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IAQG General Assembly San Diego, April 7, 2006
Supply Chain Process Capability & Product Realization Process Strategy Streams IAQG General Assembly San Diego, April 7, 2006 Barbara O’Dell The Boeing Company IAQG Stream Leader Supply Chain Process Capability Bernard Lauras Airbus European Sector leader Product Realisation Process
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Sub Tier Control as a Source of Risk To Regulators and Customers
No Change From Montreal Poor Control of Sub Tiers is viewed as a Risk Methods used by Suppliers to Control Sub-Tiers are not well understood Source of Non-Conforming Product Supplier doesn’t know how to control their (sub-tier) suppliers Sub Tier system insufficient to detect & prevent non-conformance Reduced level of interaction with Sub Tiers compared to with suppliers Part of the reason we perceive risk is that suppliers and subtiers are the source of non-conformance, but in addition, we don’t understand the methods used one or more layers down from us. One of the reasons this is so is that we lack visibility of the activities deep in the supply chain. If a company, such as Boeing or Airbus, has 100’s of suppliers, and those suppliers have 100’s of suppliers, then the second tier down will have 10,000 to one million suppliers. It’s not possible to have deep visibility of them all In addition, there is a lack of “transparency” in supplier control methods. In contrast, the international oversight system of other parties has created common terminology and expectations. I know what is happening in Asia because of the common language we use to describe the effort and the means by which the efforts are tracked. In supplier control, we don’t share such common methods and terminology to describe commonly performed tasks. As you can see on the right, the existence of common standards could also help benefit some suppliers whose supplier control program is weaker than industry practices Please note that this work I s a draft document, not yet reviewed by the IAQG team. Few industry standards and Best Practices published on how to perform excellent supplier control . No common vocabulary or scoring (Lack of Transparency) (Lack of Visibility)
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SCMH provides a framework for organizing and integrating our work
No Change From Montreal Stand alone requirements (9102, 9131, 9103, etc) 9100 Requirements Supply Chain Mgmnt Handbook Industry best practices on how to meet requirements Supplier Mgmnt Life Cycle Supplier Selection Pre Production Validation Ongoing Approval Change Mgmnt
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Supply Chain Process Capability
Name changed from Sub Tier Process Control No Change From Montreal Often, the value stream includes companies operating at many levels, and one standard should be consistently applied Ideal Stream Typical Stream OEM OEM First Tier First Tier OEM Sub Tier Sub Tier Sub Tier First Tier
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& Capability Assessment Verification & Acceptance
SCMH chapters have been renumbered and include Product Realization Activities 3.0 New Product Introduction 1.0 Supplier Selection & Capability Assessment 2.0 Requirements and Flowdown 4.0 Process Control 5.0 Product Verification & Acceptance 6.0 Controlling Non-Conf Product 7.0 Work Transfer Management 9.0 On going Approval And Maintenance 8.0 Supply Chain Mgmnt and Performance Measures 10.0 Program Management In work by Product Realization Stream In work by Supply Chain Process Capability Stream
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For every “chapter” in the Handbook We’ll follow this roadmap
Phase 1: Collect aerospace and other industry best practices, standardize the knowledge & agree on core requirements Phase 2: Create best practice material first, then mature into a guideline or to an industry standard document (910X standard). Maturity assessment may be developed here. Implementation Process should be defined here (pilot phase as required). Phase 3: Standardized training provided by industry accepted trainers Phase 4: Implementation Process. Depending on guideline vs 910X decision, the document may be deployed company by company, or by standardized audit checklist, or by industry certification as part of the ICOP/9104 system. Implementation must include maturity assessment.
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Supply Chain Process Capability have been tasked Chapters 1 and 2
3.0 New Product Introduction 1.0 Supplier Selection & Capability Assessment 2.0 Requirements and Flowdown 4.0 Process Control 5.0 Product Verification & Acceptance 6.0 Controlling Non-Conf Product 7.0 Work Transfer Management 9.0 On going Approval And Maintenance 8.0 Supply Chain Mgmnt and Performance Measures 10.0 Program Management In work by Product Realization Stream In work by Supply Chain Process Capability Stream
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Chapter 1 - Supplier Selection and Capability Assessment
IAQG SCMH Chapters Chapter 1 - Supplier Selection and Capability Assessment Supplier Selection & Capability assessment Requirement & Flow down New Product Introduction Process Control Product Verification and Acceptance Controlling Non-Conf product Work Transfer Management Supply Chain Mgt and Performance Measures On going Approval & Maintenance Project Management O Supplier Selection & Capability assessment Requirement & Flow down New Product Introduction Process Control Product Verification and Acceptance Controlling Non-Conf product Work Transfer Management Supply Chain Mgt and Performance Measures On going Approval & Maintenance Project Management O Supply Chain Processes Sales Volume & Option Forecasting Sales Volume & Option Forecasting Contract requirement flow down Contract requirement flow down New product introduction / New product introduction /LCM SC design & major Components sourcing SC design & major Components sourcing Suppliers sourcing selection & qualification Suppliers sourcing selection & qualification Sales & Operation Planning Sales & Operation Planning Manage the Supply Chain Manage the Supply Chain Master Scheduling & sequencing Master Scheduling & sequencing Performance Monitoring and Decision support Performance Monitoring and Decision support Planned change management Planned change management Supplier Development Supplier Development We took the definition of a supply chain: « That collection of industrial processes which lead to the arrival of the right parts and the right data in the right place at the right time to the right quality standard, through the entire value stream” We have about 15 processes including the transversal Manage the Supply chain, and we insured all SCMH chapters covers each processes. Plant, material, skills & capacity planning & Scheduling Plant, material, skills & capacity planning & Scheduling Manufacturing Manufacturing Post Delivery Support and services Post Delivery Support Order Management (internal & external) Order Management (internal & external) Inventory planning & optimization Inventory planning & optimization Logistic Management Logistic Management Non Conformity Management Non Conformity Management
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Example Chapter 1 - Supplier Maturity Assessment
per Supply Chain Process Example Four levels of maturity (Maturity model CMMI like) Undefined : No Process, Method, Tools/ No Process, Method, Tools/ and Appropriate Behaviours Defined Applied Optimising: Implemented and optimised, continuous improvement Four domains assessed: People & Organisation Processes Tools & Data Performances Metrics Non Conformity Non Conformity 1 1 2 2 3 3 4 4 Undefined Undefined Defined Defined Applied Applied Optimizing Optimizing Management Management People & Organization People & Organization No clear Accountability No clear Accountability Expert firefighters Expert firefighters Clear accountability Clear accountability Multifunctional team Multifunctional team No Problem solving No Problem solving Cross functions Cross functions Highly Skilled Highly Skilled skills skills Highly skilled Highly skilled Process Process Reactive needs Reactive needs Ad hoc firefighting Ad hoc firefighting Root cause process in Root cause process in Mature process for root Mature process for root Customer Stimulus Customer Stimulus actions actions place place cause & preventive cause & preventive Process playbooks Process playbooks actions actions Limited preventive actions Limited preventive actions Tools & Data Tools & Data Manual : Fax e Manual : Fax e - - mail mail Multiple Data base Multiple Data base Integrated database, clear Integrated database, clear Internal & external Internal & external Expectation Supplier performance workflows, internal workflows, internal collaboration. collaboration. Spreadsheet Spreadsheet collaboration collaboration Real time intelligent Real time intelligent workflows workflows Performance Performance No measurement of No measurement of Measuring performance Measuring performance Performance drives action Performance drives action 3+ regular review of 3+ regular review of Performance Performance plans plans metrics effectiveness metrics effectiveness Metrics Metrics
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Supplier Assessment Results
Chapter 1 - Decision making process Standard Questionnaire and Assessment results independent from the size of company and product/project criticality… Supplier Assessment Results Decision to select or not based on risk analysis like 9134 “Supply Chain Risk Management guideline” (Special action plan if not capable but need to select) Each Company to apply weighting to each process as appropriate to their Product, Customer, Risks, etc…
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Deliverables by Seville
Chapter 1 : Supplier Selection & Capability Assessment Deliverables by Seville Agree on the definition of the 15 Supply Chain Mgmnt processes Agree on the maturity matrix concept and finalize its content Conduct pilot assessments, using the maturity matrix and model, in all sectors Finalise decision matrix and questionnaire Actions to be completed later Validate questionnaire and Maturity Model during on the pilot phase Publish questionnaire and Maturity Model decision matrices Issue training package Identify Requirements,Guideline and Best Practices Best Practice Sharing: Deliverables that can be shared across the industry to stimulate voluntary improvements in process performance Common processes, to be widely used at all tier levels Guideline or Recommended Practice: This would be a level up from “Best Practice Sharing” and would be more actively promoted to speed up deployment, some companies may insist upon deployment through supply contracts Standard: This would be the top level of three and would be reserved for those items that we feel strongly enough about to mandate deployment through Standards
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Chapter 2: Requirements & Flowdown
Brainstorm of Causes Affinitize Causes Customer Supplier C & S Suppliers Produce Non-conforming Product because they do not understand the requirements or do not receive the requirements. WHY? Customer Supplier C & S Reqts Def Contr. Rev Change Mgt
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2.0 Requirements and Flowdown
Chapter 2.0 Requirements and Flowdown 2.0 Requirements and Flowdown 2.1 How to clearly identify and communicate requirements throughout the supply chain 2.2 How to generate a shared understanding of the requirements 2.3 How to manage revisions to requirements after initial contract/purchase order release
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Chapter 2 - Requirements and Flowdown
Deliverables by Seville: Connect to others doing similar work (Missile Defense Agency, Space Quality Improvement Council) to see if we can combine efforts Communicate our work to others (AIA, ASQ) Collect best practices and white papers from aerospace and other industries Actions to be completed later Benchmark Medical Device Industry and SEA on Requirements & Flowdown Publish guidelines/best practices by June 07
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Product Realization Activities have been tasked Chapters 3, 4 and 7
3.0 New Product Introduction 1.0 Supplier Selection & Capability Assessment 2.0 Requirements and Flowdown 4.0 Process Control 5.0 Product Verification & Acceptance 6.0 Controlling Non-Conf Product 7.0 Work Transfer Management 9.0 On going Approval And Maintenance 8.0 Supply Chain Mgmnt and Performance Measures 10.0 Program Management In work by Product Realization Stream In work by Supply Chain Process Capability Stream
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Chapter 3 – New Product Introduction
No Change From Montreal Background: The Aerospace Industry developed a successful product introduction process based on a 20%-80% outsource ratio and the industry has migrated to a 80%-20% outsource ratio This change was gradual and a change in the product introduction process was not undertaken Corrective Action proposed: Develop a product introduction process that accurately predicts supplier performance at production levels
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Chapter 3 – New Product Introduction
Status: Benchmarking performed: Dell computers Toyota USA Knowles (Medical) Lessons learned and brainstorming have produced Sub-chapters headings Benchmarking for chapter 7.0 results will be used for chapter 3.0 analysis.
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Chapter 3 – New product introduction
3.1 Pre-production Process validation (product specific) 3.2 Review of Quality Planning including Key Characteristics 3.3 Product and Process Qualification 3.4 Pre-approval of test methods (where applicable) 3.5 FAI (9102) 3.6 Design Change Requirements 3.7 Product Maturity Assurance
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Chapter 3 - New product introduction
Deliverables by Seville: Confirm sub-chapters headings, resolve overlaps with other chapters Collect best practices from IAQG and other companies Actions to be completed later Publish guidelines/best practices by June 07
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Chapter 4 - Process Control
No Change From Montreal 9103 (Variation Management of Key Characteristics) not sufficiently and adequately deployed Value not clearly identified or understood All functions to be involved, not only Quality Lack of buy-in Training required Need to explain how to apply 9103 based upon supplier & product complexity Lack of skills
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Chapter 4 - Process Control
Since Montreal, EAQG has worked on 9103 education package: Common part (key concepts with IAQG banner) for all companies using the training Some area to be adapted by each company when training its staff or its suppliers (examples, tools, forms, etc…) Education package content: Will focus on value of doing it and risks and/or costs of not doing it Should take difficulties of doing it into consideration Work is on going
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Chapter 4 - Process Control 9103 deployment Constraints
Application of 9103 should be risk oriented (not used if no added value, should focus on the results, not on the tool or the process) More chance to succeed if convinced of business value than if strict mandate: Improve communication and learn more from supplier experience and constraints 3 ways of flowing 9103 down (deployment drivers) ? Mandated (high risk product and/or existing key characteristics) Guideline Best practices sharing Mandate from customer At supplier own initiative or supplier development Need to create a global culture (prime, suppliers) rather than one way (mandate) => engagement within all levels and functions of the supply chain
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Chapter 4 - Process Control Further Actions
Measure the effectiveness of 9103 deployment and its benefits on the overall business Build on lessons learned See how to define key characteristics Introduce concept of FAI stage 1 (initial) and stage 2 (confirm capability at ramp up) Evaluate how to use 9103 results to optimize design for manufacturing
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Chapter 4 - Process Control Interconnection between several topics
“Global Process Control” brainstorming : We can build from 9103 but shall not limit to it and shall not consider it as the only key factor of success
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Chapter 4 - Process Control
4.1 Variation management of Key Characteristics (9103) 4.2 Root cause analysis and problem Solving 4.3 Process capability and control 4.4 Design for Manufacturing and Relation with Manufacturing Capability 4.5 Process Change Requirements 4.6 Industrial Capability and Capacity Assessment 4.7 First Article Inspection 4.8 Special Process Control
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Chapter 4 - Process Control Proposed Short Term Action plan
Deliverables by Seville: Finalize 9103 education package Be ready for deployment of the 9103 training Actions to be completed later Start to work on Root Cause Analysis and Problem solving Evaluate the effectiveness of 9103 deployment Reviewing opportunity for Process Control improvement based on feedback from deployment (industry expectations) Build on 9103 (evolution of the standard or complementary standards or methodology)
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Chapter 7 – Work Transfer
Supplier A Supplier B Going to talk about whats probably the most visible part of the IAQGs work- its initiatives, particularly the documents it produces You may be aware of the Standards that the IAQG produces but the IAQG also produces Guidelines Many of the initiiatives to produce these documents start off as global activities, others start within one of the IAQG sectors and then move to become world wide documents. Unsuccessful work transfer is a major problem for the industry and we feel it is one of our priorities We have not standardised process to do it
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Chapter 7 – Work Transfer
Collected Industry Best Practices (Benchmarking) Dell computers Toyota USA Knowles (Medical) Standardize Knowledge and Lessons learned Pre-transition Program Planning Pre-production meeting(s) – upfront effort Multidiscipline Team (Agreement: quality, eng., purch.) Capture Hidden Factory – Last Article audit (product and process) Receiving Supplier Process Capability & Assessment Supplier Development – as required Standardize Knowledge back-up – Preproduction Meeting Up front effort w/suppliers, pre-qual, capability Before suppliers receive work Multidiscipline Team (qual, eng, purch.) (Dell) made sure they understood requirements Work instructions were locked out Supplier Development Supplier is accountable for quality and delivery but if they cannot meet expectations then we must assist them before impact. (Dell) development has to happen Supplier Accountability Hidden Factory, last article, tooling, equipment, Technical Data Package Review Agree on Core Requirements Back-up -- Create chapters as guidelines for Work Transfer Management 7.0 and New Product Link to existing/future standards where possible (i.e. First Article 9102, Process Cert. 9103) Team presently focusing on defining the “process”.
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Chapter 7 – Work Transfer
Deliverables in Seville: Confirm sub-chapters headings Identify overlaps, existing/needed standards Collect best practices from IAQG and other companies Actions to be completed later Develop a transition process from best practices, ensuring risks are identified and mitigated prior to the work transfer decision and launch Publish guidelines/best practices by June 07 Agree on Core Requirements Back-up -- Create chapters as guidelines for Work Transfer Management 7.0 and New Product Link to existing/future standards where possible (i.e. First Article 9102, Process Cert. 9103) Team presently focusing on defining the “process”.
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Supply Chain Management Handbook Next steps
Finalize Chapter Headings and Sub Chapter titles and content/objectives to eliminate overlaps, improve clarity and integration (June 06) SAE has provided a “public web space” for our team to communicate with the general public on our progress. We will populate this web space in coordination with the IAQG communications team
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