弘
全面品質管理 東吳王超弘營松 林
 
Manufacturing excellence
Manufacturing excellenceManufacturing excellence
Manufacturing excellence營松 林
 

Andere mochten auch (13)

Get Relief for Your PPAP Grief
Get Relief for Your PPAP GriefGet Relief for Your PPAP Grief
Get Relief for Your PPAP Grief
 
O&E
O&EO&E
O&E
 
5 s book
5 s book5 s book
5 s book
 
先期產品品質規劃 華宇
先期產品品質規劃  華宇先期產品品質規劃  華宇
先期產品品質規劃 華宇
 
Zhiii skincare fe&r12(for media) 20110906
Zhiii skincare fe&r12(for media) 20110906Zhiii skincare fe&r12(for media) 20110906
Zhiii skincare fe&r12(for media) 20110906
 
02training material for msa
02training material for msa02training material for msa
02training material for msa
 
2.ie培訓教材
2.ie培訓教材2.ie培訓教材
2.ie培訓教材
 
02 spc訓練教材
02 spc訓練教材02 spc訓練教材
02 spc訓練教材
 
02 fmea training
02 fmea training02 fmea training
02 fmea training
 
03 fmea表格使用說明
03 fmea表格使用說明03 fmea表格使用說明
03 fmea表格使用說明
 
01 fmea
01 fmea01 fmea
01 fmea
 
全面品質管理 東吳王超弘
全面品質管理  東吳王超弘全面品質管理  東吳王超弘
全面品質管理 東吳王超弘
 
Manufacturing excellence
Manufacturing excellenceManufacturing excellence
Manufacturing excellence
 

Ähnlich wie 04 ppap training material

Core tools apqp, ppap, fmea, spc and msa
Core tools   apqp, ppap, fmea, spc and msa Core tools   apqp, ppap, fmea, spc and msa
Core tools apqp, ppap, fmea, spc and msa Mouhcine Nahal
 
Guidelines to Audit Validation Packages_RGA
Guidelines to Audit Validation Packages_RGAGuidelines to Audit Validation Packages_RGA
Guidelines to Audit Validation Packages_RGARosnelma García
 
Pharmaceutical Qualification & Validation
Pharmaceutical Qualification & ValidationPharmaceutical Qualification & Validation
Pharmaceutical Qualification & ValidationPharmaceutical
 
1MP from Comecer
1MP from Comecer1MP from Comecer
1MP from ComecerComecer
 
Process Validation.pptx
Process Validation.pptxProcess Validation.pptx
Process Validation.pptxRameshAmuluru1
 
Facility & Equipment Quality System Outline
Facility & Equipment Quality System OutlineFacility & Equipment Quality System Outline
Facility & Equipment Quality System OutlineJoseph Busfield
 
Validation Program Design
Validation Program DesignValidation Program Design
Validation Program Designbwbslide
 
Muthaiah profile
Muthaiah profileMuthaiah profile
Muthaiah profileMuthaiah C
 
ADVANCED PRODUCT QUALITY
ADVANCED PRODUCT QUALITYADVANCED PRODUCT QUALITY
ADVANCED PRODUCT QUALITYanish malan
 
GP_Training_APQP-PPAP_RevAF.pptx
GP_Training_APQP-PPAP_RevAF.pptxGP_Training_APQP-PPAP_RevAF.pptx
GP_Training_APQP-PPAP_RevAF.pptxNonameNoname50
 
FMEA.pdf
FMEA.pdfFMEA.pdf
FMEA.pdfinfoqtc
 
Ppap training-presentation-150311063239-conversion-gate01
Ppap training-presentation-150311063239-conversion-gate01Ppap training-presentation-150311063239-conversion-gate01
Ppap training-presentation-150311063239-conversion-gate01BhimKunwar2
 

Ähnlich wie 04 ppap training material (20)

APQP-PPAP[1].ppt for engineering products
APQP-PPAP[1].ppt for engineering productsAPQP-PPAP[1].ppt for engineering products
APQP-PPAP[1].ppt for engineering products
 
PPAP.ppt
PPAP.pptPPAP.ppt
PPAP.ppt
 
Core tools apqp, ppap, fmea, spc and msa
Core tools   apqp, ppap, fmea, spc and msa Core tools   apqp, ppap, fmea, spc and msa
Core tools apqp, ppap, fmea, spc and msa
 
Process validation
Process validationProcess validation
Process validation
 
PPAP.pdf
PPAP.pdfPPAP.pdf
PPAP.pdf
 
Guidelines to Audit Validation Packages_RGA
Guidelines to Audit Validation Packages_RGAGuidelines to Audit Validation Packages_RGA
Guidelines to Audit Validation Packages_RGA
 
Ppap la
Ppap laPpap la
Ppap la
 
Pharmaceutical Qualification & Validation
Pharmaceutical Qualification & ValidationPharmaceutical Qualification & Validation
Pharmaceutical Qualification & Validation
 
1MP from Comecer
1MP from Comecer1MP from Comecer
1MP from Comecer
 
Process Validation.pptx
Process Validation.pptxProcess Validation.pptx
Process Validation.pptx
 
pourush C.V
pourush C.Vpourush C.V
pourush C.V
 
APQP FLOW CHART.pptx
APQP FLOW CHART.pptxAPQP FLOW CHART.pptx
APQP FLOW CHART.pptx
 
Facility & Equipment Quality System Outline
Facility & Equipment Quality System OutlineFacility & Equipment Quality System Outline
Facility & Equipment Quality System Outline
 
Validation Program Design
Validation Program DesignValidation Program Design
Validation Program Design
 
Ppaptr
PpaptrPpaptr
Ppaptr
 
Muthaiah profile
Muthaiah profileMuthaiah profile
Muthaiah profile
 
ADVANCED PRODUCT QUALITY
ADVANCED PRODUCT QUALITYADVANCED PRODUCT QUALITY
ADVANCED PRODUCT QUALITY
 
GP_Training_APQP-PPAP_RevAF.pptx
GP_Training_APQP-PPAP_RevAF.pptxGP_Training_APQP-PPAP_RevAF.pptx
GP_Training_APQP-PPAP_RevAF.pptx
 
FMEA.pdf
FMEA.pdfFMEA.pdf
FMEA.pdf
 
Ppap training-presentation-150311063239-conversion-gate01
Ppap training-presentation-150311063239-conversion-gate01Ppap training-presentation-150311063239-conversion-gate01
Ppap training-presentation-150311063239-conversion-gate01
 

04 ppap training material

  • 2.
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8. APQP A Perspective on 8-D and PFMEA and Control Plan During APQP and Afterwards
  • 9.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14. APQP Five Phase Process Planning Product Design and Development Process Design and Development Product and Process Validation Production Feedback Assessment and Corrective Action Pilot Launch Concept Initiation/Approval Program Approval Prototype Planning
  • 15. Links Between the Tools Contract Review Program Plan DFMEA Team Feasibility Commitment Produce Process Flow Diagrams Conduct Process FMEA Develop Control Plan Work Instruction Development Product and Process Validation Ensure Continuous Improvement Phase I Phase II Phase II Phase III Phase III Phase III Phase III Phase IV Phase V Determine Customer Expectations and Plan for Quality Identify Key Characteristics Determine Risk and Feasibility Associate Characteristics with Process Steps and Identify Key Characteristics Expose Sources of Variation and Finalize Key Characteristics Determine Methods to Improve Process and Control Variation Implement Control Plan and Standardize the Process Ensure Customer Expectations are Met Exercise Management Oversight
  • 16. The Target and The Goal
  • 17. Link Between the Documents
  • 18.
  • 20. APQP Links to PFMEA
  • 21.
  • 22.
  • 23.
  • 24. APQP Links to Control Plan
  • 25.
  • 26.
  • 27.
  • 28.
  • 29.
  • 30.
  • 31.
  • 32.
  • 33. Automotive Documentation Development Develop Process Flow Listing Check for Customer Requirements Enter Every “Major” Process from Flow Listing into FMEA Form Give careful consideration to what you consider a “Major” process Develop FMEA Element for Every Process Use the appropriate RPN numbers and considerations of other appropriate information / data to determine Critical characteristics Develop the Control Plan with Critical Characteristics Develop control mechanisms appropriate for Critical characteristics. Give careful consideration to defining Control Plan stages Prototype Pre-launch Production
  • 34.  
  • 35.
  • 36.
  • 37.
  • 38.
  • 39.
  • 40.
  • 41.
  • 42.
  • 43.  
  • 44.
  • 45.
  • 46.
  • 47.
  • 48.
  • 49.
  • 50.
  • 51.
  • 52.
  • 53. Quality Problems yes no no yes no yes no yes
  • 54.
  • 55.
  • 56. Update the PFMEA & Control Plans After the 8-D is completed, the PMEA and the control plan should be revised and updated as applicable Process Flow PFMEA Control Plan Work Instruction Scrap, Rework Data Warranty & Assembly Plant Data
  • 57.