Unique TL9000 Requirements

 
This reference is a quick clause-by-clause summary of the ISO/TS 16949:2002 requirements. The additional ISO/TS 16949:2002 clauses are highlighted by the asterisks in the TS column.

Note: See the actual standard for a complete description of the requirements.

ISO/TS 16949:2002 Clauses

TS

Summary of Requirements

4. Quality Management System

 

 

4.1 General Requirements

 

Implement quality system and continually improve it

4.1.1 General Requirements -Supplemental

*

Remain responsible for any outsourced processes

4.2 Documentation Requirements

 

 

4.2.1 General

 

Include the required documents and records

4.2.2 Quality Manual

 

Establish and maintain a quality manual

4.2.3 Control of Documents

 

Ensure documents are at right status in right places

4.2.3.1 Engineering Specifications

*

Conduct timely review of customer specifications

4.2.4 Control of Records

 

Identify records and keep as evidence of conformity

4.2.4.1 Records Retention

*

Control records for customer and legal requirements

5. Management Responsibility

 

 

5.1 Management Commitment

 

Show evidence of top management commitment

5.1.1 Process Efficiency

*

Review processes for efficiency and effectiveness

5.2 Customer Focus

 

Meet the requirements and satisfy your customers

5.3 Quality Policy

 

Have top management express quality intentions

5.4 Planning

 

 

5.4.1 Quality Objectives

 

Set measurable targets for products and processes

5.4.1.1 Quality Objectives -Supplemental

*

Define measurements for business plan

5.4.2 Quality Management System Planning

 

Carry out plans for quality system and its processes

5.5 Responsibility, Authority, and Communication

 

 

5.5.1 Responsibility and Authority

 

Make sure everyone knows their duties and roles

5.5.1.1 Responsibility for Quality

*

Staff every production shift with quality coordinator

5.5.2 Management Representative

 

Appoint a manager as focal point for quality system

5.5.2.1 Customer Representative

*

Assign representative for customer requirements

5.5.3 Internal Communications

 

Keep everyone informed of system effectiveness

5.6 Management Review

 

 

5.6.1 General

 

Review the quality system at planned intervals

5.6.1.1 Quality Management System Performance

*

Include quality objectives and cost of poor quality

5.6.2 Review Input

 

Ensure the required agenda topics are covered

5.6.2.1 Review Input -Supplemental

*

Analyze field failures and their impact on quality

5.6.3 Review Output

 

Record the decisions and actions from reviews

6. Resource Management

 

 

6.1 Provision of Resources

 

Provide necessary resources to meet requirements

6.2 Human Resources

 

 

6.2.1 General

 

Ensure everyone working in system is competent

6.2.2 Competence, Awareness, and Training

 

Train personnel and recognize their contributions

6.2.2.1 Product Design Skills

*

Ensure product designers are skilled and competent

6.2.2.2 Training

*

Maintain documented training procedures

6.2.2.3 Training on the Job

*

Provide OJT for new or revised jobs affecting quality

6.2.2.4 Employee Motivation and Empowerment

*

Motivate employees to meet objectives and improve

6.3 Infrastructure

 

Provide facilities, equipment, and support services

6.3.1 Plant, Facility, and Equipment Planning

*

Evaluate the effectiveness of existing operations

6.3.2 Contingency Plans

*

Prepare contingency plans in event of an emergency

6.4 Work Environment

 

Manage combination of human and physical factors

6.4.1 Personnel Safety to Achieve Product Quality
*
Address product safety and risks to employees
6.4.2 Cleanliness of Premises
*
Maintain premises in state of order and cleanliness

7. Product Realization

 

 

7.1 Planning of Product Realization

 

Plan and develop processes for product realization

7.1.1 Planning -Supplemental

*

Consider customer requirements in quality plans

7.1.2 Acceptance Criteria

*

Define acceptance criteria

7.1.3 Confidentiality

*

Ensure confidentiality of customer products

7.1.4 Change Control

*

Control changes that impact product realization

7.2 Customer-Related Processes

 

 

7.2.1 Determination of Product Requirements

 

Define customer, regulatory, and own requirements

7.2.1.1 Customer-Designated Special Char.

*

Demonstrate conformity for special characteristics

7.2.2 Review of Product Requirements

 

Review requirements before committing to customer

7.2.2.1 Review -Supplemental

*

Waiver of review requires customer authorization

7.2.2.2 Organization Manufacturing Feasibility

*

Confirm and document manufacturing feasibility

7.2.3 Customer Communication

 

Talk to customers about products and complaints

7.2.3.1 Customer Communication -Supplemental

*

Communicate in customer format, e.g. CAD, EDI

7.3 Design and Development

 

 

7.3.1 Design and Development Planning

 

Plan design stages, activities, and responsibilities

7.3.1.1 Multidisciplinary Approach

*

Involve appropriate functions in planning process

7.3.2 Design and Development Inputs

 

Identify and review input requirements for design

7.3.2.1 Product Design Input

*

Document and review product design inputs

7.3.2.2 Manufacturing Process Design Input

*

Document and review mfg. process design inputs

7.3.2.3 Special Characteristics

*

Include all special characteristics in control plan

7.3.3 Design and Development Outputs

 

Prepare design outputs and approve before release

7.3.3.1 Product Design Outputs -Supplemental

*

Express for V&V of product design

7.3.3.2 Manufacturing Process Design Output

*

Express for V&V of manufacturing process design

7.3.4 Design and Development Review

 

Review ability of design results to meet requirements

7.3.4.1 Monitoring

*

Report measurements at design stages

7.3.5 Design and Development Verification

 

Verify the design outputs meet input requirements

7.3.6 Design and Development Validation

 

Validate the product is okay for application or use

7.3.6.1 Validation -Supplemental

*

Perform validation per customer requirements

7.3.6.2 Prototype Program

*

Include prototype program, if required by customer

7.3.6.3 Product Approval Process

*

Use approval procedure recognized by customer

7.3.7 Control of Design and Development Changes

 

Review, verify, and validate any design changes

7.4 Purchasing

 

 

7.4.1 Purchasing Process

 

Evaluate, select, monitor, and control your suppliers

7.4.1.1 Regulatory Conformity

*

Use products conforming to applicable regulations

7.4.1.2 Supplier QMS Development

*

Develop suppliers with goal of conformity to TS

7.4.1.3 Customer-Approved Sources

*

Purchase from approved sources, if in contract

7.4.2 Purchasing Information

 

Create purchase orders describing supplier products

7.4.3 Verification of Purchased Product

 

Check purchases to ensure they meet requirements

7.4.3.1 Incoming Product Quality

*

Assure quality by one or more of accepted methods

7.4.3.2 Supplier Monitoring

*

Monitor supplier performance

7.5 Production and Service Provision

 

 

7.5.1 Control of Production and Service Provision

 

Plan and control production and service activities

7.5.1.1 Control Plan

*

Develop control plans and update for changes

7.5.1.2 Work Instructions

*

Document work instructions and make accessible

7.5.1.3 Verification of Job Setups

*

Make work instructions available for setup personnel

7.5.1.4 Preventive and Predictive Maintenance

*

Implement a total preventive maintenance system

7.5.1.5 Management of Production Tooling

*

Implement system for managing production tooling

7.5.1.6 Production Scheduling

*

Schedule production to meet customer requirements

7.5.1.7 Feedback of Information from Services

*

Establish process to communicate service concerns

7.5.1.8 Service Agreement with Customer

*

Verify service effectiveness, if agreement exists

7.5.2 Validation of Production & Service Processes

 

Examine the process if you can’t check the product

7.5.2.1 Validation -Supplemental

*

Apply to all production and service processes

7.5.3 Identification and Traceability

 

Identify the product and its inspection and test status

7.5.3.1 Identification & Traceability -Supplemental

*

Apply traceability in all cases

7.5.4 Customer Property

 

Exercise care with any customer property

7.5.4.1 Customer-Owned Production Tooling

*

Permanently mark all customer-owned tooling

7.5.5 Preservation of Product

 

Handle, store, package, and protect the product

7.5.5.1 Storage and Inventory

*

Assess product condition in stock at planned interval

7.6 Control of Monitoring and Measuring Devices

 

Calibrate measuring equipment for valid results

7.6.1 Measurement Systems Analysis

*

Conduct statistical studies to analyze variation

7.6.2 Calibration/Verification Records

*

Include required items in the calibration records

7.6.3 Laboratory Requirements

*

 

7.6.3.1 Internal Laboratory

*

Define scope for capability of own internal laboratory

7.6.3.2 External Laboratory

*

Use accredited lab or one approved by customer

8. Measurement, Analysis, and Improvement

 

 

8.1 General

 

Plan, measure, analyze, and improve processes

8.1.1 Identification of Statistical Tools

*

Determine needed tools and include in control plan

8.1.2 Knowledge of Basic Statistical Concepts

*

Understand variation, stability, and over adjustment

8.2 Monitoring and Measurement

 

 

8.2.1 Customer Satisfaction

 

Ask customers what they think about your products

8.2.1.1 Customer Satisfaction - Supplemental

*

 

8.2.2 Internal Audit

 

Evaluate conformity and effectiveness of system

8.2.2.1 Quality Management System Audit

*

Audit system for conformity to TS requirements

8.2.2.2 Manufacturing Process Audit

*

Audit each manufacturing process for effectiveness

8.2.2.3 Product Audit

*

Audit products at stages of production and delivery

8.2.2.4 Internal Audit Plans

*

Include all processes and shifts in annual plan

8.2.2.5 Internal Auditor Qualification

*

Ensure auditors are qualified to audit TS

8.2.3 Monitoring and Measurement of Processes

 

See if processes are achieving planned results

8.2.3.1 M & M of Manufacturing Processes

*

Perform studies on new manufacturing processes

8.2.4 Monitoring and Measurement of Product

 

Verify products meet acceptance criteria

8.2.4.1 Layout Inspection and Functional Testing

*

Perform for each product in control plan

8.2.4.2 Appearance Items

*

Provide, maintain, and control appearance masters

8.3 Control of Nonconforming Product

 

Prevent use or delivery of nonconforming product

8.3.1 Control of NC Product -Supplemental

*

Classify unidentified or suspect product as NC

8.3.2 Control of Reworked Product

*

Make rework and re-inspection instructions available

8.3.3 Customer Information

*

Promptly inform customer if NC product is shipped

8.3.4 Customer Waiver

*

Seek waiver if process different than approved

8.4 Analysis of Data

 

Analyze effectiveness and identify improvements

8.4.1 Analysis and Use of Data

*

Compare performance trends to quality objectives

8.5 Improvement

 

 

8.5.1 Continual Improvement

 

Continually improve effectiveness of quality system

8.5.1.1 Continual Improvement of Organization

*

Define a process for continual improvement

8.5.1.2 Manufacturing Process Improvement

*

Focus on reduction of product and process variation

8.5.2 Corrective Action

 

Fix detected problems and prevent recurrence

8.5.2.1 Problem Solving

*

Use defined process for problem solving

8.5.2.2 Error-Proofing

*

Use error-proofing in corrective action process

8.5.2.3 Corrective Action Impact

*

Apply actions to similar processes and products

8.5.2.4 Rejected Product Test/Analysis

*

Analyze rejected parts and act to prevent recurrence

8.5.3 Preventive Action

 

Avoid potential problems by preventing occurrence

About the Author

Larry Whittington is President of Whittington & Associates, a quality system training, consulting, and auditing company located in Marietta, Georgia. He is an ASQ Certified Software Quality Engineer and Quality Auditor. Both the RAB and IRCA have certified him as an ISO 9000 Lead Auditor. He is also a trained TickIT Lead Auditor for software systems and a certified QS-9000 Lead Auditor for the automotive industry. Mr. Whittington can be contacted at 770-517-7944, by e-mail at Larry@WhittingtonAssociates.com.

 
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