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Understanding The ISO/TS 16949:2002 Standard 

5.3 Quality Policy  

Top management shall ensure that the quality policy:  

a)    is appropriate to the purpose of the organization 

b)    includes a commitment to comply with requirements and continually improve the effectiveness of the QMS 

c)    provides a framework to establish and review quality objectives 

d)    is communicated and understood within organization  

e)    is reviewed for continuing suitability 

 

Key Explanation Points and Tips: 

Þ      Developing a QMS must be a strategic business decision and therefore top management must provide the necessary direction and leadership, starting with establishing the quality policy and objectives. Your quality policy provides top management’s vision on quality management for the organization. It provides the organization with focused direction, i.e. high level goals and objectives for quality management.  

Þ      Your quality policy must be consistent with the scope of your QMS (see clause 1- scope) and other business, management and organizational strategies within the organization. Aggressive sales or marketing strategies must not be at the expense of quality management. 

Þ      Clause 4.1.a - requires that you document your quality policy and clause 5.3.c requires that you specify your commitment to ‘meet requirements’ and ‘continually improve the effectiveness of your QMS’. Clause 1 specifies requirements for the scope of your QMS. Paraphrasing the wording in clause 1 would be a good way to define your quality policy.  

Þ      The wording of the quality policy should preferably specify what requirements are being complied with (customer, regulatory, TS 16949, etc.). It must also clearly state the commitment to continually improve the effectiveness of the QMS. 

Þ      Beyond that, you may state other complementary and important policies (business growth; product or manufacturing technology; workforce competence; business flexibility, etc.)  

Þ      What you state in your quality policy, must lead to establishing quality objectives, e.g. if you state in your quality policy that you will “meet customer requirements”, then from this, you might derive customer focused objectives for – product defects; customer complaints and returns; on time delivery, etc. Similarly, “meet TS 16949 requirements”; from this you might derive process objectives for effectively and efficiently using TS requirements to manage, control and improve al of your QMS processes. 

Þ      Stating that you will “continually improve the effectiveness of your QMS” in your quality policy - can lead to a number of objectives, as your QMS is comprised of many processes and you could have one or more objectives to improve each process.  

Þ      Therefore, each statement in your quality policy may result in one or more quality objectives. These quality objectives do not need to be stated in your quality policy. Top management must clearly be involved in providing direction, establishing and reviewing these objectives. 

Þ      Earlier we had covered processes for internal and external communication. Your internal communication process should cover how the quality policy is communicated throughout the organization. There are many ways of doing this. Personnel must understand the importance and impact of the quality policy on the work they do.  

Þ      If you recall from 4.2.1 your QMS includes documented statements of your quality policy and quality objectives. Therefore, these documents must be controlled according to clause 4.2.3 control of documents. Your quality policy and quality objectives may be documented in your quality manual or as independent documents or both. 

Þ      If you recall from 4.2.1 your QMS includes the quality policy and quality objectives. Therefore, these are controlled documents and must be controlled according to clause 4.2.3 control of documents.  

Þ      The quality policy is not written in stone. It must be reviewed periodically by top management, for significant changes in your organization, e.g. management, ownership, relocation, product, shift in customer base, etc. Such changes may result in changes to the quality policy. The establishment of the quality policy should be part of the business planning or QMS planning processes. A review of the quality policy for continuing suitability should be part of your management review process (see clause 5.6).  

Þ      In clause 8.5.1, we will examine how the quality policy can be used as a tool for continual improvement. 

 

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


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