Professional Documents
Culture Documents
Clause References : 4.3.2 , 4.4.1.2 , 6.3 , 7.1.3.1 , 7.5.3.2.2 , 8.1.2 , 8.2.3.1.3 , 8.3.3.2 , 8.3.3.3 , 8.3.4.4 , 8.3.5.2 ,8.5.1.1 , 8.5.6 , 10.2.4 & 10.2.5 Date:
Auditor: Auditee:
1 Are project authorisations being received from Management for all projects
Is process available for new product development which ensures quality planning, project planning, quality or
3
control plans ?
5 Does APQP timing plan available for the new product development ?
6 Is the quality planning process consistent with all other requirement of QMS?
Are customer requirements and reference to it's technical specifications including in APQP or product
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realization process?
8 Is acceptance criteria defined for the product being developed and where required approved by the customer?
13 Are DFMEA carried out for all parts and proto control plan made
14 Are design review performed for Fit, Form & Function (if proprietary)?
15 Are the changes verified, validated & results recorded before implementation?
17 Is feasibility review conducted for ability to supply product as per customer requirement?
18 Have project team made with CFT formation with the consent of all functional head
Is product Design & Development Plan available and covers design and development stages, reviews,
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verification & validation, responsibility & authority, target dates etc?
Is multidisciplinary approach utilized for developing & finalizing special characteristics, review of FMEAs,
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development & review of control plans ?
21 Is process available for design & development input ?
25 Have risk assessment carried out by management and re authorisation made on product development
26 Are inputs related to products like fit, form, function, applicable statutory &
27 Is process available for design & development output ?
28 Are design output verified against design input prior to design release ?
Are design output provides appropriate information for purchasing, production with acceptance criteria and
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product characteristics essential for it's safe & proper use?
33 What is the frequency to review the follow up of the actions decided during review?
35 Are prototype programme & control plan available when required by customer?
36 Are performance testing activities monitored as per timing plan & conformity to the requirements?
Are the design changes identified, reviewed, verified, validated and approved before implementation and
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relevant records Maintained?
38 Are customer approval obtained for parts through PSW/customer letter
41 8D Analysis is reviewed & for every 8D cause of non detection & cause of occurrence identified ?
How do you check the effectiveness of correcticve action ?Are all relevant documents updated for change
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/CAPA?
Have to analyze warranty data based on claim month, production month, dealer wise & Km wise etc. on monthly
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basis.
Have to carry out the NTF analysis and initiate actions to achieve the target, so that the troubles faced by the
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final consumer are understood correctlyand recurrence of complaints by final consumer are prevented.
45 Have to create the list of lessons learned to apply during new product development
SCORE: 0
4 Excellent
0 No system -Major NC
Doc No.: XXX/XXX/XX | Rev No.: XX Prepared By: Mr.Name Sheet Author: Mr.Name
Rev Date: XX.XX.XXXX Approved By: Mr.Name Page No.: 1 of 1.