askartsolutions logo- TS 16949

 

Understanding The ISO/TS 16949:2002 Standard 

5.4.2 Quality Management System Planning  

Top management shall: 

a)    Ensure QMS planning is carried out in order to meet clause 4.1 requirements as well as quality objectives 

b)    Maintain the integrity of QMS when changes to system are planned and implemented 

 

Key Explanation Points and Tips: 

Þ      It is the responsibility of top management to provide direction, resources and review for QMS planning.  

Þ      When developing your QMS process controls (for determining customer requirements, design, development, manufacture, delivery and customer support), you must focus on meeting customer and regulatory requirements as well as the planned QMS objectives established in clause 5.4.1. 

Þ      As I had mentioned earlier, clause 4.1 is the backbone of ISO 9001 as well as TS 16949. It provides direction on how to put together the framework of your QMS, i.e. your QMS plan.  The rest of the ISO and TS standard provide specific requirements for each of the (customer, support and management) processes that make up your QMS. 

Þ      Your QMS planning as per 4.1 requires you to identify all your QMS processes and describe each process and show their sequence and interaction with other processes. The criteria and methods for controlling these processes come from the rest of the ISO/TS requirements as well as your customer and your own organization. So if you have developed your QMS following the steps explained under clause 4.1, you have addressed clause 5.4.2a. 

Þ      The continuity and effectiveness of your QMS must be substantially maintained in the event of significant changes in your QMS or organization, e.g. management, ownership, relocation, technology, product, shift in customer base, etc. Changes must be carefully planned  so as not to disrupt your organizations ongoing capability and responsibility to effectively meet customer and regulatory requirements 

Þ      In such instances, change control would require:  

Þ       careful planning of the nature and timeline for the changes; 

Þ       determining the impact or outcome of such changes; 

Þ       ensuring adequate resources are available to implement the change; 

Þ       top management authorization  

Þ       change deployment and follow-up 

Þ       review of the QMS by top management after changes are effected.  

Þ      QMS planning could be a part of business planning or treated as an independent process depending on organizational structure and responsibilities. The management representative (see clause 5.5.2) typically facilitates QMS planning with the various process owners. The process owners must take responsibility for implementation, maintenance and improvement of their processes. The management representative may provide training and technical assistance as needed. Top management through business planning must provide leadership, resources and review of QMS performance. 

Þ      Performance indicators to demonstrate effective QMS planning could include – achievement of quality objectives; improved customer satisfaction ratings; reduced number and seriousness of internal/external audit nonconformities. 

 

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Preface - TS16949
◦ Introduction
◦ Major Clauses
◦ Process Approach -1
◦ Process Approach-2
◦ Plan/Do/Check/Act
◦ Cont Improve Model
◦ Compatibility
◦ TS 16949 Scope
◦ Application
◦ Normative References
◦ Terms And Definitions
◦ 4.1 General Reqmts
◦ 4.2.1 Documentation Reqmts
◦ 4.2.2 Quality Manual
◦ 4.2.3 Document Control
◦ 4.2.4 Control Of Records
◦ 5.1 Mgmt Commitment
◦ 5.2 Customer Focus
◦ 5.3 Quality Policy
◦ 5.4.1 Quality Objectives
◦ 5.4.2 QMS Planning
◦ 5.5.1 Quality Responsibility
◦ 5.5.2 Mgmtt Rep
◦ 5.5.3 Internal Communications
◦ 5.6 Mgmt Review
◦ 6.1 Resource Provision
◦ 6.2 Human Resources
◦ 6.3 Infrastructure
◦ 7.1 Planning Product Realization
◦ 7.2 Customer Processes
◦ 7.3.1 D & D Planning
◦ 7.3.2 D & D Inputs
◦ 7.3.2 D & D Outputs
◦ 7.3.4 To 7.3.6 - Review, Verification And Validation
◦ 7.3.6.2 Prototypes-PPAP-Changes
◦ 7.4.1 Supplier Mgmt
◦ 7.4.2 Purchasing Information And Supplier Performance Monitoring
◦ 7.5.1 Production Control-1
◦ 7.5.1 Production Control-2
◦ 7.5.2 Production Process Validation
◦ 7.5.3 to 7.5.5 Identification--Customer Property, etc
◦ 7.6 Monitoring And Measuring Devices
◦ 8.1 Measurement, Analysis & Improvement
◦ 8.2.1 Customer Satisfaction
◦ 8.2.2 Internal Audits
◦ 8.2.3 Monitoring Processes
◦ 8.2.4 Product Monitoring And Measurement
◦ 8.3 Control Of NC Product
◦ 8.4 Analysis Of Data
◦ 8.5.1 Continual Improvement
◦ 8.5.2 Corrective Action
◦ 8.5.3 Preventive Action
◦ TS 16949 Annex A - Control Plan