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APQP Matrix

The document outlines the APQP Responsibility Matrix, detailing the development activities and responsibilities for new products, engineering changes, and process changes. It specifies the overall responsibility of the Engineering Head and categorizes tasks into phases, with corresponding responsibilities assigned to various departments. The matrix serves as a guideline for managing product development and ensuring accountability throughout the process.

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0% found this document useful (0 votes)
382 views1 page

APQP Matrix

The document outlines the APQP Responsibility Matrix, detailing the development activities and responsibilities for new products, engineering changes, and process changes. It specifies the overall responsibility of the Engineering Head and categorizes tasks into phases, with corresponding responsibilities assigned to various departments. The matrix serves as a guideline for managing product development and ensuring accountability throughout the process.

Uploaded by

SHI QUALITY
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as XLSX, PDF, TXT or read online on Scribd
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Format No : FO -NP20

APQP Responsibility Matrix Rev No: 0


Rev Date :01.07.2022

Purpose : To define the category of development activities & responsibilities

Scope : This WI is applicable for development of new product,Engg change and any Process change of existing items or any similar component, RM, Supplier change, Location Change

Responsibility : Overall responsibility is Engineering Head


CATEGORY FOR APQP LEGEND
A New Part ( no experienced so far ) = Activity to be done
B New part (Similar component) Blank Activity not required
C ECN/PCN c Prime Responsibility
D Plant Location Change ∆ Secondary responsibility
E Supplier Change
F Raw Material Change
* Additional points may be considered based on industry specific requirement
CATEGORY Responsible Department
S.No. Description Critical DOCUMENT REFERENCE
A B C D E F MKT NPD QA PROD PUR HR MNT T.M
Phase 1 : Plan & Define program
Request for Quotation along with Drawing & recording in
1.1
enquiry register = = = c ∆ Enquiry register & Drawing

1.2 CFT Formation = = = = = = c Timing plan

1.3 Study the Drawing / Enquiry received from Customer and


cust. Spec. Requirement * = = = = ∆ c ∆ ∆ Baloon drawing & Drawing
study

1.4 Listing of Special Product and Process characterstic = = = c ∆ List of special characteristics

Clarification from customer for incomplete


1.5
information/Deviation = = = = ∆ c ∆ ∆ Drawing study/Mail

1.6 Review Past Defect History/Lessons Learned of similar part * = = = = = = ∆ c ∆ ∆ Lessons learned from past

1.7 Feasibility Study = = = = = ∆ c ∆ ∆ ∆ ∆ ∆ ∆ Feasibility Study


1.8 Cost Estimation and Submission of Quotation = = = = = c ∆ ∆ ∆ Quotation
1.9 Receipt of LOI/PO/mail confirmation = = = = c ∆ PO/mail confirmation
Phase 2 : Product Design & Development
2.1 Preparation of APQP Timing Plan and approval for Top
Management * = = = = = = ∆ c ∆ ∆ ∆ ∆ ∆ APQP Timing Plan

2.2 Preliminary Process flow diagram, Prototype Control Plan = c ∆ ∆ ∆ PFC, Control Plan

2.3 Prepare Prototype sample = c ∆ ∆ ∆


2.4 Prototype sample submission = ∆ c

2.5 Sample Approval from Customer = c ∆


2.6 Follow-up from Customer if no response within a week = c ∆
2.7 Prepare Micro level Die/Tool Development plan * = = = c ∆ ∆ ∆ ∆ Tool Development Plan
2.8 Prepare Micro Level Gauge/Fixture Development Plan * = = = c ∆ ∆ ∆ Gauge/Fixture development
plan
2.9 Supplier Development Plan * = = = = = ∆ c c Supplier Development Plan
Phase 3 : Process Design and Development
3.1 Prepare Process flow chart = = = c ∆ ∆ PFC
3.2 Prepare PFMEA Matrix = = = ∆ c ∆ ∆ ∆ PFMEA Matrix
3.3 PFMEA preparation * = = = = = ∆ c ∆ ∆ ∆ ∆ PFMEA
3.4 Preparation of Prelaunch Control Plan = = = = c ∆ ∆ Pre launch CP
Preparation of WI, Operation standard and Inspection
3.5
Standard = = = = c ∆ WI/SOP/inspection standard

3.6 T1 Trial * = = = = = c ∆ ∆ ∆ Try out report/Prod record


3.7 Sample submission * = = = = = ∆ c ∆ Layout report
3.8 Sample Approval from Customer = = = = = c ∆ ∆ Customer approval evidence
3.9 Follow-up from Customer if no response within a week = = = = = c ∆ ∆
3.10 T2 Trial ( If Req ) * = = = = = c ∆ ∆ ∆ Try out report/Prod record
3.11 Sample submission * = = = = = ∆ c ∆ Layout report
3.12 Sample Approval from Customer = = = = = c ∆ ∆ Customer approval evidence
3.13 Follow-up from Customer if no response within a week = = = = = c ∆ ∆
3.14 T3 Trial ( If Req…. And So on ) * = = = = = c ∆ ∆ ∆ Try out report/Prod record
3.15 Sample submission * = = = = = ∆ c ∆ Layout report
3.16 Sample Approval from Customer = = = = = c ∆ ∆ Customer approval evidence
3.17 Follow-up from Customer if no response within a week = = = = = c ∆ ∆
3.18 Preparation and Display of Packing Standard = = = ∆ c ∆ ∆ Packing Standard
3.19 MSA and SPC Plan = = = = c ∆ ∆ MSA & SPC Plan
Phase 4 : Product and Process Validation
4.1 Training to concerned supervisor, operator and inspector * = = = = = ∆ ∆ c ∆ ∆ Training attendance record

4.2 Supplier PPAP audit and approval * = = = = = ∆ c ∆ Supplier PPAP

4.3 Pilot lot preparation with inspection report * = = = = = = c ∆ ∆ Layout/Set up/patrrol


4.4 Product & Process audit = = = = = = ∆ c ∆ Process product audit report
4.5 Preliminary Process capability study * = = = = = = ∆ c ∆ SPC report
4.6 Preliminary Measuring System Analysis = = = = = = ∆ c ∆ MSA report
4.7 Prepare all PPAP documents, including PSW. = = = = = = c ∆ ∆ PSW

4.8 Submit pilot lot & PPAP documents to customer for


approval. * = = = = = = c ∆ ∆ ∆ PPAP documents

Follow up with customer if no response is received within a


4.9
week = = = = = = c ∆
4.10 Preparation of Production control plan = = = = = c ∆ ∆ Control plan
Phase 5 : Feedback Assessment & Corrective Action

5.1 Compilation of Quality Problem during trial and pilot lot in


PDCA Analysis Summary Sheet (PDCA Format) * = = = = = = c ∆ ∆ PDCA Sheet

5.2 Past defect history to be finalized = = = = = = c ∆ ∆ Past Defect History


5.3 Start of initial production control * = = = = = = c ∆ ∆
5.4 APQP Signoff after SOP at customer end = = = = = = ∆ c ∆ ∆ ∆ ∆ ∆ APQP Sign Off

Prepared By: Approved By:

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