Volvo Supplier Quality Assurance Manualpdf
Volvo Supplier Quality Assurance Manualpdf
Volvo Supplier Quality Assurance Manualpdf
May 2016
SECTION 0.0
INTRODUCTION
The Quality Challenge
Every day at VOLVO, we are working to improve our organization, our processes and the skill of our
employees to be the best in class. We are committed to quality excellence, a customer-focused
process approach and continuous improvement. We expect and encourage our suppliers to adopt
these same principles and practices.
The mission of VOLVO Purchasing is to provide a competitive advantage to our organization and our
customers through the selection, development and partnership with suppliers that are capable of
exceptional performance. VOLVO is actively seeking to attract suppliers that are capable of delivering
superior products in terms of quality, delivery, price and features.
In support of our strategy, this manual describes the sourcing process used to identify and select
suppliers that share the VOLVO “Drive for Quality”. This manual also covers the expectations,
requirements, guidelines and practices expected of suppliers doing business with VOLVO.
Once selected, our goal is to work closely with these suppliers to develop a strong, stable, structured
relationship.
VOLVO products have always been characterised by quality and safety. Maintaining the reputation of
selling the highest quality and safest products in the market is a must for us. We expect suppliers to
contribute to maintaining this reputation by the care they invest in the parts they produce and deliver.
VOLVO suppliers are expected to extend the requirements in this manual to their suppliers and assume
responsibility to ensure that quality is consistent through their supply chain.
This document is intended to serve as a reference document and a guide to understanding VOLVO
specific requirements and the responsibility shared by our suppliers in ensuring products that meet
consistently high standards for quality and safety.
With your commitment to participate as a VOLVO supplier, we will succeed in our mission to our
customers and at the same time begin a long term and mutually beneficial relationship.
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SECTION 0.0
Table of Contents
INTRODUCTION…………………………………………………………..…… 2
TABLE OF CONTENTS………………………………………………..……… 3
USING THIS DOCUMENT……………………………………………..……… 4
BASIC REQUIREMENTS………………………………………………..….… 6
PERFORMANCE EXPECTATIONS………………………………… 7
MANAGEMENT SYSTEM REQUIREMENTS……………………… 8
SOURCING……………………………………………………………………........9
QUALITY MANAGEMENT SYSTEM REQUIREMENT…………… 10
SHORT SUPPLIER EVALUATION MODEL………………………… 10
CONFIDENTIALITY AGREEMENT…………………………………… 10
REQUEST FOR QUOTATION……………………………………..… 10
SUPPLIER EVALUATION MODEL…………………………………… 11
INDEX AUDITS………………………………………………………… 11
FINAL AGREEMENT……………………………………………………. 11
ADVANCED PRODUCT QUALITY PLANNING………………………..………12
SCOPE…………………………………………………………………… 13
APQP – PLANNING…………………………………………………… 13
RESPONSIBILITIES IN APQP………………………………………… 13
KEY COMPONENT DEFINITION………………………………………14
APQP REVIEWS………………………………………………………… 14
SOFTWARE APQP REQUIREMENTS……………………………… 15
PRODUCTION PART APPROVAL PROCESS…………………….....……….17
REFERENCE…………………………………………………………… 18
PROCESS……………………………………………………………… 18
SIGNIFICANT PRODUCTION RUN………………………………… 19
DOCUMENTATION REQUIREMENTS……………………………… 20
APPROVAL OR NEW OR REVISED SOFTWARE……………….. 21
VOLVO SPECIFIC REQUIREMENTS……………………………………..……23
VOLVO SPECIFIC REQUIREMENTS ……………………………… 24
REVIEW OF TECHNICAL SPECIFICATIONS……………………… 24
PRODUCT APPLICATION AGREEMENT…………………………… 25
PART HANDLING REVIEW…………………………………………… 25
SPECIAL CHARACTERISTICS…………………………………….… 26
LEGAL REQUIREMENTS - CONFORMITY OF PRODUCTION... 27
CLEANLINESS REQUIREMENTS…………………………………… 28
PROTOTYPE PARTS………………………………………………… 29
REACH COMPLIANCEAND IMDS REPORTING …………………. 31
PRE-LAUNCH CONTROL PLANS…………………………………... 31
AFTERMARKET PARTS REQUIREMENTS……………………….. 32
MAJOR SYSTEMS OR ORGANIZATION CHANGES……………. 32
SAFETY MANAGEMENT…………………………………………….…………..33
DEFINITION…………………………………………………………… 34
RESPONSIBILITY……………………………………………………… 34
IDENTIFICATION OF SAFETY CHARACTERISTICS……………… 34
PRODUCTION REQUIREMENTS………………………………….… 35
SAFETY MANAGEMENT AUDITS…………………………………… 36
LOT TRACEABILITY REQUIREMENTS……………………………… 36
PASS THROUGH PART REQUIREMENTS……………….………. 36
PRODUCTION REQUIREMENTS……………………………………………….38
PRODUCT PROCESS CHANGE NOTICE………………………… 39
REQUESTING DEVIATIONS…………………………………………. 40
LOT TRACEABILITY…………………………………………………… 40
FIRST IN FIRST OUT CONTROL…………………………………… 41
SUB-TIER SUPPLIER REQUIREMENTS……………..……….…… 41
PACKAGING……………………………………………….…………… 41
WARRANTY………………………………………………………….… 42
LABORATORY REQUIREMENTS…………………………………… 42
RECORD RETENTION…………………………………………………. 42
PERFORMANCE MEASUREMENT AND CORRECTIVE ACTION…………43
MANAGEING NONCONFORMING PARTS …………………….…. 44
SCORE CARD PRESENTATION …………………………………… 45
QUALITY PERFORMANCE MEASUREMENT …………..………… 46
THE VOLVO PROCESS AUDIT …………………………….………. 47
CONTINUOUS IMPROVEMENT ……………………………......….… 48
LOW PERFORMING SUPPLIER …………………………………… 48
FIELD QUALITY ISSUES…………………………………………….. 49
GLOSSARY………………………………………………………………...………51
REVISION RECORD…………………………………………………………...….52
Page 3 of 53
SECTION 0.0
0.3 Scope
This Supplier Quality Assurance Manual is a joint document recognized and used by the following
organizations: VOLVO Truck, Mack Trucks, Renault Trucks, VOLVO Bus, VOLVO Bus North America
(VBNA – which includes both Nova Bus and Prevost Bus), UD Trucks, Eicher, DFCV and Renault Trucks
Defense.
To simplify the text in this document, the name VOLVO refers to this collective group of companies.
VEHICLE refers to both trucks or busses.
Page 4 of 53
SECTION 0.0
single Super User at the parent level. Once a Super User is assigned for a supplier, that person will be
responsible for administering the access rights for their supplier code(s). Technical support will be offered
and available to assist super users if necessary.
Additional guidelines, communication kits, and templates are posted in the quality section of this E-library.
The latest version of this Supplier Quality Assurance Manual is available in the Quality Section within the E-
Library.
http://supplierportal.volvo.com/VSP/INT/EN/E-LIBRARY/Pages/elibrary.aspx
Page 5 of 53
BASIC REQUIREMENTS
Performance Expectations and
Management Requirements
RESULTS
Performance
Processes
For specific products, additional part specific targets may be defined in the Request for Quotation.
MEASUREMENT TARGET
Field Quality
• Warranty/Fault Frequency Zero Safety Issues
• External Campaign/Recall
• Quality Journal (QJ) ref Section 8.7
Zero Field Issues
• Customer Claims (for powertrain)
0 km Quality
• Internal Campaigns
• First Time Through (FTT) Zero production impact
• Line Stop QPM < 50
• Product Audit Zero PPM as per vision*
• QPM
• PPM
*Actual targets for a supplier may be modified based on commodity, product technology, function
or part criticality. Exceptions must be documented in a Long Term Agreement, or contract.
Page 7 of 53
SECTION 1.0
1.2 MANAGEMENT SYSTEMS REQUIREMENTS
Index Audit
Score over 60%
(Applies to suppliers of Index Score greater than 80%
No stopping parameters
related processes, Section 2.6)
Compliance to
Review of Technical Specification (RTS)
Conformity of Production (COP),
VOLVO Customer Specific
Part Application Agreement (PAA),
Requirements
Part Handling Review (PHR),
Conforming Parts Out Of Tool In Plant
Delivery (CPOT IPD)
SPICE level 3
Software
Current certificate or equivalent by an
(Software Suppliers)
accredited 3rd party
Ethics Corporate Social Responsibility
Key Element Procedure 6 Self-assessment Score over 60% Preferred 100%
Corporate Social Responsibility No stopping parameters
Materials Management Operations
Logistic evaluation
Guidelines/Logistics Evaluation
Key Element Procedure 7
(MMOG/LE) self-assessment level A
Logistic
(Optional for VBNA suppliers)
EDI
Key Element Procedure
100% Electronic communication
1 – General
7 - Logistic
Page 8 of 53
SECTION 2.0
SOURCING
Join the VOLVO Team
Quality
Request Sign
Management Short Confidentiality Index
for SEM Contracts, &
System SEM Agreement Audit
Quote Agreements
Requirements
The awarding of business to a supplier is one Suppliers have an important role to play in
of the most important decisions made by the selection process.
VOLVO Purchasing. It directly impacts our • Actively participating in evaluation
ability to deliver to their customers, remain audits performed by VOLVO.
competitive and deliver future developments • Demonstrating their capability to
through projects. achieve future quality results.
• Responding to action plans to reach
The VOLVO Global Sourcing Process is the requested level.
designed to ensure that all divisions of
VOLVO have the opportunity to contribute to The following chapter explains the main
the selection process and ensures the steps in the process required to become a
coordination of these decisions across all VOLVO supplier. In this section the
VOLVO locations. information that suppliers can expect to
receive and the evaluations that are
It’s the first step in building a strong required are further defined.
relationship between VOLVO and our
suppliers.
Page 9 of 53
SECTION 2.0
2.1 QUALITY MANAGEMENT SYSTEM REQUIREMENT
2.1.1 All potential suppliers must have a quality system compliant to ISO 9001 as a minimum. Suppliers to the
truck brands are required to have a Quality Management System meeting the requirements of ISO/TS 16949.
Suppliers are required to have an Environmental Management system compliant to ISO 14001 in place,
functioning and approved by a third party registrar.
2.2.2 Potential suppliers can access this site, complete the SSEM and submit it to VOLVO purchasing for
consideration. This site is a public site and does not require VOLVO granted access.
The short version of Supplier Evaluation 2.2.3 Typically the first formal contact with a supplier
Model provides a simple way for potential will be a Request for Information (RFI). At that time
suppliers to share their standards and suppliers may be requested to complete the Short
capabilities with VOLVO. Supplier Evaluation Model (SSEM).
2.2.4 This evaluation collects general data about the company, its products and capabilities. Specific quality
topics included in the SSEM are:
• Quality Systems: Application and certification by an accredited third party to ISO 9001 or ISO/TS
16949 Quality Management System and ISO-14001 Environmental Management System.
• Quality Performance: Past performance in quality, reliability and deliveries.
• Reliability: Practices in place for verification and validation testing that ensures their products will
meet the minimum useful life expectations.
• Corporate and social responsibility.
2.2.5 Current suppliers to VOLVO that have not participated in a recent evaluation may be requested to
complete a Short SEM or participate in a normal on-site SEM prior to the award of additional business.
VOLVO routinely monitors all current suppliers’ based on their performance as measured in the Supplier
Scorecard (PPM, QPM, recent audit scores, Inspection Reports, Low performing Supplier (LPS) status, etc.).
Based on these results, VOLVO may request a new SSEM be completed or request further evaluation
audits.
2.4.2 The quality requirements and targets are highlighted in the quality section of the RFQ. Suppliers are
expected to be able to fulfill all quality requirements. VOLVO may audit the evidence related to the
fulfillment of these quality requirements. In the event there are requirements that cannot be fulfilled,
suppliers may be required to develop and submit an action plan with the returned RFQ. Suppliers are
Page 10 of 53
SECTION 2.0
responsible for all costs associated with the fulfilment of the quality requirements. Some of these
requirements may require testing at Volvo approved testing facilities. These costs should be included in all
RFQ responses.
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SECTION 3.0
Key
APQP Software
Scope Planning Responsibilities Components
Reviews APQP
Staying competitive in the markets where In 2006, VOLVO adopted the AIAG guideline
VOLVO participates requires continuous for APQP as the standard planning method for
development of new products and regular suppliers bringing products to production.
improvements to existing product.
Suppliers are expected to develop a detailed
Supporting the introduction of new products Advanced Product Quality Plan for the
requires a well-defined and organized development and prove-out of processes used
process for project planning and launch. to produce VOLVO products.
VOLVO organizes all new product The following chapter describes the
introductions into projects. Suppliers are expectations related to APQP and
required to have an effective project planning requirements for synchronizing the plan with
process that is capable of supporting the the VOLVO Product Development Process
VOLVO process and timing for project (DVP).
management.
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SECTION 3.0
3.1 SCOPE
3.1.1 We believe that the ultimate quality of delivered
VOLVO requires suppliers to use Advanced parts is determined during the design and development
Product Quality Planning (APQP) as a tool phase of the production process.
to support process development,
integration and validation. The AIAG VOLVO expects suppliers to create product launch plans
publication “Advanced Product Quality to support:
Planning (APQP) and Control Plan” should
• Launch of all new components intended for serial
be used as a reference in developing these
production.
plans. Supplier’s plans should include
• Significant changes to existing products, or
VOLVO specific requirements.
process
• Development of new manufacturing processes
3.1.2 Recently VOLVO has made significant changes to the project development cycle. The major impact
of these changes is to front load the development activities of a project. To support this, new activities have
been added to the supplier requirements or additional emphasis added to existing activities of the project.
In this manual you will find the addition of Conforming Part Out of Tool/ In Plant Delivery requirements and
more emphasis on the “C” Build process. These additional requirements require attention from suppliers
supporting product development during a project.
APQP identifies the tasks to be 3.2.2 An example of a generic project plan, as expected
completed, the expected timing, by VOLVO, is available on the VOLVO supplier portal.
assigned responsibility for completion Suppliers are encouraged to develop a plan suited to
and the critical path. their specific business.
http://supplierportal.volvo.com/vsp/int/en/E-
Library/Quality/3P_and_Powertrain/APQP_PPAP/Pages/APQP_PPAP.aspx
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SECTION 3.0
3.4 KEY COMPONENTS DEFINITION
3.4.1 All parts used in the vehicle are important to customer satisfaction and the safe, reliable operation of
the final product. However, there are some parts that require additional attention. At the start of a project, a
cross-functional project team identifies parts that will be subjected to closer control and monitoring. These
parts are designated as Key Components. The VOLVO buyer will notify suppliers of parts selected as Key
Components and any associated requirements. Suppliers of Key Components will typically be expected to
participate in APQP and joint steering committee reviews during the project.
3.5.3 To support these reviews, VOLVO has developed a checklist designed to document the project status
at each review. The information related to the “APQP review” file is available on the supplier portal.
Suppliers are responsible to complete and maintain the information for each review meeting. The completed
form will be used by the joint team as the basis for evaluating the project status.
http://supplierportal.volvo.com/vsp/int/en/E-
Library/Quality/3P_and_Powertrain/APQP_PPAP/Pages/APQP_PPAP.aspx
3.5.4 The following illustration demonstrates the relationship between VOLVO’s Product Development
Process (DVP) and the supplier’s project plan.
Page 14 of 53
SECTION 3.0
3.6.2 There are six Joint Reviews in a normal software development project:
• SW APQP Kick Off
• Project Planning Review
• Requirements Review
• Initial Design Review
• Final Design Review
• (SW) PPAP Review
3.6.3 As the majority of software development occurs during the product design phase of the project, most of
the reviews occur during this phase. The only exception is the Software (SW) PPAP Review.
Page 15 of 53
SECTION 3.0
3.6.4 The requirements applicable to supplier software projects and quality assurance system are described
in a separate requirement document called Quality and Development Process Requirements
(QDPR). Supplier delivering software to VOLVO shall be certified to level 3 according to an ISO 15504
Software Process Improvement and Capability dEtermination (SPICE) assessment, or have a plan for
achieving certification according to the automotive SPICE assessment model( see
www.automotivespice.com).
3.6.5 . Software APQP reviews are optional for VBNA suppliers unless requested by the responsible VBNA
SQE. VBNA software suppliers are encouraged to use Advanced Product Quality Planning planning as a
project management tool.
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SECTION 4.0
PRODUCTION PART
APPROVAL PROCESS (PPAP)
Approval of New or Revised Parts
The Production Part Approval Process Sample parts and the supporting
(PPAP) demonstrates that the manufacturing documentation are submitted to show
process used to produce parts for VOLVO is evidence that:
fully developed, thoroughly tested, and • The design records and specifications
capable of serial production of parts have been properly understood and met
conforming to the technical specifications. • The manufacturing process has the
capability to produce conforming parts in
For the PPAP (as for the APQP) VOLVO the actual production environment.
follows the AIAG requirements, using the • The manufacturing process has the
requirements applicable for trucks and heavy capacity to support production quantities
equipment. at a consistent quality level.
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SECTION 4.0
4.1 REFERENCE
4.1.1 Suppliers shall ensure that the PPAP document and sample submissions are in accordance
with the requirements of the Automotive Industry Action Group (AIAG) PPAP Manual (latest
edition, using requirement as applied to truck and heavy equipment). Suppliers of Aftermarket Parts
shall follow the AIAG requirements document Service Production Part Approval Process (Service PPAP)
First Edition June 2014. Additional guidelines and a copy of the Part Submission Warrant (PSW)
template are available on the VOLVO supplier portal. This requirement is also valid for the Software
specific Submission Warranty(SSW)".
4.1.2 VOLVO requires its suppliers to follow the Customer Notification and Submission requirements as
specified in the AIAG PPAP Manual. This includes but is not limited to:
VOLVO REQUIRES PPAP APPROVAL PRIOR TO SHIPMENT OF ANY PRODUCTS FOR USE IN
CUSTOMER VEHICLES
4.2 PROCESS
4.2.1 VOLVO uses a four step release process for new part development. These releases are labelled,
“A”, “B”, “C” and “P” releases, with the “P” release being the final approved document package for the
start of production. The PPAP process can only be completed and approved based on the final or “P”
release of the specifications.
4.2.2 The PPAP Sample Order: When the design has reached the “C” release stage, the VOLVO Buyer
will issue a Sample Order to notify the supplier that a PPAP is required. At this point, the design is
considered firm enough that suppliers are authorized to place tooling orders and start the production
process design and development. Suppliers are responsible to verify that all technical documentation
(Part Version Report, Drawing, Technical Requirements etc…) has been supplied. Any questions
regarding the technical document package should be directed to the host buyer. This early release is
intended to give suppliers as much time and information as possible to prepare for start of production.
This sample order will be amended once the “P” documents and specifications are completed.
4.2.3 PPAPs can only be approved based on the “P” release of the drawing and document package,
unless there is a clear agreement with the VOLVO Supplier Quality Engineer (SQE) and an approved
deviation.
4.2.4 The preliminary target date for PPAP submission may be included as part of the RFQ information.
Additional information concerning the target date for PPAP submission will be included in the Sample
Order. PPAP submission dates must be planned as a milestone in the supplier’s APQP plan. Any
issues, delays or changes to the PPAP target date should be communicated to the VOLVO buyer and
SQE.
Page 18 of 53
SECTION 4.0
* For suppliers delivering small production runs, the requirement for Cpk studies and Significant
Production Run may be waived with approval by the SQE.
* Cpk studies and Significant production Runs are waived for Service Part suppliers
4.2.6 Upon satisfactory completion of all required measurements and tests, the supplier shall complete the
required information on the Part Submission Warrant (PSW) and/or the Software Submission
Completing the PSW
• Suppliers are requested to use the VOLVO PSW form that is available on the supplier portal.
• A separate PSW shall be completed for each VOLVO part number unless otherwise
specified by the SQE.
• The PSW/SSW shall be signed by the authorized supplier representative before
submission.
4.2.7 VOLVO SQE will review all PPAP packages and assign one of the following:
• Fully approved and in compliance with all specifications.
• Conditional or Interim Approval.
• Not approved.
4.2.8 In the case where interim approval is given, it must be supported with an approved Deviation. All
deviation requests require review and approval by both VOLVO Product Development and the SQE. Full
approval of the deviation also requires a plan from the supplier that addresses correction of all open issues.
Suppliers may request a deviation using the Global Deviation Request. The completed form is submitted by
email to the responsible SQE, buyer or to the email location indicated on the deviation form. The form is
available on the VOLVO Supplier Portal in the Serial Production section of the Quality E-Library or by
accessing the link:
http://supplierportal.volvo.com/vsp/int/en/E-
Library/Quality/3P_and_Powertrain/serial_production/Pages/Serialproduction.aspx
4.3.2. The “Significant Production Run” requires that an adequate quantity of parts be produced to allow:
• Overall process stabilization
• Accurate calculation of manufacturing cycle time
• Determine production through-put time
• Capacity assessments
• Completion of capability studies
4.3.3. The minimum quantity of parts to be produced during the Significant Production Run is specified by
VOLVO but can be increased by the supplier. The number of parts produced during the Significant
Production Run should be determined by the type of equipment, tooling and production processes required
by the type of part. Suppliers should ensure enough parts are produced during the Significant Production
Run to ensure that the process is fully tested. Samples used for the PPAP must be taken from the parts
produced during the run.
4.3.4 The SPR also provides a good opportunity to identify and correct potential manufacturing process
bottlenecks. To be fully accurate, the capacity calculated from the SPR results should take into account the
actual OEE results from the process and include any planned down time.
THE PPAP MUST BE FULLY APPROVED OR HAVE INTERIM PPAP APPROVAL WITH
DOCUMENTATION REQUIREMENTS-LEVEL
APPROVED DEVIATION BEFORE STARTING OF SUBMISSION
SERIAL PRODUCTION
Page 19 of 53
SECTION 4.0
4.4 DOCUMENTATION REQUIREMENTS
4.4.1 Suppliers are required to submit a Level 4 PPAP package for all components unless other
arrangements have been agreed between VOLVO and the supplier.
4.4.2 Suppliers shall only submit PPAP packages based on the production-released drawings (P-
Drawings). A copy of the VOLVO drawing, the controlling Part Version Report PVR (Ref. 5.1.3) and
the Technical Specification (if applicable) must be included in the submission package. Suppliers
are required to submit the current revision of the VOLVO drawings, Part Version Report, and
Technical Requirements to ensure that the Production Part Approval has been conducted on the
correct revision of the specifications. PPAPs cannot be approved based on supplier’s drawings.
Balloons supporting dimensional checks must be done on the VOLVO drawing.
4.4.3 The SQE may ask for the submission of additional information. Prior to submission, suppliers should
contact the responsible SQE to determine if additional documentation is required. Proprietary documents
that cannot be submitted must be available for review. Suppliers may be required to travel to VOLVO
sites for review of proprietary documents.
4.4.4 The requirements associated with IMDS reporting are required for the full approval of the PPAP. To
avoid delays and deviations, suppliers should ensure that these requirements are achieved prior to the
SPR/PPAP. (Ref: section 5.10.5)
4.4.5 Suppliers will be notified via a signed PSW and/or a SSW regarding the status of the PPAP (approval,
rejected, or interim approval).
4.4.5 Exception to default PPAP level 4: Upon VOLVO request, suppliers may be required to submit a
Level 3 PPAP package for Key Components.
Page 20 of 53
SECTION 4.0
Document Requirements
Requirements Level 1 Level 2 Level 3 Level 4 Level 5
1 Design record R S S * R
2 Engineering Change Documents, if any R S S * R
3 VOLVO Engineering approval, if required R R S * R
4 Design FMEA R R S * R
5 Process Flow Diagrams R R S S R
6 Process FMEA R R S S R
7 Control Plan R R S S R
8 Measurement System Analysis Studies R R S * R
9 Dimensional Results R S S S R
10 Material, Performance Test Results R S S S R
11 Initial Process Studies R R S * R
12 Qualitified Laboratory Documentation R S S * R
13 Appearance Approval Report (AAR), if applicable S S S S R
14 Sample Product R R S * R
15 Master Sample R R R * R
16 Checking Aids R R R * R
Records of Compliance With Volvo Specific
17 R R S * R
Requirements
18 Part Submission Warrant (PSW) S S S S R
S= The supplier shall submit a copy of the records or documentation and retain a copy at appropriate locations
R= The supplier shall retain at appropriate locations and make available to VOLVO upon request.
*= The supplier shall retain at appropriate locations and submit to VOLVO upon request
Page 21 of 53
SECTION 4.0
Software Documentation Requirements
1 Statement of Work R
2 QDPR Compliance Matrix R
3 Communications Plan R
4 Document Traceability Matrix R
5 Responsibilities Matrix R
6 Skills and Training Matrix R
7 Customer Requirement Baseline Reference R
8 Software Requirements Specification (SWRS) R
9 Software Development Plan (SWDP) R
10 Software Development Schedule (SWDS) R
11 Risk Management Plan R
12 Risk Management List R
13 Progress Reports R
14 Complexity Report R
15 Software Quality Plans (SWQP) R
16 Software Design Desciption SWDD) R
17 Hardware/Software Interface Specification R
18 Requirements Traceability Matrix S
19 Node Function Implementation Plan (FIP) R
20 Software Test Plan (SWTP) S
21 Software Test Description (SWTD) S
22 Software Test and Verification Report (SWTR) S
23 Software Version Description (SWVD) S
24 Software Product Specification (SWPS) R
25 Software Configuration Management Plan (SWCP) R
26 Software Configuration Item List R
27 Software Worst-Case Analysis Report (SWWCA) R
28 Software Maintenance Plan R
29 Source Code R
30 SPICE Certification Report R
31 SPICE Assessment Action Plan R
S = The supplier shall submit a copy of the records and retain a copy at the appropriate location
R = The supplier shall retain a copy and make available to Volvo upon request
The minimum requirements for Software Approval include:
• Customer Requirements Baseline Reference
• Requirements Traceability Matrix
• Software Test Plan (SWTP)
• Software Test and Verification Report (SWTR)
• Software Version Description (SWVD)
Additional guidelines and a copy of the Software Submission Warrant (SSW) template are available on the
VOLVO Supplier Portal.
Page 22 of 53
SECTION 5.0
VOLVO SPECIFIC
REQUIREMENTS
Customer Specific Activities
Conformity of Cleanliness
Production Requirements Prototype Parts
In addition to the specific activities required by Frequently these tasks require close cooperation
Advanced Product Quality Planning, VOLVO between the members of the VOLVO and
has developed a select group of activities that supplier’s project team. Suppliers are
support the process of new part introduction encouraged to be full participants in these
serial production. These additional activities. All of the tasks required to support
requirements have been developed in response these activities should be included in the
to lessons learned in previous projects or to supplier’s project plan.
address specific customer needs.
Page 23 of 53
SECTION 5.0
5.0 VOLVO SPECIFIC REQUIREMENTS
5.0.1 In addition to the requirements described in the AIAG APQP reference manual, VOLVO requests the
planning and completion of the following cross-functional activities:
• Review of Technical Specifications
• Product Application Agreement
• Part Handling Review
• Process Audit
5.1.3 VOLVO has developed a unique system for control of technical documentation including the drawing.
This system uses the Part Version Report (PVR) rather than a drawing as the top level document. The PVR
contains the part and drawing revision information along with references to the technical information.
Suppliers should carefully review the PVR and all of the referenced documents to ensure a thorough
understanding of the technical requirements.
Page 24 of 53
SECTION 5.0
by VOLVO and the supplier. Signing the RTS signifies agreement by all parties that the Technical
Requirements, VOLVO Standards and General Specifications applicable to the part have been received, are
understood and are achievable.
5.1.7 The RTS provides a record of specification or production issues discussed during the part launch. It is
recommended that suppliers include a copy of this signed RTS with the PPAP document package. This
ensures that all issues raised during the RTS process are properly addressed during the PPAP review.
The PAA is designed to anticipate and 5.2.2 This process involves a joint review by the supplier
prevent problems related to the integration of and VOLVO of the performance requirements and the
supplier designed parts into the systems or physical installation of the component in the final truck
sub-systems of the truck. The process application.
provides an opportunity for the supplier to
review the performance of their product in 5.2.3 By signing the PAA, the supplier agrees with the
the final application. environment and application in which their product is to
be used.
Page 25 of 53
SECTION 5.0
5.4 SPECIAL CHARACTERISTICS
5.4.0 While all characteristics of a part are required to conform to specifications, there are a few
characteristics that are selected as special characteristics. Volvo has recently revised the specifications
regarding special characteristics. During the transition, special characteristics may be identified on drawings
or technical specifications using either of the following methods.
5.4.1 The selection criteria and guidelines related to special characteristics are based on the VOLVO
specification: STD 105-0007 “Special Characteristics Definition and Application”. This standard describes
the system currently used by VOLVO to highlight and grade critical characteristics appearing in drawings and
technical specifications. Special characteristics are identified using the symbols [CC] or [SC] next to a
feature in a VOLVO technical document.
5.4.2 The special characteristic symbols ([1], [2] or [3]) defined in STD 105-0001 ‘Critical Characteristics of
Design Products – Identification & Grading’ may still be present on some Volvo drawings or other
documents. These indications are valid and the characteristics shall fulfill the requirements stipulated in STD
105-0001. If the [1], [2], or [3] are present, the rules governing [CC] [SC] should be applied by the following
guide: [1] equals [CC] requirements, [2] or [3] equal [SC]. Symbols from STD 105-0007 and STD 105-0001
are not used together in the same document.
For all features identified as a special characteristic, the following requirement applies:
Cpk≥1.67 Cpk≥1.33
Electronic components Electronic components
Minimum requirement Cpk≥2,0* Minimum requirement Cpk≥2,0*
Process under
statistical control • Process appropriate checking Checking frequency adequate to
Normally distributed frequency demonstrate
• On-going Statistical Process • On-going Statistical Process
Control Control
• Ppk Analysis every 6 months • Compliance to capability
requirement
• Electronic or Automated Poka
Yoke
Process not under • 100% Inspection till agreed period
• Effectiveness verified once per
Statistical Control or for achieving process control
shift
Capability not • Plan for achieving control and
achieved • Volvo approved action plan for
capability
achieving Process Control and
Capability
*This requirement applies to all Electrical/Electronic components
5.4.3 The requirements related to special characteristics are also applied to all parts classified as Safety
Critical or Conformity of Production (COP). The specific application and any additional requirements related
to Safety and COP are detailed in the relevant sections of this document.
5.4.4 In addition to the special characteristics identified in VOLVO drawings or technical documents,
suppliers must identify any special characteristics related to their product. Suppliers should communicate
their standards for selecting and ranking critical or key characteristics and the methods used for designation
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SECTION 5.0
on drawings. Suppliers shall also define any special considerations for handling, assembly,
application, capability or use required to ensure safe, reliable performance of the product.
Governmental authorities, the automotive 5.5.1 Legal Requirements and Conformity of Production
industry and environmental organizations (COP) refer to individual components or systems that are
have developed guidelines and regulations directly connected to vehicle regulations. The vehicle
that are placed on vehicle manufacturers. approval in several countries is linked to valid component
These regulations apply both to the type approval at our suppliers since Volvo uses them to
customer vehicle and to the manufacturing obtain system and vehicle approval. Therefore, suppliers
processes. Ensuring compliance to these must be well acquainted with the regulations and legal
regulations is referred to as Conformance of requirements that apply to their components, both as
Production or COP. used within a vehicle and on a standalone basis (such as
an aftermarket part) on a worldwide level in order to
obtain the type approval of the supplied component.
5.5.2 VOLVO requires suppliers to follow the regulation to obtain their approvals as well as follow all valid
regulations related to COP during the part’s lifetime. By conducting business with VOLVO all suppliers agree
to comply with any and all such regulations. Each time the supplier changes the authority approval (new
extension, new amendment level or whatever the reason), the supplier will provide that information to
VOLVO 6 months in advance, since the system and potentially, vehicle certificates are impacted. Any update
of a certificate from authority to supplier, the supplier is required to immediately send a copy of that signed
document to Volvo.
5.5.3 VOLVO will during APQP/PPAP endeavor to confirm that the suppliers have a system in place to
record and document their own process of COP, so the COP approval continues to be valid, although
ultimately it is understood that this responsibility rests solely with the supplier. VOLVO will always require,
and all suppliers conducting business with VOLVO agree, that if a supplier is in a non-conformity situation
during COP testing that VOLVO is immediately informed by such supplier, and further that such non-
conformity is promptly corrected. By conducting business with VOLVO our suppliers agree that VOLVO may
at any time inspect the suppliers ability to monitor its COP system
5.5.4 For POWERTRAIN applications, and parts that have the potential to impact compliance, legal
regulations or features, such components are identified using the symbols [2R] or [3R] . These symbols
appear on VOLVO drawings or are stated within the related VOLVO technical specifications controlling the
part. The determination [2R] or [3R] grading is based on an assessment of how seriously the consequences
of noncompliance with the requirements for the characteristic in question, will impact VOLVO’s compliance
with the legal or governmental requirement. IT IS UNDERSTOOD HOWEVER THAT THIS ASSESSMENT
IN NO WAY RELIEVES ANY SUPPLIER OF THE RESPONSIBILITIES DESCRIBED IN SECTION 5.5.1.
5.5.5 Volvo standard STD 105-0004 defines the guidelines for grading characteristics. This standard
generally applies to components intended for POWERTRAIN applications (engines, transmissions and drive
axles), but may apply to any component of a vehicle.
5.5.6 All parts with features designated as [2R], [3R] are also considered “Key Components” and are
subjected to the same level of control. The designation of [2R] or [3R] differentiates the degree of
significance of the characteristic in question.
5.5.7 It is mandatory for [2R], [3R] parts to be inspected or tested and the necessary documentation
(inspection results, test reports, certificates) to be kept at the supplier for a period of time consistent
with the documentation retention policy. All inspections or tests required to ensure compliance to [2R],
[3R] regulation must be included in the control plan. A summary of the results from inspections or tests
should be communicated to VOLVO at regular intervals. Conformance to COP process requirements must
be respected during the entire product lifetime. No changes to product or process are allowed without formal
approval from VOLVO. No deviations are allowed on features designated as [2R].
5.5.8 When characteristics for regulatory compliance are identified the following requirement applies:
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SECTION 5.0
Cpk≥1,33 Cpk≥1,33
Process under On-going SPC data recording Inspection completed to control
statistical control (Control charts or electronic data plan (Results recorded maintained
Normally Distributed stored and available upon request.) and stored, available upon request.)
Ppk analysis conducted every 12 Ppk analysis conducted every 3
months years
• Machine or process 100% • Machine or process 100%
Process not under
automated checking surveillance. automated checking surveillance.
Statistical Control or
• Plan for achieving control and • Plan for achieving control and
Capability not achieved
capability capability
5.5.9 In the event of non-conformance of an identified characteristic or component escaping the supplier’s
location, the following actions must take place immediately:
• Notify the VOLVO buyer and SQE
• Containment at supplier, VOLVO locations and In Transit
• Short term corrective action
• Begin cause analysis
• Develop an action plan to recover full conformance
5.6.2 When required, cleanliness testing must be performed using the flushing method as defined in the
Volvo STD: 107-0002. Alternative testing methods must be approved by Volvo Product Development.
Suppliers are required to perform cleanliness testing at intervals that demonstrate adequate control of the
cleaning process.
Example of Cleanliness
Requirement Call Out
Not representative of
actual requirements
5.6.3 In addition, a cleanliness audit in accordance with STD: 107-0003 may be required by the assigned
SQE. The responsible SQE will provide the appropriate information if a cleanliness audit is required.
5.6.4 Even when cleanliness is not specified on the PVR, drawing, Technical Requirements or standards,
parts shall be delivered free from dirt, machining chips, burrs, or rust.
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SECTION 5.0
5.7 PROTOTYPE PARTS
5.7.1 To support design verification testing, or early build trials, suppliers may be required to deliver
prototype parts. By the VOLVO definition, prototype parts are any parts that are built on a production
process other than the final PPAP approved process. Prototype parts may be requested at different times
during the product design cycle. The requirements for the respective levels of prototype parts are:
The appearance requirements for CPOT may be waived based on agreement between Volvo and supplier
during the RTS process. (no chroming, no graining..)
Document and
product release
version
5.7.3 Suppliers are required to develop a Prototype Control Plan to support the production, inspection and
testing activity of parts manufactured according to the release stage of their technical documentation.
The prototype control plan should include all product features and characteristics of the product and include
any additional requirements from a Measurement Point plan (MP), or a Dimensional Control Plan (DCP) the
supplier may have received from Volvo Engineering for some components.
The objective of this control plan to ensure that the parts produced are fully conforming to the specifications
5.7.4 Prototype parts, where the part or any of the features of the part fall under the requirements for
Conformity of Production, Safety Critical or special characteristics, must meet the requirements as defined in
the related section of this manual. The section of the capability requirements chart “Process control
not achieved” shall be applied. All special features must be clearly identified in the Prototype Control
Plan.
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SECTION 5.0
Exceptions to these requirements (number of samples measured/ features measured) must be agreed prior
to the “Signing” of the RTS. All exceptions to the measurement requirements must be documented in the
RTS. Exceptions for functional requirements, must be identified in the Verification Report as “RTS not
measured” characteristic. The evidence of inspection, verification and measurements must be recorded in a
Verification Report and copies of the records forwarded to VOLVO prior to shipment.
5.7.6 For any prototype parts not achieving full compliance to the technical specification, shipment is not
authorized unless approved by VOLVO engineering and supported by an approved deviation.
5.7.7 All shipments of prototype parts must be clearly identified as a shipment of prototype parts using an
orange label with the word PROTOTYPE prominently displayed on the exterior of the shipping skid or
container. Specific details related to shipment guidelines, the prototype identification label and
documentation requirements can be obtained by visiting the VOLVO Supplier Portal or by contacting the
buyer that placed the order for those prototype parts (Prototype order or Quantity order) .
5.7.8 Prototype parts must be clearly identified with the part number, the part version and marking that allows
the part to be identified as a prototype after installation. The purpose is to identify prototype parts so they
are clearly identifiable in the production environment and on vehicles. The intention is to insure that
prototype parts can be easily differentiated from PPAP approved P release parts. Prototype specific
identification should be appropriate to the part and agreed between the supplier and VOLVO Engineering.
5.7.9 Suppliers will receive a PPAP purchase order, a tooling order for production tooling (depending on the
business arrangement), and a specific purchase order defining the quantity of CPOT parts required for the
current issue.
5.7.10 CPOT/IPD (In Plant Delivered) is the date defined by the project, when CPOT parts are required to be
received at the VOLVO using plant. Parts delivered under the CPOT/IPD process must be delivered and
received at the using facility by the In Plant Delivery date. The exact “In Plant Delivery” date will be
communicated in the purchase order for the CPOT parts.
5.7.11 Acceptance and use of CPOT parts by VOLVO does not imply production approval. Compliance to
the CPOT requirements do not replace the requirements for conducting the PPAP. Demonstration of
process capability is not required for CPOT parts, however, the CPOT process provides an excellent
opportunity to evaluate capability of the tooling prior to the SPR.
5.7.12 Unique requirements related to prototype parts specific to a VOLVO plant, business unit or region are
available on the supplier portal or by contacting the buyer.
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SECTION 5.0
5.8 REACH COMPLIANCE AND IMDS REPORTING
5.8.1 REACH is a regulation of the European Union, adopted to improve the protection of human health and
the environment from the risks that can be posed by chemicals, while enhancing the competitiveness of the
EU chemicals industry. REACH stands for Registration, Evaluation, Authorisation and Restriction of
CHemicals. This regulation went into effect on 1 June 2007.
5.8.2 To comply with the regulation, companies must identify and manage risks linked to the substances
they manufacture and market. For substances listed on the Candidate list which are manufactured or
imported in quantities of 1 tonne or more per year per company, manufacturers and importers need to
demonstrate that they have appropriately identified and managed the associated risks by means of a
registration dossier, which must be submitted to the European Chemicals Agency (ECHA).
5.9.3 Companies established outside the EU are not bound by the obligations of REACH even if they export
products into the European Union. The responsibility for fulfilling the requirements of REACH, such as pre-
registration or registration lies with the importers established in the European Union, or with the “Only
Representative” (OR) of a non-EU manufacturer established in the European Union.
5.8.4 Substance Declaration in IMDS and Substrack is a requirement for PPAP approval. IMDS (
International Material Data System ) is used to meet the obligations placed on automobile manufacturers,
and thus on their suppliers, by national and international standards, laws and regulations. Substrack is a
Volvo developed IT system that is connected to the IMDS database. The purpose of this system is to allow
for control of substances, material content and regulatory polymeric marking within Volvo products. The
Substrack process creates a link between the Volvo systems and compliance to the IMDS reporting
requirements. Tier 1 Suppliers are required to create an account in the IMDS system, designate a contact
person for IMDS reporting responsibility and create an environmental contact mailbox on the Volvo Supplier
Portal under Substance Tracking. When reporting in IMDS the only Volvo Group id number 46569 shall be
used.
5.8.5 The requirement for suppliers to do IMDS reporting will be found in the Part Version Report or
Technical Requirement of the part. When reporting is required, suppliers must log into the IMDS system to
report material content of products they supply. Data entered into IMDS is uploaded in the Substrack system
and the MDS information is checked at Volvo for approval. The requirements associated with IMDS reporting
are required for the full approval of the PPAP. To avoid delays and deviations, suppliers should ensure that
these requirements are achieved prior to the SPR/PPAP.
5.8.6 Additional information is available in the Volvo Standard STD 100-0006 and the following link:
http://supplierportal.volvo.com/vsp/int/en/E-Library/environment/Pages/environment.aspx
5.9.2 Suppliers may be required to implement a separate inspection activity at process start up that is
independent of the inspections and controls required by the control plan. The purpose is to verify the
affectivity of the control plan, and determine the capability of the production process. The application of this
additional control may be required by the VOLVO SQE for early production when a supplier’s performance
indicates that current controls are not adequate to identify and address problems prior to reaching the
customer. Shipments of products that have been through additional process controls should display
prominent notification on each shipping unit (box, package or skid).
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SECTION 5.0
5.10 AFTERMARKET PARTS REQUIREMENTS
5.10.1 The VOLVO name has become synonymous with the word Quality. Customers of VOLVO products
expect the same quality on Aftermarket parts, including repair and maintenance, as they expect from the
original equipment. VOLVO requires that the criteria of this manual apply fully to the production and delivery
of Aftermarket parts or products. This includes, but is not limited to, the planning for product realization
(APQP), approval process for new or changed parts (PPAP), changes to production process (PPCN), safety
parts requirements, and responsiveness to corrective action requests.
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SECTION 6.0
SAFETY MANAGEMENT
Protecting the Customer
Safety
Production
Responsibility Identification Management Traceability
Requirements
Audit
From the founding of VOLVO in the 1920’s, The primary objective is to develop products
quality and safety have been core values of that assist in preventing accidents from
the corporation. Since that time, the occurring or, in the event an accident does
continued commitment to the research and occur, to minimize the consequences for the
development of new and often unique safety drivers and others on the road.
solutions has made the VOLVO name
synonymous with safety around the world. The supplier’s contribution to safety lies in
developing innovative solutions,
Today, Quality, Safety and Care for the implementing safety features and producing
Environment continue to be the core values fully conforming products. The VOLVO
of the organization and form a foundation for safety management program focuses on
all business practices including the both the suppliers’ management systems,
cooperation between VOLVO and our and product quality related to safety.
suppliers.
Safety Management applies to a part,
The VOLVO definition of safety not only function or feature when a non-conformance
includes the safety of the immediate user of related to the product would create a safety
our products, but also understanding the hazard.
entire scope of potential impact of our
products on society.
http://www.volvo.com/group/global/en-gb/volvo+group/ourvalues/safety/safety.htm
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SECTION 6.0
6.1 DEFINITION
6.1.1 Safety requirements are determined based on the potential of a feature, product or system to create a
personal hazard to any person in contact with the products or effects caused by the product. A Safety
Customer Effect is considered when a danger can lead to injuries to vehicle operator, passengers, other
travelers, passers-by or maintenance personnel.
6.1.2 The activities related to safety management are required if any feature of a part is identified as having
an impact on safety, the part is considered safety critical. Suppliers of a safety critical part are categorized
as a Safety Part Supplier. Safety Critical related features are designated by the presence of the symbol [CC]
or [1] next to the feature on the drawing or in a specification.
6.2 RESPONSIBILITY
6.2.1 The production of safe, fully conforming products to the VOLVO Group companies is the supplier’s
responsibility and is part of the supplier’s contractual commitment. Any assistance provided by VOLVO does
not in any way limit the supplier’s responsibility to supply parts that conform to all technical specifications,
standards, regulatory, contractual and legal demands.
6.2.2 Suppliers are required to conduct a criticality analysis for features of the product design and production
process that could result in a safety effect. For suppliers having design responsibility, special characteristics
related to safety must be clearly identified within their design specifications, verification/validation plans,
drawings and technical documentation. Suppliers who are design responsible for products impacting safety
are required to develop System, Sub-System, Design and Process Failure Modes Effects Analysis to assist
in the analysis. Volvo must be notified of any product features or functions where the potential failure mode
and associated customer effect are assigned a high severity score (9 or 10). (Severity for any features
identified by Volvo with a [CC] or [1] must have a severity scored or a 9 or 10 on the suppliers FMEA).
6.2.3 Suppliers are responsible to ensure that all sub-suppliers and contractors are aware of and comply with
the requirements related to safety requirements. Tier I suppliers must have procedures and practices to
ensure an adequate level of control and requirements are deployed at all suppliers or sub-suppliers whose
product or processes could have an effect on safety related features.
6.3.2 A new standard for identifying and grading critical characteristics, STD 105-0007 “Special
Characteristics Definition and Application”, has been released and is effective for all Volvo drawings,
functional requirements and Technical Requirements. Drawings, Functional Requirements or Technical
Requirement developed before 1 Sept 2015 may follow Volvo standard Std 105-0001 ‘Critical
Characteristics of Design Products – Identification & Grading’.
PRODUCT IDENTIFICATION
6.3.3 The methods used for marking lot/serial numbers on safety critical parts must support identification,
traceability and failure investigation through all phases of the products life. In principle, the serial number or
lot number should be applied to the actual part and preferably should be easily visible when mounted on the
vehicle. When feasible, the [CC] symbol must be included on the part label. This would apply if the drawing
is marked with a [CC] or [1] symbol.
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SECTION 6.0
6.3.4 Unless otherwise specified in product documentation, the preferred method for marking is:
• Item serialization
• Bar code (In Accordance With VOLVO STD 103-0013 or VOLVO approved alternative)
• Recording of safety critical product or process parameters (Preferred)
• Recording OK/not OK is acceptable with evidence of 100% effectiveness
6.4.2 Capability requirements for parts identified with [1] [CC] characteristics are described below:
Critical Characteristics
level 1, [CC]
Cpk≥1,67
Cpk≥2,0 for electronic components
Process under statistical control
Normally Distributed • Process appropriate checking frequency
• On-going Statistical Process Control
• Ppk Analysis every 6 months
• Electronic or Automated Poka Yoke
Process not under Statistical • Effectiveness verified once per shift
Control or Capability not achieved • Volvo approved action plan for achieving Process Control and
Capability
6.4.3 Data records resulting from SPC, automated checking, and inspection results must be available for
download upon request by the VOLVO SQE. The data must include identification of the production lot or
serial number information.
6.4.4 In addition to the demands detailed in the table above, the supplier must apply the following
requirements on the shop floor;
• Identification of the operations which have a direct or indirect influence on safety feature
• Clear signs or placards defining the characteristic and potential effects of non-compliance
• Training status and authorization for all operators working on safety feature related workstation
• Rework of EE components is not allowed*
* This requirement does not apply to remanufactured electrical or electronic components.
6.4.5 During the APQP, Process Audits or PPAP activity, the VOLVO SQE will verify the evidence of
completion and compliance to these requirements for concerned products.
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SECTION 6.0
6.5 SAFETY MANAGEMENT AUDIT
6.5.1 Suppliers of safety critical components or assemblies must have safety system requirements
embedded in their quality management system. Suppliers must be able to demonstrate they have the
organization, systems, processes, and competencies to manage the VOLVO requirements related to safety
critical features.
6.5.2 VOLVO has developed and uses a technical audit to evaluate the Safety Management Systems of
suppliers of safety related parts. This audit evaluates the presence of an adequate management system and
the capabilities to properly manage safety parts through-out the production process. A Safety Management
Audit (SMA) will be conducted during the sourcing process and potential suppliers are required to achieve a
passing score prior to the award of business.
6.5.3 Suppliers that achieve a passing score but do not achieve the preferred 90% are required to develop a
detailed action plan with a timeline for achieving the 90% score. This plan must address all audit findings.
After achieving a 90% score, suppliers are re-audited periodically to ensure that the SMA systems and
processes impacting quality remain in place. VOLVO reserves the right to conduct a Safety Management
Audit at any time following a major quality spill or recall.
6.5.4 A copy of the Safety Management Audit template is available for review on the VOLVO supplier portal.
6.6.2 In addition to component/materials traceability, the system must be capable of providing the production
history of a lot or serial number. This history must include:
- Rework operations or activity*
- Product and process special characteristics
- Test records
- Process parameters influencing conformance
- Machine settings influencing conformance
- Maintenance activity of machines, equipment, jigs, gages and test equipment
- Operators and personnel qualification records for operators performing the work
6.6.3 If product is controlled in lots or batches, a risk analysis related to severity of non-conformance and
probability of occurrence must be conducted and used in establishing the lot sizes to minimize the impact of
product recall.
6.6.4 The minimum requirement for storage of information related to safety critical parts is 10 years from date
of manufacturing. Any additional requirements related to storage related to applicable legal requirements
must be maintained.
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SECTION 6.0
6.7.2 A VOLVO SMA on-site audit will be conducted at the supplier of Safety Critical “pass through parts”.
The VOLVO safety auditor will conduct the audit focusing on Chapter 1 – “Company Management” and
Chapter 4 – “Supplier Chain Management”.
6.7.3 VOLVO requires Tier I suppliers to have an active Safety Management Audit process for their
suppliers. For those suppliers that do not have an audit process of their Safety Critical suppliers, VOLVO
does offer assistance to Tier I suppliers in developing a Safety Management Program. This assistance may
include conducting a joint audit at a Tier II supplier. The Tier I supplier is responsible to continue the SMA
program and follow up on all action items initiated during the original audit. VOLVO does not assume
responsibility for the supplier’s SMA program, audit results, or follow-up activity. All responsibility for the
SMA program and the quality of safety related products remain the responsibility of the Tier I supplier.
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SECTION 7.0
PRODUCTION REQUIREMENTS
Supporting Processes
Laboratory Record
Packaging Warranty
Requirements Retention
While the production operations ultimately The processes described in this section do
determine the quality of product, ensuring not directly determine or improve product
consistent quality also depends on the quality, but failure of these processes has
capability of supporting processes. the potential to adversely affect product
quality.
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SECTION 7.0
7.1 PRODUCT PROCESS CHANGE NOTIFICATION (PPCN)
All proposed changes to the product, production 7.1.1 In accordance with the ISO/TS
process, material or suppliers after PPAP must be 16949 standard, the PPAP guidelines,
submitted to VOLVO for approval using the PPCN and VOLVO Purchasing conditions, a
process. Requests for change must be submitted supplier cannot implement a change to
at least 12 weeks prior to the introduction of the a product or production process after
change. PPAP approval, without prior approval
from VOLVO.
7.1.2 The purpose of this requirement is to prevent quality & delivery issues resulting from unapproved,
untested changes or modifications after PPAP approval. This applies, but is not limited to, the following
cases:
• Transferring of the production line: partly or • Change at sub-tier suppliers that affect fit,
totally; to a new or existing location, plant or form or function of the product
building • Renewal of non-consumable tooling
• New production layout or changes to production • Change to the raw material
line • Outsourcing all or part of production to a
• Change of a sub-tier supplier sub-tier supplier
• Changes of a process at a contract supplier, • Request for change to product design
(surface treatment, machining…..) including dimensions, tolerance, function,
• Packaging changes or repackaging operations appearance
7.1.3 The supplier desiring a change shall submit a completed Product and Process Change
Notification form to the VOLVO buyer with a copy sent to the Supplier Quality Engineer as soon as
the modification project is known, and at least 12 weeks prior to the intended Start of Production.
Some components or commodities may require a longer time to achieve full approval of changes (ex.
Electronics) As a general rule, suppliers should notify VOLVO of required changes as early as possible and
obtain agreement on the implementation timing. Suppliers may be required to submit additional information
to support evaluation of the proposed change (Product Validation Testing, Dimensional or Functional
Reports). The PPCN form is available on the supplier portal.
REQUESTS FOR CHANGE MUST BE SUBMITTED USING THE PRODUCT AND PROCESS
CHANGE NOTIFICATION (PPCN) A MINIMUM OF 12 WEEKS PRIOR TO THE PROPOSED
CHANGE.
7.1.4 Since VOLVO functions as a global company with manufacturing functions on most continents,
suppliers must be prepared to support the impact of a change request at all impacted VOLVO facilities.
Suppliers making a process or product change must be capable and willing to provide information and
resources required to secure product quality and uninterrupted deliveries.
7.1.5 Introduction of changes without VOLVO approval may result in any or all of the following
actions:
• All costs related to correcting the situation created by an unauthorized change will be charged back
to the supplier.
• The supplier’s 3rd party certification body will be formally notified that the supplier is not following
quality system or customer requirements.
• Supplier will be required to complete corrective action and demonstrate effective controls to prevent
recurrence.
• Supplier may be placed on hold for new business.
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SECTION 7.0
7.1.6 After receipt by VOLVO, the request is submitted to a team for analysis. Based on the impact to
VOLVO and the risk associated with the change, the PPCN may have one of the following decisions:
• Authorize the supplier modification.
• Ask to adapt the content of the supplier modification.
• Ask the supplier to delay the implementation until extra actions/verifications are performed. (Actions
include, but are not limited to, audits, safety stock, testing, etc. …)
• Ask the supplier to cancel the proposed modification.
7.1.7 Once approved by VOLVO, suppliers will be notified by an official letter. Upon receipt of the approval
letter, suppliers should implement the modification project according to the agreed implementation plan.
7.1.8 The level of PPAP documentation required to support the introduction of the change will be determined
by the SQE. Authorization to start shipping (with the changes implemented) is only granted via the return of
the signed PSW and/or SSW following PPAP approval.
7.2.2 Suppliers to Volvo Truck must complete and submit a Global Deviation Request using the Global
Deviation/SREC Request form. The completed form may be submitted by email to the responsible SQE,
buyer or to the email location indicated on the deviation form. This form is available on the VOLVO Supplier
Portal in the Serial Production section of the Quality E-Library or by accessing the link below:
http://supplierportal.volvo.com/vsp/int/en/E-
Library/Quality/3P_and_Powertrain/serial_production/Pages/Serialproduction.aspx
7.2.3 Requests for approval are reviewed by a cross functional team comprised of the Volvo responsible
design engineer, the buyer, and the assigned SQE. If the deviation is approved, the supplier will be emailed
a copy of the notice of approval.
7.2.4 Suppliers to VBNA must complete template and follow the process defined on the supplier portal in the
Nova Bus section.
7.2.5 All shipments made under a deviation should be identified on the exterior of the shipping container.
Specific labelling type should be agreed between the supplier and the SQE. Any label should include the
deviation approval number. Suppliers requesting a deviation must complete an 8D response identifying the
cause, corrective action, and measures taken to prevent recurrence.
7.3.2 When lot control is utilized, the system must establish and maintain one-to-one relationship between a
lot/batch traceability number and a certain quantity of produced parts. If a traceability number, other than the
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SECTION 7.0
serial number, is used for identifying serialized parts, a one-to-one relationship between the traceability
number and the serial number must be maintained.
7.3.3 The extent of definition and control shall be based on risk analysis of the product and the
potential impact to customers. Suppliers are responsible to ensure that the lot traceability system
maintains its integrity through the entire supply chain, including raw material, purchased
components/products, and sub contracted operations.
7.5.2 VOLVO Purchasing reserves the right to have direct access to sub-tier suppliers and processes that
could have significant impact on final product quality. This will generally concern technical processes like
surface treatment, heat treating, forging, casting etc. Please check with your SQE to determine if your sub-
tier or contract suppliers would fall into one or more of these categories. Access to sub-tier suppliers or
approval of sub-tier suppliers by a VOLVO Technical Specialist, does not change or reduce the supplier’s
responsibility for quality of products supplied by those sub-suppliers.
7.5.3 VOLVO Purchasing requires suppliers to use the AIAG Production Part Approval Process (PPAP) and
that this requirement is applied to sub-tier suppliers of products to be used in VOLVO products. Suppliers
have the responsibility for managing the PPAP at their suppliers and maintain evidence of compliance.
7.5.4 Once a part is approved, changes at sub-tier suppliers that affect fit, form or function must be
documented and approved by VOLVO using the Product Process Change Notification process.
7.6 PACKAGING
7.6.1 In support of the VOLVO commitment to protecting the environment, VOLVO has developed a process
for returnable packaging and integrated logistics system. Suppliers are expected to package components
according to packaging instructions that are agreed to and approved between Volvo and the supplier before
shipment to Volvo. Suppliers are required to provide appropriate storage and protection for VOLVO
emballage while under their control.
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SECTION 7.0
7.7 WARRANTY
7.7.1 Responding to field warranty claims remains a top priority at VOLVO. When Field Failures are
determined to be the result of a supplier’s product, suppliers will be notified through receipt of a warranty
claim. It is expected that suppliers will fully participate in the investigation, root cause analysis and corrective
action when field failures are identified. Suppliers should have an established process for the handling,
analysis, investigation, reporting and corrective action of customer field returns. VOLVO has developed and
conducts a Warranty specific process audit of supplier’s capability to manage customer field returns.
7.7.2 If the non-conformance is generated by a supplier, a VOLVO warranty department may call the
responsible supplier for immediate correction or replacement of products. The conditions defining response
and responsibility are included in the Purchasing conditions, purchasing agreement and/or warranty charter.
A copy of the warranty charter is included as part of the Request for Quotation.
The above time periods shall be regarded as minimum. Retention periods longer than those
identified above may be specified by an organization in its procedures.
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SUPPLIER PERFORMANCE
MEASUREMENT
AND CORRECTIVE ACTION
Responding to Problems
Quality
Nonconforming Supplier Improvement
Performance
Material Scorecard Process Audit
Measurement
Low
Continuous Field Quality
Performing
Improvement Issues
Suppliers
VOLVO recognizes that the performance of Even under ideal conditions and careful
the supply base has a direct and immediate preparation, problems may occur. In addition
impact on organizational performance. In to performance, VOLVO measures a supplier
response to this, VOLVO has developed a based on their cooperation in aggressively
system for the measurement and evaluation seeking to resolve problems. Suppliers are
of supplier performance. The indicators evaluated on the promptness of the initial
resulting from this process are compiled response when notified of a problem, the
every month and are reviewed and evaluated timeliness of subsequent actions, and the
at all levels of the VOLVO organization. effectiveness of actions taken to resolve the
These measurements are available for problem.
review on the Supplier Scorecard on the VOLVO invites suppliers to work as partners
supplier portal. in the problem solving process.
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8.1 MANAGING NON CONFORMING PARTS
INSPECTION REPORTS
8.1.1 It is in the interest of both VOLVO and the supplier, to identify and address non-conforming parts as
quickly as possible.
In the event non-conforming parts or 8.1.2 Suppliers shall take all necessary actions to
materials have been identified at a VOLVO respond to nonconforming product that reach a
location, suppliers will be notified using an VOLVO facility (production site, warehouse, etc).
INSPECTION REPORT [IR]. The Inspection Every effort is taken to investigate and document non-
Report is sent to an internet location along conformances and to notify the supplier immediately.
with an email to the supplier’s quality When possible, suppliers will be given early notification
contact. of a problem prior to the issuing of an Inspection Report
(IR).
8.1.3 VOLVO has developed a set of guidelines used by VOLVO plants in determining the non-conformance
quantity for each Inspection Report. These guidelines are referred to as the “Inspection Report Golden
Rules” and are available on the supplier portal.
8.1.4 All costs (administrative, sorting, handling, shipping, and rework) associated with addressing a non-
conformance will be the supplier’s responsibility. These costs may include any secondary costs incurred by
VOLVO resulting from a non-conformance. These include the costs associated with tear down, reassembly,
re-testing, and logistics support.
8.1.5 Under normal circumstances, suppliers are expected to respond immediately to any nonconformance
and ensure that all receiving plants are protected within 24 hours. Suppliers are required to notify VOLVO
immediately if it is suspected that non-conforming material has been shipped to a VOLVO facility.
8.1.6 Depending on the type of non-conformance and material status, supplier parts may be sorted,
reworked or adjusted. Supplier approval is requested before any rework or adjustment will be performed,
except in circumstances where support of production need requires immediate action. Suppliers should be
prepared to take any or all of the following actions after nonconforming material are identified at a VOLVO
facility.
• Expedited replacement of nonconforming material
• Provide resources to perform required sorting or rework
• Provide third party sorting resources
• Authorize VOLVO to begin third party activities on the supplier’s behalf
• Provide instructions and acceptance criteria required to support inspection, sorting, or rework
• Product specific gaging
8.1.7 VOLVO has agreements with third party sorting companies who are capable of providing sorting
activity on the part of the supplier. All costs associated with work and materials associated with the activity
of this third party are the supplier’s responsibility. Suppliers have the option to use this service or to contract
a third party to do sorting or rework on their behalf. Third parties selected by the supplier must be approved
by VOLVO prior to starting any sorting or rework.
8.1.8 If not used by VOLVO under deviation, after rework or after repair, nonconforming parts or material will
be “returned to supplier” or “scrapped at VOLVO” based on supplier’s direction.
8.1.10 Each time a non-conformance or a defect has been documented, the causes for the problem must be
investigated and reported. It is recommended that suppliers respond using the VOLVO 8D format. A copy of
the 8D template is attached to each Inspection Report. A copy is also available in the e-library on the
VOLVO supplier portal. Suppliers may respond using their corrective action format as long as it includes
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containment, cause analysis, problem correction, and problem prevention. To avoid delay and extra work,
suppliers should submit their corrective action response format for approval to their SQE.
8.1.11 On a continual basis, supplier performance is monitored for PPM Level, QPM level, delivery precision.
8.1.12 In addition to the cause and corrective action conducted during the 8D process, suppliers should
conduct Root Cause Analysis for all major issues. Root Cause analysis requires evaluation of the
weaknesses within the organization processes or systems that allowed the problem to occur. Root Cause
generally requires management action to address the underlying systems or processes.
8.1.13 If the resolving time lasts longer than 20 days, the supplier must reach an agreement with SQE.
8.1.14 In addition to
correction of the
documented problem,
suppliers shall apply the
lessons learned to all
similar products or
processes. (Horizontal
Deployment). Permanent
countermeasures for all defect
categories should be
implemented for all parts and
processes.
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8.2.2 The supplier’s performance is calculated for a calendar month and the scorecard is updated during the
first half of the following month. Information about the latest update can be found under
“information/sources”. The scorecard shows information for the prior three months, with the ratings
calculation based on a three month rolling average. Information for other periods is available using the ‘View
Performance Breakdown’ page.
8.3.2 The QPM measurement includes the actual number of parts rejected, the number of Inspection Reports
written and the value of rejected parts compared to the value of parts delivered compensates for anomalies
inherent in the PPM calculation. Example: If a supplier had 1 part from a shipment of 10 pieces rejected
during a three month period, the resulting PPM for that period would be 100,000. The related QPM for this
same three month period would be:
PPM: 20 + NCp: 5 + IR: 0 + V/V: 20 = QPM: 45
The measurement criterion for each measureable is defined in the tables below:
Parts Per Million – The number of parts rejected, divided by the number of parts delivered multiplied by 1
million.
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Inspection Report: Refers to the total number of Inspection Reports issued to a supplier during the three
month window.
Non-conforming Parts: Refers to the total number of parts returned during the months being evaluated.
Volume Value: Is the percentage calculated by dividing the cost of returned material for a three month period
by the total value of products delivered during that same time period. This calculation compensates for the
situation where suppliers may have a large number of rejects of very low value products while successfully
supplying high value products but at a lower volume.
Additional Information
8.3.4 In addition to performance information, the scorecard contains other important information for the
supplier. This includes information related to:
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8.4.2 In addition to the situations listed, the production processes of components that have been identified as
critical to the safe, reliable function of a vehicle are subjected to annual audits. These audits are to ensure
that the production processes used during the “Significant Production Run” remain unchanged and capable
of delivering consistent quality products.
8.4.3 VOLVO reserves the right to perform process audits whenever it is deemed necessary. Suppliers will
be given reasonable advance notice of a pending audit. A copy of the Process Audit template used by
VOLVO in conducting the audit is available for review on supplier portal.
8.4.4 One or more process audits may be required during the development and launch phases of the
introduction of a new product or process. The respective VOLVO SQE will communicate this requirement to
the supplier during the development of the APQP activities. In addition to audits conducted by VOLVO,
suppliers are expected to routinely conduct internal audits of their production processes. Records of any
findings from internal audits and actions taken in response to findings should be available for review during
the VOLVO process audit.
8.5.2 In addition to responding to identified nonconformances, suppliers should use statistical data
to continually evaluate and refine their processes. This evaluation should include analysis of quality Out
Of Control indications, high PPM, scrap, downtime, and warranty failures. The clear objective of this analysis
must be reduction of variation with the finished product. The supplier shall have on-going, active
improvement projects that target two or three of the largest problem areas and be able to
demonstrate a positive trend in reducing incidents and repeat occurrences.
8.6.2 Suppliers will be notified of the potential inclusion in the LPS process by a warning letter sent to the
supplier’s Quality department. The letter will include the reason or reasons a supplier is being considered for
entry into the LPS process.
8.6.3 The LPS procedure provides a clearly defined guide to the analysis, actions and monitoring that will
take place while a supplier is engaged in this process. Supplier improvement activities are initiated and
monitored through a three-stage elevation process. Each stage has defined criteria for entry and exit and
identified actions to be completed during the stage. Exit criteria is based on improved performance results
and implementation of process improvements. Suppliers that do not meet the criteria for a stage by the
target completion date are elevated to the next LPS stage level.
8.6.4 Each time the supplier is elevated to a higher stage, the actions required will be those of all previous
stages, plus the additional actions required by the new stage. At any time that the exit criterion is met for a
specific stage the supplier is moved to the “Monitoring” status. A supplier can be placed in the LPS based on
performance for an individual part number, multiple part number bases or organizational performance.
Supplier performance is tracked based on the VOLVO assigned Parma code.
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8.7 FIELD QUALITY ISSUES
8.7.1 It is in VOLVO’s and our supplier’s best interest to solve Field Quality Issues as quickly as possible.
Therefore, once the supplier is notified of a deviation in the field that is potentially related to supplier
delivered parts, the supplier is requested to provide all needed support.
8.7.2 Pre-investigation
When VOLVO detects an issue in the field and assess that a purchased part is either directly or indirectly
involved, VOLVO will request supplier support in order to investigate the case and fine tune the problem
description (1D phase). VOLVO expects the following outcome from the Pre-investigation:
• Parts Analysis
• Initial Cause Analysis
• Estimated failure occurrence
• Proposed Containment Action
Following the Pre-Investigation VOLVO will decide the most appropriate Solving Process.
• Quick Solving Process. QSP is applied when the failure is related (directly or indirectly) to a
supplier part that is found to deviate from the technical specifications for the part. (e.g.
manufacturing process deviation)
o The solving process will be led by the supplier and Volvo will monitor progress of the
implementation and verification of the solution.
o An 8D report is required for all QSP
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o Expected Solving Lead-Time is the same as for Inspection Report, see 8.1
• Quality Journal. The QJ process is applied for critical and complex cases where the problem is
determined to be related to design or processes where a supplier part or product is involved.
o The supplier will be notified by an official letter of the opening of a QJ
o The QJ will be led by VOLVO, the supplier is expected to take an active part in the cross-
functional work
o Expected Solving Lead-Time is communicated in the QJ notification letter
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Glossary
AIAG – Automotive Industry Action Group
APQP – Advanced Product Quality Planning
[CC] – Critical Characteristic
CG – Concept Gate
COP – Conformity of Production
Cpk – Capability Analysis Index
CPOT – Conforming Part out of Tool
CPOT/IPD – Conforming Part Out of Tool/ In Plant Delivery
DCP - Dimensional Control Plan
DG – Development Gate
DVP - Product Development Process
ECHA - European Chemicals Agency
EE – Electical Electronic
EG – End Gate
E-library – A library of documents and procedures on the VOLVO Supplier Portal
ERP – Enterprise Rsource Planning
EU – European Union
Fault Frequency – Measure of product failures occurring on product after delivery to customer
FDG – Final Development Gatre
FIFO - First In/First Out
FIG – Final Industrialization Gate
FMEA – Failure Modes Effects Analysis
IDM -
IMDS - International Material Data System
Index Audit – An audit conducted on a technology related production process
IR - Inspection Report
Key Element Procedure – A series of guideline procedures for companies doing business with VOLVO
LPS – Low Peforming Supplier
MP - Measurement Point Plan
MRP – Material Resource Planning
OEE - Overall Equipment Effectiveness
OR - Only Representative
PAA – Part Application Agreement
PHR – Part Handling Review
PPAP – Production Part Approval Process
PPCN - Product Process Hange Notification
Ppk – Performance Analysis Index
PPM – Part Per million
Product Audit – Audit of samples taken from production process
PSW – Part Submission Warrant
PVR – Part Version Report
QDPR - Quality and Development Process Requirements
QJ - Quality Journal – Volvo internal problem solving process for field failure issues
QPM - Quality Performance Measurement
QSP – Quick Solving Process: Problem solving process for field issues related to manufacturing processes (not design)
REACH - Registration, Evaluation, Authorisation and Restriction of Chemicals
RFQ – Request for Quote
RG – Release Gate
RTS – Review of Technical Specification
[SC] – Significant Characterisitic
SEM – Supplier Evaluation Module
Service PPAP - Service Production Part Approval Process
SOW – Statement of Work
SPC – Statistical Process Control
SPICE - Software Process Improvement and Capability dEtermination
SPR – Significant Production Run
SREC – Supplier Request for Engineering Change
SSEM – Short Supplier Evaluation Module
SSW – Software Submission Warrant
Stopping Parameter – Issue in SEM where failing score eliminates supplier from consideration for business
SW - Software
SWTP - Software Test Plan
SWTR - Software Test and Verification Report
SWVD - Software Version Description
TR – Technical Requirements
VBNA - Nova Bus and Prevost Bus
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Revision Record
EDITION REVISIONS DESCRIPTION
06-2010 Integration of VOLVO Powertrain, VOLVO Buses, Prévost and Novabus in the scope of
application.
NO MAJOR CONTENT CHANGE:
• Wording clarifications all along the document.
• Reworked chapters :
Acknowledgement page,
Conformity of production (COP)
Special characteristics
Lot traceability,
Record retention,
• Added chapter: Laboratory requirements APQP reviews, Software,
• Removed: Appendixes, reference to toolboxes
01-2016 SQAM now includes Volvo Bus North America. This includes both Nova and Prevost.
Additional information regarding the suppliers responsibility to name a Super User.
New chart for Performance Expectations
Highlighting for requirements changed to be more visible.
New chart illustrating the relationship between DVP timing and APQP reviews.
4.3.8 PPAP notice to suppliers via official notice
5.1.1 Revised paragraph defining RTS process.
5.4.1 – 5.4.2 Revision to include application o f [SC] and [CC].
Changes to critical and special characteristics revised to include Action pan and regular
Ppk analysis.
5.5 Section on COP rewritten.
5.6 Section regarding cleanliness requirements revised to be consistent with the
Standard
5.8 Section CPOT/IPD rewritten to be consistent with new process
5.10 Section rewritten to better define IMDS requirements
6.2.2 Sentence added to include requirement for notification of failure modes with
potential of high severity.
6.3.3 New requirement for Critical Characteristic making on the part label for parts with
[CC] classification.
7.1.3 – 7.1.4 Changes to requirements regarding deviation approval.
7.5 New link to packaging instructions
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Fourth Edition
May 2016