ts16949-2002 training

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    Awareness program onISO/TS16949:2002

    Technical Specification

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    ISO/TS 16949:2002

    It is an ISO Technical specification,aligns existing American (QS-9000),

    German (VDA6.1), French (EAQF) andItalian (AVSQ) automotive qualitysystems standards within the global

    automotive industry to eliminatevarious certifications for differentcustomers.

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    ISO/TS 16949:2002Was framedbyInternational Automotive

    Task Force (IATF)& Japan

    Automobile Manufacturers

    Association (JAMA).

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    Format of ISO/TS 16949:2002

    In the standard, Automotive qualitysystem requirements are written aroundthe format of ISO 9001:2000.

    ISO requirement

    TS requirement

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    Applicability ISO/TS 16949:2002

    Any organization in the automotivesupply chain is eligible for certification

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    The PDCA cycle

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    The PDCA cycle

    PLAN Establish the Objectives

    DO

    Implement the processes

    CHECK Monitor and measure theprocesses

    ACT Take actions to improvecontinually.

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    QUALITY MANAGEMENT SYSTEM

    4.1 General requirements

    4.2 Documentation requirements

    (Quality policy, Quality manual, Controlof documents (Engineeringspecification), Control of records

    (Record retention))

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    HIERARCHY OF QMSDOCUMENTATION

    Formats and Records

    Control plans,Docs, Work instructions

    QMS procedures

    Quality Manual

    Quality policy and Objectives

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    MANAGEMENT RESPONSIBILITY

    5.1 Management commitment (Processefficiency)

    5.2 Customer focus

    5.3 Quality Policy5.4 Planning (Quality objectives, QMS

    planning)

    5.5 Responsibility, Authority andcomn.(Resp & Authority,MR,CR)

    5.6 Management review (QMS

    performance, Review input, Output)

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    RESOURCE MANAGEMENT

    6.1 Provision of resources

    6.2 Human resources (Design skills,

    Training, Employee motivation)6.3 Infrastructure (Plant, facility,

    equipment, Contingency plans)

    6.4 Work environment (Personalsafety, Cleanliness of premises)

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    PRODUCT REALIZATION

    7.1 Planning of product realization7.2 Customer related processes (Specialchrs,Review requirements, feasibility

    review)7.3 Design and development (Productdesign, Process design)

    7.4 Purchasing (Approved suppliers,Purchasing info, verification, Incomingquality, Supplier monitoring)

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    PRODUCT REALIZATION

    7.5 Production and service provision(Control plan, Work instruction, Set upapproval, Maintenance, Tooling,Processvalidation, Traceability, Customerproperty)

    7.6 Control of measuring andmonitoring devices (MSA,Calibration,Laboratory)

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    MEASUREMENT, ANALYSIS ANDIMPROVEMENT

    8.1 General (SPC)

    8.2 Monitoring and measurement(Customer satisfaction, Internal audit

    Process, product audits, Measurement ofproduct, process, Layout inspection)

    8.3 Control of NC products

    8.4 Analysis of data

    8.5 Improvement (Processimprovement, CAPA)

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    BENEFITS OF QMSGreater focus on customer requirementsand Customer service.

    Conveys commitment to quality

    Continuous improvement cycle, results incost savings.

    Provides universal approach to quality

    and business.

    Controls process and systems andestablishes operational control.

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    BENEFITS OF QMSCorporate walls come down, peoplecommunicate better.

    Ensures product development and

    design changes are controlled.Creates awareness of the need oftraining

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    To summarize Internal benefits

    Management efficiency

    Planning

    Problem solvingSupplier control

    Communications

    Ability to changeDiscipline

    Staff morale

    Employee training

    Duplicate effort

    Re-work

    WasteCost

    Staff turn over

    Increases Reduces

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    To summarize External benefits

    Product and servicequality

    Customer satisfactionRepeat sales

    Company image

    Marketability

    Complaints

    Warranty claims

    Increases Reduces

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    Time for Questions?