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IATF 16949 QMS Requirements Matrix

This document outlines the quality management system (QMS) for an organization adhering to ISO/TS 16949. It includes 4 levels of documentation: 1) topics at a high level, 2) procedures, 3) work instructions, and 4) forms. The QMS covers key areas such as organizational context, leadership and commitment, planning, resource management, competence, communication, document control, operational planning and control, customer requirements, design and development, and control of external providers. Forms, procedures, work instructions, flow diagrams and attachments are defined for each clause to ensure the various requirements of the QMS are met.

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100% found this document useful (5 votes)
6K views1 page

IATF 16949 QMS Requirements Matrix

This document outlines the quality management system (QMS) for an organization adhering to ISO/TS 16949. It includes 4 levels of documentation: 1) topics at a high level, 2) procedures, 3) work instructions, and 4) forms. The QMS covers key areas such as organizational context, leadership and commitment, planning, resource management, competence, communication, document control, operational planning and control, customer requirements, design and development, and control of external providers. Forms, procedures, work instructions, flow diagrams and attachments are defined for each clause to ensure the various requirements of the QMS are met.

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JOECOOL67
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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ISO/TS 16949 QMS - Manual-Procedures-Forms-Matrix -P-xxx Numbers

QMS Level 1 - Topic Level 2 Procedure Level 3 - Work Work instruction Level 4 Form Flow Diagram Flow Diagram Name Attachment Attachment
Clause Procedure Name Instruction Name Form # Name # Name

All Quality Management System - Quality Manual - QM-016

4 Context of the organization P-400 Organizational context F-440-001 QMS-Process identification worksheet
F-440-002 Organizational context worksheet
F-440-003 Product safety worksheet
FD-440-001 Process interaction flow diagram

5 Leadership P-500 Leadership


FD-510-001 Business process map
A-510-001 Corporate responsibility policies
A-520-001 Quality policy
A-530-001 Organization chart

6 Planning for the Quality Management System P-600 Planning for the Quality Management System F-610-001 Risk and opportunity worksheet
F-612-001 Contingency plans worksheet
F-620-001 Quality objectives planning record A-600-001 PDCA guidelines

P-612 Preventive action

7.1 Resources P-710 Resource management F-710-001 Equipment problem report


F-710-002 Resource maintenance record

7.1.5 Monitoring and measuring resources P-715 Control of monitoring and measuring equipment F-715-001 Equipment calibration list A-715-001 Calibration activities and records guidelines
F-715-001 Laboratory requirements worksheet

7.2 Competence P-720 Competence and awareness F-720-001 Training action plan
7.3 Awareness F-720-002 Group training record
F-720-003 Job description
F-720-004 Employee training summary
F-720-005 Auditor competency worksheet

7.4 Communication P-740 Communication F-740-001 Comment and suggestion report

7.5 Documented information P-750 Control of documented information WI-750-001 Document numbering system F-750-001 List of documented information
F-750-002 Records matrix
F-750-003 Master documentation lists
F-750-004 Quality records table
F-750-005 Document change request form
F-750-006 Document revision checklist
F-750-007 Software inventory spreadsheet

8.1 Operational planning and control P-810 Operational planning and control F-810-002 Project planning worksheet FD-810-002 Process flow diagram

8.2 Determination of requirements for products and services P-820 Customer related processes F-820-001 Client assessment report
F-820-002 Production order

8.3 Design and development of products and services P-830 Design and development of products F-830-001 Design plan
F-830-002 Design review record
F-830-003 Design change form

P-831 Design and development of manufacturing processes

8.4 Control of externally provided products and services P-840 Control of external providers F-840-001 Provider assessment report
F-840-002 List of acceptable sources
F-840-003 Provider corrective action request - PCAR
F-840-004 Purchase requisition
F-840-005 Purchase order
F-840-006 Business agreement - contract

8.5.1 Control of production and service provision P-851 Control of production


F-851-001 Process routing sheet - summary FD-850-001 Operations-Production and Service
F-851-002 Process routing sheet - summary
F-851-003 Process validation worksheet
F-851-006 External property control log
F-851-010 Control plan worksheet

P-857 Other operational control F-857-001 Service projects log


F-857-002 Project inspection completion report

P-860 Release of products and services

8.5.2 Identification and traceability P-852 Identification and traceability F-852-001 Identification tag
F-852-002 Traceability serial number log
F-852-003 Traceability label

8.5.4 Preservation P-854 Preservation F-854-001 Storage inspection report


F-854-002 Packing slip / Invoice

8.7 Control of nonconforming outputs P-870 Control of nonconforming outputs F-870-001 Nonconformance report - NCR

9.1 Monitoring, measurement, analysis, and evaluation P-910 Monitoring, measurement, analysis and evaluation F-910-001 Production-Monitoring, measuring, and analysis table
F-910-002 QMS-Monitoring, measuring, and analysis table
F-910-004 Inspection report

P-911 Statistical techniques F-911-001 Frequency distribution report

P-913 Root cause analysis F-913-001 Root cause analysis action plan

9.1.2 Customer satisfaction P-912 Customer satisfaction F-912-001 Customer survey and analysis

9.2 Internal audit P-920 Internal audit F-920-001 Applicable procedure by work area
F-920-002 Internal audit checklist
F-920-003 Audit plan
F-920-004 Audit report

9.3 Management review P-930 Management review F-930-001 Management review agenda
F-930-002 Management review output report

10.1 General P-1010 Improvement F-1010-001 Data analysis worksheet

10.2 Nonconformity and corrective action P-1020 Nonconformity and corrective action F-1020-001 Corrective action request - CAR

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