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    Audit Contract VDA 6.3-2010

    Client: (z.B. management,person responsible for the product, person responsible for the auditprogramme)

    Audited Party: (z.B. internal department, supplier)

    Reason for Audit:

    Audit Objective:

    Audit Variant:

    Internal Audit Potential Analysis

    External Audit Special Audit

    Audit Location:

    Internal Audit external

    Audit Team:

    Lead Auditor:

    Auditors:

    Audit Extent:

    Prosesses: Products:

    Manufacturing

    Locations: Interfaces:

    Outside Processes:

    Process Specialist(s):

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    VDA 6.3-2010 Audit Report: Assessment of Quality Cabability

    Supplier: Client: Date:Supplier No.: Reason for contract: Contract No.:

    Location:

    Process/ProductAssess-ment

    indexAchieved Classified Findings / requirements

    Overall Process P2 bis P7 EG nb

    ED nb

    EP nb

    Product Group*

    EPN nb

    EPN nb

    EPN nb

    EPN nb

    EPN nb

    * Values automaticly taken from Assessment Matrix

    Classification scale: A: 90-100% (Q-cabable); B: >= 80-90% (conditionally Q-cabable); C:

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    Explanations

    Supplier: Client: Date:

    Participants: Auditor:

    The improvement program was discussed in the final meeting on site and handed over as a draft.. The audited Organisaion is asked to define sustainable corrective actions for the identified wea

    implement them rapidly.

    We point out that within the audit the processes only can be checked randomly. Other weak points and / or potentials for imprevement may be possible.

    It is the responsibility of the audited parties to expand the investigation and necessary measures to similar areas / issues.

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    VDA 6.3-2010 Audit Report: Assessment of Quality Cabability

    Supplier: Client:

    Assessment Elements / Process Stages Assessment after Process Analysis (mean value,generic base

    Target

    Minimum requirement 80 90 Minimum requirement

    per assessment element per assessment element

    Assessment elements /

    Process stages

    pre-

    audit actual

    Assessment elements /

    Process stages

    pre

    audit actual

    Project ManagementP 2 nb

    Process input

    EU 1 nbPlanning Product/Process

    P 3 nb

    Process sequence

    EU 2 nb

    Carrying out

    Product/Process P 4 nb

    Personnel support

    EU 3 nb

    Supplier Management

    P 5 nb

    Material resources

    EU 4 nb

    Prozess Analysis

    P 6 nb

    Proces effectiveness level

    EU 5 nb

    Customer Satisfaction

    P 7 nb

    Process result

    EU 6 nb

    Process Name 1 E 1 nb

    Transport / parts handling

    / storage EU 7 nb

    Process Name 2 E 2 nb Generic Baseline

    Process Name 3 E 3 nb Process responsiblity PR nb

    Process Name 4 E 4 nb Target orientation TO nb

    Process Name 5 E 5 nb Communication CO nb

    Process Name 6 E 6 nb Risk orientation RI nb

    Process Name 7 E 7 nb

    Process Name 8 E 8 nb Overall Compliance EG nb

    B f SOP

    Erfllungsgrad

    Assignment to

    Product group

    Erfllungsgrad

    Produktgruppe1

    Produktgruppe2

    Produktgruppe3

    Produktgruppe4

    Produktgruppe5

    70 80 90 100 660

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    VDA 6.3-2010 Assessment Matrix including Product Groups

    Supplier: Client:A Development

    P 2 Project Management

    2.1 2.2* 2.3 2.4 2.5* 2.6 2.7*

    nb nb nb nb nb nb nb

    P 3 Planning Product/Process Development

    Product Process

    3.1 3.2* 3.3 3.4 3.5 3.1 3.2* 3.3 3.4 3.5

    nb nb nb nb nb EPdP nb nb nb nb nb

    P 4 Carrying out Product/Process Development

    Product Process

    4.1 4.2 4.3 4.4 4.5* 4.6 4.7 4.8 4.9 4.1 4.2 4.3 4.4 4.5* 4.6 4.7 4.8 4.9

    nb nb nb nb nb nb nb nb nb EPdR nb nb nb nb nb nb nb nb nb

    B Full Production

    5.1* 5.2 5.3 5.4* 5.5* 5.6 5.7

    P 5 Supplier Management nb nb nb nb nb nb nb

    P 6 Process Analysis Serial Production

    6.1.1* 6.1.2 6.1.3 6.1.4 6.1.5 6.2.1* 6.2.2 6.2.3* 6.2.4* 6.2.5 6.2.6 6.3.1 6.3.2* 6.3.3 6.4.1 6.4.2* 6.4.3 6.4.4 6.5.1 6.5.2 6.5.3* 6.5.4*

    Process step 1:

    nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb

    Process step 2:

    nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb

    Process step 3:

    nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb

    Process step 4:

    nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb nb

    nb

    nb

    Entry: only following values are allowed

    nb not assessed

    10 Requirements fully satisfied

    8 Requirements mainly satisfied

    6 Requirements partly satisfied

    4 Requirements inadequately satisfied

    0 Requirements not satisfied

    1 Process Input 2 Work Content / Process Sequences 3 Personnel Support 4 Material Ressources5 Process Effectiveness

    Level

    Process Name 1

    Process Name 2

    Process Name 3

    Process Name 4

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    Date:

    Supplier: Client:

    Pos.

    Quest

    Nr.

    QuestionPionts Comments / Assesment Remarks

    A Development

    P 2 Project Management

    2.1 Is the project organisation (project management)

    established and are tasks & authorities specified for the

    team leader and team members?

    nb

    2.2* Are the resources required for the project developmentplanned and available and are all changes displayed? nb

    2.3 Is there a project plan and has this been agreed with the

    customer?nb

    2.4 Is change management in the project ensured by the

    project organisation?nb

    2.5* Are the responsible personnel within the organisation

    and in the customer's company involved in the change

    control s stem?

    nb

    2.6 Is there a QM plan for the project? Is this implementedand monitored regularly for compliance? nb

    2.7* Is there an established escalation process and is this

    implemented effectively?nb

    P 3 Planning Product/Process Development

    Product

    3.1 Are the product-specific requirements laid down? nb

    3.2* Has manufacturing feasibility been assessed in a cross-

    functional manner, based on the requirements which

    have been determined for product & process?nb

    Questionaire VDA 6.3-2010

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    Questionaire VDA 6.3-2010

    P 4 Carrying out Product/Process Development

    Product

    4.1 Have the Product FMEA / Process FMEA been drawn

    up? Are they up-dated as the project progresses and are

    corrective actions laid down?nb

    4.2 Are the stipulations arising from the plans for product

    and process development put into effect? nb

    4.3 Are the personnel resources in place and qualified?nb

    4.4 Is the infrastructure in place and appropriate? nb

    4.5* Based on the requirements, are the necessary evidence

    and releases available for the various phases? nb

    4.8 Are the planning activities associated with sourcingoutside products and services implemented effectively? nb

    4.9 Is the transfer of the project to production controlled in

    order to secure the product launch?nb

    Process

    4.1 Have the Product FMEA / Process FMEA been drawn

    up? Are they up-dated as the project progresses and are

    corrective actions laid down?nb

    4.2 Are the stipulations arising from the plans for product

    and process development put into effect? nb

    4.3 Are the personnel resources in place and qualified?nb

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    Questionaire VDA 6.3-2010

    5.2 Are the customer's requirements taken into account in

    the supply chain?nb

    5.3 Have target agreements for delivery performance been

    agreed with suppliers and put into operation? nb

    5.4* Are the necessary approvals/releases available for the

    out-sourced products and services? nb

    5.5* Is the quality of the out-sourced products and services

    ensured?nb

    5.6 Are incoming goods stored appropriately? nb

    5.7 Are personnel qualified for the various tasks and are

    responsibilities defined?nb

    P 6 Process Analysis Serial Production

    Process step 1: Process Name 1

    1 Process Input

    6.1.1* Has the project been transferred from development to

    serial production?nb

    6.1.2 Are the necessary quantities / production batch sizes of

    incoming materials available at the right time and at the

    right place (stores; work-station)?nb

    6.1.3 Are incoming materials stored appropriately and aretransport facilities / packing arrangements suitable for

    the special characteristics of the incoming materials?nb

    6.1.4 Are the necessary identifications / records / approvals

    available and allocated appropriately to the incoming nb

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    QuestionPionts Comments / Assesment Remarks

    Questionaire VDA 6.3-2010

    6.3.2* Are the operators able to carry out their allotted tasks

    and are their qualifications kept up-to-date? nb

    6.3.3 Is there a personnel employment plan? nb

    4 Material Ressources

    6.4.1 How are the maintenance and overhaul of productionfacilities / tools controlled?

    nb

    6.4.2* Can the quality requirements be monitored effectively

    with the test, inspection and measurement facilities

    employed?

    nb

    6.4.3 Are the work-stations and test/inspection areas suitable

    for requirements?nb

    6.4.4 Are tools, equipment and test/inspection facilities

    stored correctly?nb

    5 Process Effectiveness Level

    6.5.1 Are target requirements set for product and process?nb

    6.5.2 Are quality and process data logged in such a way that

    they can be assessed?nb

    6.5.3* In the case of deviations from product and process

    requirements, are the causes analysed and the

    corrective actions checked for effectiveness?nb

    6.5.4* Are processes and products audited regularly? nb

    6 Process Result / Output

    6.6.1* Are the customer's requirements met in terms of

    product and process?nb

    6.6.2 Are quantities / production batch sizes aligned with

    requirements and are they forwarded to the next nb

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    6.1.4 Are the necessary identifications / records / approvals

    available and allocated appropriately to the incoming

    materials?

    nb

    6.1.5 Are changes to the product or process in the course of

    serial production tracked and documented? nb

    2 Work Content / Process Sequences6.2.1* Are all the relevant details listed in the production and

    test/inspection documents, based on the production

    control lan?

    nb

    6.2.2 Are production operations checked / approved and are

    setting data logged?nb

    6.2.3* Can the customer's specific product requirements be

    satisfied with the production facilities used?nb

    6.2.4* Are significant characteristics controlled in production?nb

    6.2.5 Are scrap, rework and setting parts kept separate and

    identified?nb

    6.2.6 Is the flow of materials and parts secured against mixing

    / wrong items?nb

    3 Personnel Support

    6.3.1 Are operators given responsibility and authority to

    monitor the quality of product and process?nb

    6.3.2* Are the operators able to carry out their allotted tasks

    and are their qualifications kept up-to-date? nb

    6.3.3 Is there a personnel employment plan? nb

    4 Material Ressources

    6.4.1 How are the maintenance and overhaul of production

    /nb

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    Questionaire VDA 6.3-2010

    6.6.2 Are quantities / production batch sizes aligned with

    requirements and are they forwarded to the next

    process stage in a targeted manner?

    nb

    6.6.3 Are products / components stored in an appropriate

    manner and are transport facilities / packing

    arrangements suitable for the special characteristics of

    the products / components?

    nb

    6.6.4 Are the necessary records / releases carried out and

    stored appropriately?nb

    Process step 3: Process Name 3

    1 Process Input

    6.1.1* Has the project been transferred from development to

    serial production?nb

    6.1.2 Are the necessary quantities / production batch sizes of

    incoming materials available at the right time and at the

    right place (stores; work-station)?nb

    6.1.3 Are incoming materials stored appropriately and are

    transport facilities / packing arrangements suitable for

    the special characteristics of the incoming materials?nb

    6.1.4 Are the necessary identifications / records / approvals

    available and allocated appropriately to the incomingmaterials? nb

    6.1.5 Are changes to the product or process in the course of

    serial production tracked and documented? nb

    2 Work Content / Process Sequences

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    Questionaire VDA 6.3-2010

    6.4.1 How are the maintenance and overhaul of production

    facilities / tools controlled?nb

    6.4.2* Can the quality requirements be monitored effectively

    with the test, inspection and measurement facilities

    employed?

    nb

    6.4.3 Are the work-stations and test/inspection areas suitable

    for requirements?

    nb

    6.4.4 Are tools, equipment and test/inspection facilities

    stored correctly?nb

    5 Process Effectiveness Level

    6.5.1 Are target requirements set for product and process?nb

    6.5.2 Are quality and process data logged in such a way that

    they can be assessed?nb

    6.5.3* In the case of deviations from product and process

    requirements, are the causes analysed and thecorrective actions checked for effectiveness? nb

    6.5.4* Are processes and products audited regularly? nb

    6 Process Result / Output

    6.6.1* Are the customer's requirements met in terms of

    product and process?nb

    6.6.2 Are quantities / production batch sizes aligned with

    requirements and are they forwarded to the next

    process stage in a targeted manner?

    nb

    6.6.3 Are products / components stored in an appropriate

    manner and are transport facilities / packing

    arrangements suitable for the special characteristics of

    the products / components?

    nb

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    QuestionPionts Comments / Assesment Remarks

    Questionaire VDA 6.3-2010

    2 Work Content / Process Sequences

    6.2.1* Are all the relevant details listed in the production and

    test/inspection documents, based on the production

    control lan?

    nb

    6.2.2 Are production operations checked / approved and are

    setting data logged?nb

    6.2.3* Can the customer's specific product requirements be

    satisfied with the production facilities used?nb

    6.2.4* Are significant characteristics controlled in production?nb

    6.2.5 Are scrap, rework and setting parts kept separate and

    identified?nb

    6.2.6 Is the flow of materials and parts secured against mixing

    / wrong items?nb

    3 Personnel Support

    6.3.1 Are operators given responsibility and authority tomonitor the quality of product and process?

    nb

    6.3.2* Are the operators able to carry out their allotted tasks

    and are their qualifications kept up-to-date? nb

    6.3.3 Is there a personnel employment plan? nb

    4 Material Ressources

    6.4.1 How are the maintenance and overhaul of production

    facilities / tools controlled?nb

    6.4.2* Can the quality requirements be monitored effectively

    with the test, inspection and measurement facilities

    em lo ed?

    nb

    6.4.3 Are the work-stations and test/inspection areas suitable

    for requirements?nb

    6 4 4 A l i d /i i f ili i

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    Questionaire VDA 6.3-2010

    6.6.3 Are products / components stored in an appropriate

    manner and are transport facilities / packing

    arrangements suitable for the special characteristics of

    the products / components?

    nb

    6.6.4 Are the necessary records / releases carried out and

    stored appropriately?

    nb

    Process step 5: Process Name 5

    1 Process Input

    6.1.1* Has the project been transferred from development to

    serial production?nb

    6.1.2 Are the necessary quantities / production batch sizes of

    incoming materials available at the right time and at the

    right place (stores; work-station)?nb

    6.1.3 Are incoming materials stored appropriately and are

    transport facilities / packing arrangements suitable for

    the special characteristics of the incoming materials?nb

    6.1.4 Are the necessary identifications / records / approvals

    available and allocated appropriately to the incoming

    materials?

    nb

    6.1.5 Are changes to the product or process in the course of

    serial production tracked and documented?nb

    2 Work Content / Process Sequences

    6.2.1* Are all the relevant details listed in the production and

    test/inspection documents, based on the production

    control plan?

    nb

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    Questionaire VDA 6.3-2010

    6.4.2* Can the quality requirements be monitored effectively

    with the test, inspection and measurement facilities

    employed?

    nb

    6.4.3 Are the work-stations and test/inspection areas suitable

    for requirements?nb

    6.4.4 Are tools, equipment and test/inspection facilities

    stored correctly?

    nb

    5 Process Effectiveness Level

    6.5.1 Are target requirements set for product and process?nb

    6.5.2 Are quality and process data logged in such a way that

    they can be assessed?nb

    6.5.3* In the case of deviations from product and process

    requirements, are the causes analysed and the

    corrective actions checked for effectiveness?nb

    6.5.4* Are processes and products audited regularly? nb

    6 Process Result / Output

    6.6.1* Are the customer's requirements met in terms of

    product and process?nb

    6.6.2 Are quantities / production batch sizes aligned with

    requirements and are they forwarded to the next

    rocess sta e in a tar eted manner?

    nb

    6.6.3 Are products / components stored in an appropriate

    manner and are transport facilities / packingarrangements suitable for the special characteristics of

    the products / components?

    nb

    6.6.4 Are the necessary records / releases carried out and

    stored appropriately?nb

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    QuestionPionts Comments / Assesment Remarks

    Questionaire VDA 6.3-2010

    6.2.1* Are all the relevant details listed in the production and

    test/inspection documents, based on the production

    control plan?

    nb

    6.2.2 Are production operations checked / approved and are

    setting data logged?nb

    6.2.3* Can the customer's specific product requirements be

    satisfied with the production facilities used?

    nb

    6.2.4* Are significant characteristics controlled in production?nb

    6.2.5 Are scrap, rework and setting parts kept separate and

    identified?nb

    6.2.6 Is the flow of materials and parts secured against mixing

    / wrong items?nb

    3 Personnel Support

    6.3.1 Are operators given responsibility and authority to

    monitor the quality of product and process?nb

    6.3.2* Are the operators able to carry out their allotted tasks

    and are their qualifications kept up-to-date? nb

    6.3.3 Is there a personnel employment plan? nb

    4 Material Ressources

    6.4.1 How are the maintenance and overhaul of production

    facilities / tools controlled?nb

    6.4.2* Can the quality requirements be monitored effectively

    with the test, inspection and measurement facilitiesem lo ed?

    nb

    6.4.3 Are the work-stations and test/inspection areas suitable

    for requirements?nb

    6.4.4 Are tools, equipment and test/inspection facilities

    stored correctly?nb

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    Questionaire VDA 6.3-2010

    6.6.4 Are the necessary records / releases carried out and

    stored appropriately?nb

    Process step 7: Process Name 7

    1 Process Input

    6.1.1* Has the project been transferred from development toserial production?

    nb

    6.1.2 Are the necessary quantities / production batch sizes of

    incoming materials available at the right time and at the

    right place (stores; work-station)?nb

    6.1.3 Are incoming materials stored appropriately and are

    transport facilities / packing arrangements suitable for

    the special characteristics of the incoming materials?nb

    6.1.4 Are the necessary identifications / records / approvals

    available and allocated appropriately to the incoming

    materials?

    nb

    6.1.5 Are changes to the product or process in the course of

    serial production tracked and documented? nb

    2 Work Content / Process Sequences

    6.2.1* Are all the relevant details listed in the production and

    test/inspection documents, based on the production

    control lan?

    nb

    6.2.2 Are production operations checked / approved and are

    setting data logged?nb

    6.2.3* Can the customer's specific product requirements be

    satisfied with the production facilities used?nb

    6 2 4* A i ifi h i i ll d i d i ?

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    Questionaire VDA 6.3-2010

    6.4.4 Are tools, equipment and test/inspection facilities

    stored correctly?nb

    5 Process Effectiveness Level

    6.5.1 Are target requirements set for product and process?nb

    6.5.2 Are quality and process data logged in such a way that

    they can be assessed? nb6.5.3* In the case of deviations from product and process

    requirements, are the causes analysed and the

    corrective actions checked for effectiveness?nb

    6.5.4* Are processes and products audited regularly? nb

    6 Process Result / Output

    6.6.1* Are the customer's requirements met in terms of

    product and process?nb

    6.6.2 Are quantities / production batch sizes aligned with

    requirements and are they forwarded to the next

    rocess sta e in a tar eted manner?

    nb

    6.6.3 Are products / components stored in an appropriate

    manner and are transport facilities / packing

    arrangements suitable for the special characteristics of

    the products / components?

    nb

    6.6.4 Are the necessary records / releases carried out and

    stored appropriately?

    nb

    Process step 8: Process Name 8

    1 Process Input

    6 1 1* H th j t b t f d f d l t t

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    Questionaire VDA 6.3-2010

    6.2.3* Can the customer's specific product requirements be

    satisfied with the production facilities used?nb

    6.2.4* Are significant characteristics controlled in production?nb

    6.2.5 Are scrap, rework and setting parts kept separate and

    identified?nb

    6.2.6 Is the flow of materials and parts secured against mixing/ wrong items? nb

    3 Personnel Support

    6.3.1 Are operators given responsibility and authority to

    monitor the quality of product and process?nb

    6.3.2* Are the operators able to carry out their allotted tasks

    and are their qualifications kept up-to-date? nb

    6.3.3 Is there a personnel employment plan? nb

    4 Material Ressources6.4.1 How are the maintenance and overhaul of production

    facilities / tools controlled?nb

    6.4.2* Can the quality requirements be monitored effectively

    with the test, inspection and measurement facilities

    em lo ed?

    nb

    6.4.3 Are the work-stations and test/inspection areas suitable

    for requirements?nb

    6.4.4 Are tools, equipment and test/inspection facilities

    stored correctly?

    nb

    5 Process Effectiveness Level

    6.5.1 Are target requirements set for product and process?nb

    6.5.2 Are quality and process data logged in such a way thatnb

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    Questionaire VDA 6.3-2010

    1 Process Input

    6.1.1* Has the project been transferred from development to

    serial production?nb

    6.1.2 Are the necessary quantities / production batch sizes of

    incoming materials available at the right time and at the

    right place (stores; work-station)?nb

    6.1.3 Are incoming materials stored appropriately and are

    transport facilities / packing arrangements suitable for

    the special characteristics of the incoming materials?nb

    6.1.4 Are the necessary identifications / records / approvals

    available and allocated appropriately to the incoming

    materials?

    nb

    6.1.5 Are changes to the product or process in the course of

    serial production tracked and documented? nb

    2 Work Content / Process Sequences

    6.2.1* Are all the relevant details listed in the production and

    test/inspection documents, based on the production

    control plan?

    nb

    6.2.2 Are production operations checked / approved and are

    setting data logged?nb

    6.2.3* Can the customer's specific product requirements be

    satisfied with the production facilities used?nb

    6.2.4* Are significant characteristics controlled in production? nb

    6.2.5 Are scrap, rework and setting parts kept separate and

    identified?nb

    6.2.6 Is the flow of materials and parts secured against mixingnb

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    Questionaire VDA 6.3-2010

    6.5.2 Are quality and process data logged in such a way that

    they can be assessed?nb

    6.5.3* In the case of deviations from product and process

    requirements, are the causes analysed and the

    corrective actions checked for effectiveness?nb

    6.5.4* Are processes and products audited regularly? nb6 Process Result / Output

    6.6.1* Are the customer's requirements met in terms of

    product and process?nb

    6.6.2 Are quantities / production batch sizes aligned with

    requirements and are they forwarded to the next

    process stage in a targeted manner?

    nb

    6.6.3 Are products / components stored in an appropriate

    manner and are transport facilities / packing

    arrangements suitable for the special characteristics ofthe products / components?

    nb

    6.6.4 Are the necessary records / releases carried out and

    stored appropriately?nb

    Process step 10: Process Name 10

    1 Process Input

    6.1.1* Has the project been transferred from development to

    serial production? nb6.1.2 Are the necessary quantities / production batch sizes of

    incoming materials available at the right time and at the

    right place (stores; work-station)?nb

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    Questionaire VDA 6.3-2010

    6.2.6 Is the flow of materials and parts secured against mixing

    / wrong items?nb

    3 Personnel Support

    6.3.1 Are operators given responsibility and authority to

    monitor the quality of product and process?nb

    6.3.2* Are the operators able to carry out their allotted tasks

    and are their qualifications kept up-to-date? nb

    6.3.3 Is there a personnel employment plan? nb

    4 Material Ressources

    6.4.1 How are the maintenance and overhaul of production

    facilities / tools controlled?nb

    6.4.2* Can the quality requirements be monitored effectively

    with the test, inspection and measurement facilities

    em lo ed?

    nb

    6.4.3 Are the work-stations and test/inspection areas suitable

    for requirements?nb

    6.4.4 Are tools, equipment and test/inspection facilities

    stored correctly?nb

    5 Process Effectiveness Level

    6.5.1 Are target requirements set for product and process?nb

    6.5.2 Are quality and process data logged in such a way that

    they can be assessed?nb

    6.5.3* In the case of deviations from product and processrequirements, are the causes analysed and the

    corrective actions checked for effectiveness?nb

    6.5.4* Are processes and products audited regularly? nb

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    Questionaire VDA 6.3-2010

    7.4 If there are deviations from quality requirements, are

    failure analyses carried out and corrective actions

    implemented effectively?nb

    7.5 Is there a process which ensures that analysis of

    defective parts is carried out?nb

    7.6Are personnel qualified for the various tasks and are

    responsibilities defined? nb

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    Improvement Program VDA 6.3-2010 Date:Supplier: Client:

    To be filled by auditor to be filled by audited party

    A Development

    P 2 Project Management

    2.1 nb

    2.2* nb

    2.3 nb

    2.4 nb

    2.5* nb

    2.6 nb

    2.7* nb

    P 3 Planning Product/Process Development

    Product

    3.1 nb

    3.2* nb

    3.3 nb

    3.4 nb

    3.5 nb

    Process

    3.1 nb

    3.2* nb

    3.3 nb

    3.4 nb

    3.5 nb

    P 4 Carrying out Product/Process Development

    Product

    TimingRespon-

    sibles

    EffectivenessPos. Quest

    No.

    Weaknesses, recommended actions,

    findings

    PointsActions and cause analysis by the

    organisation

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    TimingRespon-

    siblesEffectiveness

    Pos. Quest

    No.

    Weaknesses, recommended actions,

    findingsPoints

    Actions and cause analysis by the

    organisation

    4.1 nb

    4.2 nb

    4.3 nb

    4.4 nb

    4.5* nb

    4.8 nb

    4.9 nb

    Process

    4.1 nb

    4.2 nb

    4.3 nb

    4.4 nb

    4.5* nb

    4.6 nb

    4.7 nb

    4.8 nb

    4.9 nb

    B Full Production

    P 5 Supplier Management

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    TimingRespon-

    siblesEffectiveness

    Pos. Quest

    No.

    Weaknesses, recommended actions,

    findingsPoints

    Actions and cause analysis by the

    organisation

    5.1* nb

    5.2 nb

    5.3 nb

    5.4* nb

    5.5* nb

    5.6 nb

    5.7 nb

    P 6 Process Analysis Serial Production

    Process step 1: Process Name 1

    1 Process Input

    6.1.1* nb

    6.1.2 nb

    6.1.3 nb

    6.1.4 nb

    6.1.5 nb

    2 Work Content / Process Sequences

    6.2.1* nb

    6.2.2 nb

    6.2.3* nb

    6.2.4* nb

    6.2.5 nb

    6.2.6 nb

    3 Personnel Support

    6.3.1 nb

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    TimingRespon-

    siblesEffectiveness

    Pos. Quest

    No.

    Weaknesses, recommended actions,

    findingsPoints

    Actions and cause analysis by the

    organisation

    6.3.2* nb

    6.3.3 nb

    4 Material Ressources6.4.1 nb

    6.4.2* nb

    6.4.3 nb

    6.4.4 nb

    5 Process Effectiveness Level

    6.5.1 nb

    6.5.2 nb

    6.5.3* nb

    6.5.4* nb

    6 Process Result / Output

    6.6.1* nb

    6.6.2 nb

    6.6.3 nb

    6.6.4 nb

    Process step 2: Process Name 2

    1 Process Input6.1.1* nb

    6.1.2 nb

    6.1.3 nb

    6.1.4 nb

    6.1.5 nb

    2 Work Content / Process Sequences

    6.2.1* nb

    6.2.2 nb6.2.3* nb

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    TimingRespon-

    siblesEffectiveness

    Pos. Quest

    No.

    Weaknesses, recommended actions,

    findingsPoints

    Actions and cause analysis by the

    organisation

    6.2.4* nb

    6.2.5 nb

    6.2.6 nb

    3 Personnel Support

    6.3.1 nb

    6.3.2* nb

    6.3.3 nb

    4 Material Ressources

    6.4.1 nb

    6.4.2* nb

    6.4.3 nb

    6.4.4 nb

    5 Process Effectiveness Level

    6.5.1 nb

    6.5.2 nb

    6.5.3* nb

    6.5.4* nb

    6 Process Result / Output

    6.6.1* nb

    6.6.2 nb

    6.6.3 nb

    6.6.4 nb

    Process step 3: Process Name 3

    1 Process Input

    6.1.1* nb

    6.1.2 nb

    6.1.3 nb

    6.1.4 nb

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    TimingRespon-

    siblesEffectiveness

    Pos. Quest

    No.

    Weaknesses, recommended actions,

    findingsPoints

    Actions and cause analysis by the

    organisation

    6.1.5 nb

    2 Work Content / Process Sequences

    6.2.1* nb6.2.2 nb

    6.2.3* nb

    6.2.4* nb

    6.2.5 nb

    6.2.6 nb

    3 Personnel Support

    6.3.1 nb

    6.3.2* nb

    6.3.3 nb

    4 Material Ressources

    6.4.1 nb

    6.4.2* nb

    6.4.3 nb

    6.4.4 nb

    5 Process Effectiveness Level

    6.5.1 nb

    6.5.2 nb

    6.5.3* nb

    6.5.4* nb

    6 Process Result / Output

    6.6.1* nb

    6.6.2 nb

    6.6.3 nb

    6.6.4 nb

    Process step 4: Process Name 4

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    TimingRespon-

    siblesEffectiveness

    Pos. Quest

    No.

    Weaknesses, recommended actions,

    findingsPoints

    Actions and cause analysis by the

    organisation

    1 Process Input

    6.1.1* nb

    6.1.2 nb6.1.3 nb

    6.1.4 nb

    6.1.5 nb

    2 Work Content / Process Sequences

    6.2.1* nb

    6.2.2 nb

    6.2.3* nb

    6.2.4* nb

    6.2.5 nb

    6.2.6 nb

    3 Personnel Support

    6.3.1 nb

    6.3.2* nb

    6.3.3 nb

    4 Material Ressources

    6.4.1 nb

    6.4.2* nb

    6.4.3 nb

    6.4.4 nb

    5 Process Effectiveness Level

    6.5.1 nb

    6.5.2 nb

    6.5.3* nb

    6.5.4* nb

    6 Process Result / Output6.6.1* nb

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    Pos. Quest

    No.

    Weaknesses, recommended actions,

    findingsPoints

    Actions and cause analysis by the

    organisation

    6.6.2 nb

    6.6.3 nb

    6.6.4 nb

    Process step 5: Process Name 5

    1 Process Input

    6.1.1* nb

    6.1.2 nb

    6.1.3 nb

    6.1.4 nb

    6.1.5 nb

    2 Work Content / Process Sequences

    6.2.1* nb

    6.2.2 nb

    6.2.3* nb

    6.2.4* nb

    6.2.5 nb

    6.2.6 nb

    3 Personnel Support

    6.3.1 nb

    6.3.2* nb

    6.3.3 nb

    4 Material Ressources

    6.4.1 nb

    6.4.2* nb

    6.4.3 nb

    6.4.4 nb

    5 Process Effectiveness Level6.5.1 nb

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    Pos. Quest

    No.

    Weaknesses, recommended actions,

    findingsPoints

    Actions and cause analysis by the

    organisation

    6.5.2 nb

    6.5.3* nb

    y 6.5.4* nb

    6 Process Result / Output

    6.6.1* nb

    6.6.2 nb

    6.6.3 nb

    6.6.4 nb

    Process step 6: Process Name 6

    1 Process Input

    6.1.1* nb

    6.1.2 nb

    6.1.3 nb

    6.1.4 nb

    6.1.5 nb

    2 Work Content / Process Sequences

    6.2.1* nb

    6.2.2 nb

    6.2.3* nb

    6.2.4* nb

    6.2.5 nb

    6.2.6 nb

    3 Personnel Support

    6.3.1 nb

    6.3.2* nb

    6.3.3 nb

    4 Material Ressources6.4.1 nb

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    Pos. Quest

    No.

    Weaknesses, recommended actions,

    findingsPoints

    Actions and cause analysis by the

    organisation

    6.4.2* nb

    6.4.3 nb

    6.4.4 nb

    5 Process Effectiveness Level

    6.5.1 nb

    6.5.2 nb

    6.5.3* nb

    6.5.4* nb

    6 Process Result / Output

    6.6.1* nb

    6.6.2 nb

    6.6.3 nb

    6.6.4 nb

    Process step 7: Process Name 7

    1 Process Input

    6.1.1* nb

    6.1.2 nb

    6.1.3 nb

    6.1.4 nb

    6.1.5 nb

    2 Work Content / Process Sequences

    6.2.1* nb

    6.2.2 nb

    6.2.3* nb

    6.2.4* nb

    6.2.5 nb

    6.2.6 nb3 Personnel Support

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    Pos. Quest

    No.

    Weaknesses, recommended actions,

    findingsPoints

    Actions and cause analysis by the

    organisation

    6.3.1 nb

    6.3.2* nb

    6.3.3 nb4 Material Ressources

    6.4.1 nb

    6.4.2* nb

    6.4.3 nb

    6.4.4 nb

    5 Process Effectiveness Level

    6.5.1 nb

    6.5.2 nb

    6.5.3* nb

    6.5.4* nb

    6 Process Result / Output

    6.6.1* nb

    6.6.2 nb

    6.6.3 nb

    6.6.4 nb

    Process step 8: Process Name 81 Process Input

    6.1.1* nb

    6.1.2 nb

    6.1.3 nb

    6.1.4 nb

    6.1.5 nb

    2 Work Content / Process Sequences

    6.2.1* nb

    6.2.2 nb

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    Pos. Quest

    No.

    Weaknesses, recommended actions,

    findingsPoints

    Actions and cause analysis by the

    organisation

    6.2.3* nb

    6.2.4* nb

    6.2.5 nb

    6.2.6 nb

    3 Personnel Support

    6.3.1 nb

    6.3.2* nb

    6.3.3 nb

    4 Material Ressources

    6.4.1 nb

    6.4.2* nb

    6.4.3 nb

    6.4.4 nb

    5 Process Effectiveness Level

    6.5.1 nb

    6.5.2 nb

    6.5.3* nb

    6.5.4* nb

    6 Process Result / Output

    6.6.1* nb

    6.6.2 nb

    6.6.3 nb

    6.6.4 nb

    Process step 9: Process Name 9

    1 Process Input

    6.1.1* nb

    6.1.2 nb

    6.1.3 nb

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    Weaknesses, recommended actions,

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    Actions and cause analysis by the

    organisation

    6.1.4 nb

    6.1.5 nb

    2 Work Content / Process Sequences6.2.1* nb

    6.2.2 nb

    6.2.3* nb

    6.2.4* nb

    6.2.5 nb

    6.2.6 nb

    3 Personnel Support

    6.3.1 nb

    6.3.2* nb

    6.3.3 nb

    4 Material Ressources

    6.4.1 nb

    6.4.2* nb

    6.4.3 nb

    6.4.4 nb

    5 Process Effectiveness Level

    6.5.1 nb

    6.5.2 nb

    6.5.3* nb

    6.5.4* nb

    6 Process Result / Output

    6.6.1* nb

    6.6.2 nb

    6.6.3 nb

    6.6.4 nb

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    Actions and cause analysis by the

    organisation

    Process step 10: Process Name 10

    1 Process Input

    6.1.1* nb

    6.1.2 nb

    6.1.3 nb

    6.1.4 nb

    6.1.5 nb

    2 Work Content / Process Sequences

    6.2.1* nb

    6.2.2 nb

    6.2.3* nb

    6.2.4* nb

    6.2.5 nb

    6.2.6 nb

    3 Personnel Support

    6.3.1 nb

    6.3.2* nb

    6.3.3 nb

    4 Material Ressources

    6.4.1 nb

    6.4.2* nb

    6.4.3 nb

    6.4.4 nb

    5 Process Effectiveness Level

    6.5.1 nb

    6.5.2 nb

    6.5.3* nb

    6.5.4* nb

    6 Process Result / Output

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