askartsolutions logo- TS 16949

 

Understanding The ISO/TS 16949:2002 Standard

Introduction

0.1 General:

The adoption of a QMS should be a strategic decision for your organization. Various factors influence the design and implementation of your QMS. These include – varying needs; particular objectives; products provided; processes employed and size and structure of the organization. The ISO 9001 standard does not require uniformity of QMS structure or documentation.  

The QMS requirements specified in ISO 9001 are complementary to requirements for product. Information marked “Note” is for guidance in understanding or clarifying the requirement. 

This international standard can be used by internal and external parties, including certification bodies, to assess an organization’s ability to meet customer, regulatory and the organization’s own requirements. 

The quality management principles stated in ISO 9000 and ISO 9004 have been taken into consideration in developing this standard. 

Key Explanation Points and Tips:

Þ     The purpose of an organization is to identify and meet the needs and expectations of its customers and other stakeholders and gain competitive advantage. One of the strategies it might use to achieve this goal is to continually improving the effectiveness and efficiency of its capabilities.  

Þ     ISO 9001:2000 is a powerful business tool that organizations may use to achieve this.  Organizations use ISO 9001 to achieve goals and objectives related to meeting customer and regulatory requirements and enhancing customer satisfaction. 

Þ     TS 16949:2002 is built upon all of the requirements, principles and concepts included in ISO 9001, and goes further in specifying additional and supplemental requirements that are specific to the automotive sector. We will continue with our introductory review of ISO 9001 concepts and principles before we get into the details of TS 16949 requirements.  

Þ     While the focus is on quality management, the ISO 9001 business model may be applied just as well to manage the entire organization. The standard embodies business concepts and principles universally recognized and applied for sound business management. As such, ISO 9001 should be used as a strategic business management tool.  

Þ     The ISO 9001 standard defines a generic set of requirements for all organizations, regardless of size, complexity or industry sector. These requirements define controls for your quality management system that focus on continually improving the effectiveness of your QMS in meeting customer requirements and thus enhancing customer satisfaction. 

Þ    It is important to note that the ISO 9001 standard does not specify requirements for product. The focus of all ISO 9001 requirements is on your QMS and its processes. By effectively controlling and continually improving your QMS processes, there will obviously be a positive impact on product quality performance and conformity to customer requirements. 

Þ    You must ensure that the scope of your QMS addresses all customer requirements. Customer requirements may show up in contracts, blueprints, their supplier quality manuals, or referenced to applicable industry and regulatory standards and codes, etc. 

Þ    It is important to state here that ISO 9001 certification must not be the ultimate goal of QMS implementation. Your constant goal must be to continually improve the effectiveness and efficiency of the organization for the benefit of all its stakeholders. Obtaining certification must be considered as just a stepping stone in this journey. Organizations that understand and follow this approach will get the most benefit from QMS development and implementation. 

Þ     Organizations implementing an ISO 9001 based QMS must conform to all applicable requirements that the standard specifies. This provides internal and external parties (customers, registrars and regulatory bodies), the basis (i.e. a benchmark) against which to assess the organizations ability to meet customer, regulatory and internal requirements.  

Þ    It is now a common practice to use ISO 9001 certification as a requirement for making contractual decisions. The automotive OEM’s (subscribing to the TS 16949 standard) require their direct (tier 1) suppliers of manufactured product and related services to obtain TS 16949 certification. Tier 1 suppliers in turn are required to flow down conformity to TS 16949 requirements through supplier QMS development. 

Þ     QMS design and implementation will vary from organization to organization. ISO 9001 allows this flexibility because organizations may have differing - goals and objectives; business risks; range and complexity of products; processes and resources; organizational size and structure; workforce competence and stability; etc. This flexibility may relate to QMS scope; structure; documentation or application of ISO 9001 requirements. 

Þ     Personnel performing QMS assessments must - have adequate training on the requirements of the ISO 9001 standard and auditing practices as defined by ISO 19011; be familiar with your QMS, customer requirements and applicable regulatory requirements. 

The guidance documents ISO 9000 and ISO 9004 provide the eight quality management principles  on which this standard is based. These are: 

 

Principle 1  Customer-Focus 

Your organization depends on customers and therefore your organization should understand current and future customer needs, meet customer requirements and strive to exceed customer expectations (see clause 5.2; 7.2; and 8.2.1). 

 

Principle 2  Leadership    

Leaders establish unity of purpose and direction of the organization. They should create and maintain the internal environment in which people can become fully involved in achieving the organization's objectives (see clause 5) 

 

Principle 3  Involvement of People 

People at all levels are the essence of an organization and their full involvement enables their abilities to be used for the organization’s benefit (see clause 6.2). 

 

Principle 4 — Process Approach   

A desired result is achieved more efficiently when related resources and activities are managed as a process (see clause 4.1). 

 

Principle 5  System Approach to Management 

Identifying, understanding and managing interrelated processes as a system contributes to the organization’s effectiveness and efficiency in achieving its objective (see clause 4.1).. 

 

Principle 6 —  Continual Improvement 

Continual improvement of the organizations overall performance should be a permanent objective of the organization (see clause 8.5.1 and 4.1). 

 

Principle 7 — Factual approach to decision making   

Effective decisions are based on the analysis of data and information (see clause 4.1e and 8.4). 

 

Principle 8  Mutually beneficial supplier relationships 

An organization and its suppliers are interdependent, and a mutually beneficial relationship enhances the ability of both to create value (see clause 7.4). 

 

Þ     These eight management principles form the basis for all QMS standards within the ISO 9000 family which includes TS 16949:2002. All of these principles are included as requirements in one or more clauses of the TS 16949 standard. 

 

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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