PSA_供应商质量保证工作方法.ppt

1、,PSA 供应商质量保证工作方法,PSAs Quality Management Procedure PSA 质 量 工 作 步 骤 介 绍,3 Stages: 3个阶段：,Stage 1, Need expressing and supplier choosing. 阶段1，需求的表达和供应商的选择。,Stage 2, Quality Assurance by Product and Process Management (AQMPP in French). 阶段2，通过产品和过程的控制实现质量保证 (简称AQMPP).,Stage3, Quality Control in Mass Pro

2、duction 阶段3，量产阶段生产产品的质量控制.,Supplier Pre-qualification 供应商预鉴定,Objective of Stage 1 第 1 阶 段 的 目 的,To express clearly and precisely the needs of vehicle manufacturer by means of complete and exhaustive consultation documents:plans, standards, technical specifications of design (STE in french), material

3、s, experiments, validation plans,etc 借助于完整齐全的咨询文档资料：图纸，标准， 技术规定（STE），材料，试验，确认计划等来清楚、准确地表达PSA的需求。,Need expressing and supplier choosing 需求的表达和供应商的选择,To retain the most competitive supplier, who can guarantee the required quality level and fulfill the obligations of his offer.选择最具竞争力，最有能力保证达到所要求的质量水平，

4、并能对其报价负责任的供应商。,To formalize the responsibilities. 明文规定各种职责。,Consultation Documents 咨 询 文 件,Management and Quality assurance Clauses 管 理 及 质 量 保 障 条 款,Technical Specification 技 术 规 范,Contractual and economic specifications 合同规定要求的技术说明书,Consultation document 咨 询 文 件,Figure, economic objectives, partne

5、rship,spare parts, guarantee, 数字, 经济目标, 合作关系, 备件, 保修,Requirements and objectives related to products 与产品有关的要求及目标,Requirements to ensure the quality control of all the delivery 确保控制整个供货链质量的相关要求,Management and Quality assurance Clauses 管 理 及 质 量 保 障 条 款,Technical specification 技 术 规 范,Contractual and

6、economic specifications 带有契约条款要求的技术说明书,Consultation documents:responsibility 咨 询 文 件 ： 职 责,For PSA, it helps to precise : Project team organisation of PSA, Disposals for project follow up, Product quality objectives, The respective responsibilities, Disposals for quality assurance, Deviation treatme

7、nts, Audits (Process, Products), and the expected results,对PSA而言，它用于明确： PSA的项目组织， 项目的跟踪措施， 产品的质量目标， 各自的职责， 质量保证措施， 偏差的处理， 审核（过程，产品）， 以及所期待的效果,Management & Quality assurance Clauses 管 理 条 款 与 质 量 条 款,How can this be useful ? 有 何 作 用 ?,Management & Quality assurance Clauses 管 理 条 款 与 质 量 条 款,PROJECT M

8、ANAGEMENT CLAUSES 项目管理条款 Project organization项目组织 General planning stages and scheduling of reviews/计划的一般阶段和评审的定位 PSA team organization / PSA项目组的构成 Supplier team organization /供应商项目组的构成 Sharing of tasks between PSA and the Supplier / PSA和供应商任务的分配 Planning and checking the work工作的计划及控制 Activity Repor

9、t /活动报告 Monitoring the progressive qualification of the product and the process /产品和过程的逐步鉴定跟踪,Management & Quality assurance Clauses 管 理 条 款 与 质 量 条 款,QUALITY ASSURANCE CLAUSES 质量保证条款 Quality objectives and requirements质量目标及要求 Commitment to operational security : Safety /功能确定性承诺：安全性 Commitment relat

10、ing to failure /故障承诺 Commitment relating to reliability /可靠性承诺 Commitment to aptitude for maintenance /可维护性承诺 Commitment to quality as new /新品质量承诺 Quality Assurance Measures质量保证措施 Requirements relating to dealing with known defects (Fault Eradication Plan)/已知缺陷处理要求（缺陷消除计划） Requirements relating to d

11、ealing with risks (Risk Management Plan)/风险处理要求（风险控制计划） Requirements relating to operational safety (Operational Safety Plan)/运行确定性要求（运行确定性计划） n Rank Suppliers /N级供应商 Dealing with technical changes技术处理,The supplier will take his responsibility since his response to consultation 供 应 商 一 旦 投 标 就 意 味 着

12、 其 承 担 责 任,Through his offer, the supplier will take his responsibility to 通过投标，供应商承担如下责任：, To meet the explicit and implicit requirements of the technical specifications, to respect the management and quality assurance clauses 满足技术条件中明示的和隐含的要求并遵守质量管理条款,This is much more than to commit oneself to a

13、price and carrying out the proposed technical solutions. 因此，供应商的责任范围不仅仅是报价并实施所建议的技术方案。,The need expressing has been formalized and optimized.需求的表达已优化和文件化。 The supplier has been selected.供应商已选定。 The resonsibilities between PSA and supplier have been formalizedPSA和供应商职责已以书面形式确定。,Definitive product mee

14、ts each functional specification.产品确定并满足每个功能要求。 Definitive process, adjusted and be able to produce only good parts过程确定, 调试，并有能力只提供合格产品。,AQMPP situation in Quality ProcedureAQMPP 在 质 量 步 骤 中 的 位 置,Product/Process Qualification Steps产 品 / 过 程 鉴 定 步 骤,Stage 1阶 段 1 Need expressing and supplier choosing

15、 需求表达和 供应商选择,Stage 2阶 段 2 Quality Assurance by Product and Process Management 通 过 产 品 和 过 程 控 制 保 证 质 量,Stage 3阶 段 3 Quality Control in Mass Production 批量产品质量控制,Preliminary Technical Analysis(ATP)技 术 预 分 析,AQMPP Initialization Review AQMPP 初 始 化 评 审,Sequence of this step 本 阶 段 的 展 开,Confrontation &

16、communication and Convergence 对照交流并达成协议,To be prepared for AQMPP initialization review, PSA and Supplier make a list from each side of all worries to be taken into consideration, so as to work out Q3P (Qualification Progressive of Product and Process) steps. 供应商和PSA各自汇总所有需要考虑的任务细节，为AQMPP初始化评审会议作准备，目

17、的在于建立产品及过程逐步鉴定(简称Q3P)的工作方法。,Preliminary Technical Analysis(ATP)技 术 预 分 析 ( 简 称 ATP ),Why? 为什么？,Suppliers Preliminary Technical Analysis 供 应 商 技 术 预 分 析,Identification of the tasks and the proposition of task-sharing between PSA and supplier 识别出工作任务、PSA/供应商之间的分工 Identification of risks about product

18、and process识别出产品和过程的风险因素 Steps for defects eradication缺陷消除工作步骤 Development plan开发计划 Product validation plan 产品认可计划 Function reliability plan运行确定性计划 Process description 对过程进行描述 Components and materials origin配件及材料来源 Industrial diagram, industrialization plan 工业简图，工业化计划：即平面布局图和新设备新流水线的设置 Quality plan,

19、 quality commitments质量计划，质量承诺 Logistic means 物流设备 Identification of project members项目组成员识别,Letter type Suppliers ATP 供应商技术预分析标准信件,The supplier sets up a scaffolding to build up the quality of product and process供 应 商 搭 建 “ 脚 手 架 ” 以 架 构 起 产 品 和 过 程 的 质 量,Parts definition, references, parts index and

20、 project planning 零件定义，编号，零件及图纸更改标记，项目计划 Responsibilities sharing between PSA/supplierPSA/供应商之间的职责分工 Quality risks and recordings 质量风险及历史纪录 Steps of defects eradication缺陷消除工作步骤 Essential Functional and Technical Characteristics关键技术与功能特性（简称CTFE） Identification of projects members 项目组成员识别 Logistics, l

21、ogistic means, and investment物流，物流设备，设备投资,PSA Prelimininary Technical Analysis PSA 技 术 预 分 析,SummaryPSAs ATP PSA的技术预分析总结,Initialisation Review（1/2） 初 始 化 评 审 （1/2）,To formalize the definitions, references, logistics, project planning 将零件定义，编号，物流，项目计划编制成文 To formalize the responsibilities sharing bet

22、ween PSA and supplier 将PSA/供应商之间的职责分工形成文本 To formalize the major risks of the project, precise the milestone of control plan 将项目的主要风险形成文本, 明确监控计划的立标检查制度 To carry out risks control and defects eradification steps 实施缺陷消除及风险控制工作步骤 To precise the Essential Functional and Technical Characteristics 明确关键技术

23、和功能特性（简称CTFE）,Initialisation Review（2/2） 初 始 化 评 审 （2/2）,To formalize the product validation plan (material, test, function, reliability) 将产品认可计划编成文本（材料，试验，功能，可靠性等。） To formalize the development and industrialization plan 将开发及工业化计划编成文本 To make the milestone for product and process validation 对产品和过程认

24、可的重要节点 To work out the interactive questionnaire 实施互动式问卷 To ratify the quality plan and quality objectives 批准质量计划及质量目标 To initialize Q3P form (Qualification Progressive of Product and Process) 产品及过程逐步审核表格（简称Q3P表格）初始化,Initialisation Report 初始化会议报告,Initialisation Review 初 始 化 评 审,Participants 成员,Suppl

25、ier : project team ( at least the team leader, technical pilot, quality pilot) 供应商方面：项目组（至少包括项目主管，技术主管及质量负责人） PSA: PPP: Pilot Product and Process or representative expert 行业产品过程主管 (PPP) 或行业代表人 AAQO: Animator Quality Assurance Operational 质量保证实施推进人 (AAQO) Auditor from Shanghai office上海采购办事处的审核员 Proje

26、ct Buyer (AP) or sourcing officer from Shanghai office项目采购员 (AP) 或上海采购办事处的采购员,Initialisation Review初 始 化 评 审,To enrich his technology with his experience 把经验反馈纳入其专业领域 To propose the industrial solutions, quality plan, industrialisation plan, development plan and action plans 建议并说明工业化技术方案，质量计划，工业化和开发

27、计划，行动计划 To explain his understanding of PSAs requirements: CTFE, planning, CMQ, quality requirements 阐述如何认真对待PSA的要求: 关键技术和功能特性（ CTFE）, 计划，管理及质量条款（简称CMQ）, 质量要求 To justify his choice and provide documents 对自己选择的全部方案进行论证并文件化,ROLE of Supplier 供应商的角色,Initialisation Review初 始 化 评 审,To officialize product

28、requirements of PSA (general plan, specification sheet, technique specifications, standard, validation plan, testing sharing) 正式化PSA的产品要求（底图，技术任务书，技术规范，标准，认可计划，试验分工） To validate the suppliers proposals: Process description, development or industrialisation plan, defects eradication plan, material ch

29、oices ,origins of components 对供应商的提议进行生效：过程描述，开发和工业化计划，缺陷消除计划，材料选择，组件来源等进行确认 To be in charge of guiding the development (for co-development parts ) 将负责项目开发的推进（对共同开发的零件而言）,ROLE PPP 行业产品过程主管的角色,Initialisation Review初 始 化 评 审,Working under the responsibility of technical experts 在行业专家的领导下开展工作 Having wr

30、itten the Management and Quality assurance Clauses ( CMQ), and contents of PSAs ATP. (Preliminary Technical Analysis) 已编制管理与质量条款（CMQ）及PSA技术预分析内容 Having gathered the list of risks identified by the differents interlocutors PSA, and make sure the distribution.已收集由PSA各方面参与者识别的风险，编制了清单并确保发放 Making sure

31、the suppliers proposals correspond with CMQ requirements. 确保供应商的建议符合质量管理条款的要求,ROLE AAQO 质量保证实施组织者的任务,Initialisation Review初 始 化 评 审,To guide the Initialization Review and the project follow up meetings, and write the minutes. 主持初始化评审及项目复审会议，撰写以后会议纪要。 To ensure the agreements between the supplier and

32、 PSA , concerning the industrialisation plans, communication plan, and quality plan 确保供应商和PSA就工业化计划, 交流计划, 质量计划.达成协议。 During the whole development, be responsible to ensure the fulfilling of suppliers commitments: parts prices, investment, planning, parts delivery, parts traceability. 在整个开发过程中将负责监督供

33、应商承诺的遵守：零件价格, 投资, 计划，零件发送，检验报告，零件可追溯性。,ROLE Project Buyer (AP) 项目采购员角色,Product/Process Qualification Steps 产 品 / 过 程 鉴 定 步 骤,Stage 1 阶段1 Need expressing and supplier choosing 需求表达和 供应商选择,Stage 2 阶段2 Quality Assurance by Product and Process Management 通过产品和过程控制保证质量,Stage 3 阶段3 Quality Control in Mass

34、 Production 批量产品质量控制,Second part: Q3P form 第二部分: Q3P 表格,Second Part:Q3P Form第 二 部 分 ：Q3P 表 格,Q3P, whats this?什么是Q3P？,QPPP：Qualification Progressive of Product and Process （Q3P）QPPP: 对产品和过程的逐步鉴定,One common methodology to qualify gradually the product and the process. 是一个逐步鉴定产品和过程的通用方法。,Several steps

35、: Q3P qualification steps which pass from one to another. 分几个阶段：由Q3P的鉴定状态实现从一个阶段到另一个阶段的过渡。,Some timing follow-up indicators of product and process development. 包括对产品及过程开发进程跟踪的一系列指标。,Second Part:Q3P Form第 二 部 分 ：Q3P 表 格,Q3P Form : principle Q3P 表 格 ：原 理,Q3P Requirements Q3P要求,Delivery qualified and i

36、n time 按时并且合格的交付,Delivery non-qualified or seriously delayed 不合格或严重延迟交付,Delayed and/or the delivery quality inacceptable 延迟交付不可接受和/或交付质量不可接受,Once one deviation happens :一旦发现偏差： Implement action plans (AAQO/Supplier) 实施行动计划（质量保证实施推进人 / 供应商） If necessary, intervention to the supplier (Project team) 如有

37、必要，介入供应商 （由项目组）,Q3P : signification of coulours Q3P 中 颜 色 的 含 义,DFE (Distribution design) : Product designDFE （产品设计发放）： 产品设计阶段 SRU (Unique representative stage) : Prototype validationSRU （唯一代表性阶段）： 样品确认阶段 OCM (Officialisation of Creations or Modifications) : Definition officializationOCM （创立或修改正式化）：

38、 定义正式化阶段 IOD (Made by definitive tools) : Making representative partsIOD （源自最终工装）： 代表性零件的生产阶段 PRSHL (Try-production out line) : Making cars with non-definitive processPRSHL （线外预批）： 过程未经确认的车辆生产阶段 PRSEL (Try-production on line) : Making cars with definitive processPRSEL （线上预批）： 过程得到最终确认的车辆生产阶段 AVS ML

39、(Before mass production batch method) : Making marketable cars by batchAVS ML （批量前批接收）： 按批次商品化车辆生产阶段 MEC (Raise production) : Making marketable cars in mass productionMEC （发展满负荷生产）： 商品化批量生产阶段,Differents Q3P Steps definition Q3P 各 阶 段,For reference指示性 (For vehicle project) （对某整车项目而言）,J7 +24s,The diff

40、erent steps of Q3P Q3P 各 阶 段, Product definition control 产品定义控制 Product validation control 产品认可控制 Control of operating relibility, risks and defects 运行确定性，风险及缺陷控制 Control of CTFEs (Essential Functional and Technical Characteristics) 关键技术和功能特性（ 简称 CTFE）控制 Control of product compliance 产品合格性控制 Product

41、 qualification summary package 产品审核的综合资料,Q3P : Items for Product Progressive Qualification Q3P 中 产 品 逐 步 审 核 项 目,Q3P : Items of Process Progressive Qualification Q3P 中 过 程 逐 步 审 核 项 目, Control of process scheduling, tracking and risks 计划、可追溯性及过程风险的控制 Control of process definition and industrialisati

42、on 过程定义的控制及工业化控制 Control of grade 2 and above suppliers 2级及以上供应商控制 Control of packing and logistics 物流和包装的控制 Process qualification summary package 过程审核的综合资料,Q3P FormQ3P 表 格,SUPPORT Q3PQ3P载体,Q3P filling in each step Q3P 表 格 各 阶 段 填 写,http:b2b.psa-peugeot-,Step SRU SRU阶段,Step OCM OCM阶段,Q3P validation

43、step by stepQ3P 各 阶 段 逐 一 认 可,Macro Procedure Q3P 宏 观 Q3P 过 程,Steps Requirements of Product and Process Qualification in Q3PQ3P 表 格 中 产 品 和 过 程 鉴 定 的 不 同 阶 段 的 要 求,Q3P : Product acceptance state requirements (supply by batch) Q3P: 产 品 验 收 状 态 的 要 求（产品批次供货）,Q3P follow-up requirements (product / proce

44、ss) Q3P要求的跟踪（产品/过程）,2 Lettres + 1 Number 两个字母 + 一个数字,Q3P : Product Acceptance State Q3P: 产 品 验 收 状 态,Q3P : Acceptance State of Expected Product Q3P: 所 期 待 的 产 品 验 收 状 态（可接受的下限）,ATTENTION THE SUPPLIER DOES THE QUALIFICATION,AND THE QUALIFICATION IS ACCEPTED BY PSA,BUT注意供应商做了鉴定，并且鉴定被PSA所接受，但是 ,Accept

45、the results of suppliers product and process qualification does not mean under any circumastances the responsibility transfered from supplier to PSA ! 对供应商提交的产品及过程鉴定结果的认可并不意味着供应商对PSA责任的转移！,Q3P: a follow-up and an alert form, with all supporting documents required Q3P 基于要求提交的各类文件，, be completed throu

46、gh some different interventions, timing follow-up, audit, validation, action plans follow-up 并辅助于通过诸如进展跟踪，审核，验收，对改进计划进行跟踪等方式来参与进来的一种跟踪和报警的表格。,Q3P, a formand some interventions PSA Q3P 表 格 及 PSA 的 介 入,Pilot 主导人： Project manager 项目负责人 Organizer 组织人： Buyer 采购员,Executors 实施人： several actors 多个参与者： Audit

47、or, project team,buyer,expert审核员，项目小组，采购员，专家,The interventions frequence varies according to the risks and trust level 介入的频次根据风险程度及信任度而不同,Q3P, a formand some interventions PSA Q3P 表 格 及 PSA 的 介 入,Q3P, a formand some interventions PSAQ3P 表 格 及 PSA 的 介 入,Some different interventions PSA: Timing follow

48、-up meeting Product/Process Review Development Audit Action plans follow-up Product/Process acceptance visit Full rate production evaluation Product conformity checking Etc,PSA 各 种 介 入 方 式 ： 进展跟踪会议 产品/过程评审 开发审核 行动计划跟踪 产品/过程验审参观 满负荷生产能力评估 核实产品合格性 等等 ,Objective 目标,Who? 谁？,Verify deeply that the proced

49、ure of offer preparation, project management, product and process development are strictly respected. 通过深入分析，检验报价、项目管理、产品开发及过程开发等程序是否得到了严格的遵守。,How? 怎样？,When? 何时?,By the application of right audit form evaluating the suppliers function and situation, and the risks in different steps. 通过使用相应的质量审核表格，评估

50、供应商运作的实际情况和各个阶段的风险。,One qualified auditor accompanied by a buyer and/or an expert.由授权了的质量审核员来实施，必要时，采购员和/或专家进行参与,By the request of PSA project team 应PSA项目小组要求 By the request of buyer 应采购员要求,Development Audit开 发 审 核,Objective 目标,How? 怎样？,Who? 谁？,Product/Process acceptance visit 产品/过程验证的参观,Q3P, a form

51、and some interventions PSAQ3P 表 格 及 PSA 的 介 入,Verify the expected intermediate results about product and process 验证产品和过程所期望的中间阶段的效果,By scheduled visit 根据计划好的参观频次。,Carried out by project team, one auditor, and some technical experts if necessary. 由项目组，审核员及技术专家来进行，必要时，工艺人员参与,When? 何时？,At the end of Q3

52、P review Q3P评审结束后 Until the cloture of form 直到表格填写完整 Security approval (if security parts) 安全协议签定（如是安全件） Others 其它要求,Q3P, a formand some interventions PSAQ3P表格 及PSA的介入,Product/process acceptance visit 产品/过程验收的参观,Objective目标,To be sure that all the production means are ready确保所有的设施安装就位 To estimate th

53、e capacity of production means 评估生产设备的能力 To evaluate the ability of the supplier to guarantee the quality/quantity of mass production supplying评估供应商批量生产阶段保质保量交付货物的能力 To verify the conditions to get the potential of saturation验证潜在饱和的获得条件,Full Rate Production Evaluation 满 产 评 估,How? 如何？,Who? 由谁？,Full

54、Rate Production Evaluation满 产 评 估,Potentiel nominal 潜在产能,When? 何时？,EPC 1 : during PRS EL1 满产评估1： 线上预批1阶段 EPC 2 : before PSA raise production 满产评估2： PSA批量增长之前,Full Rate Production Evaluation 满 产 评 估,The product has been qualified by the supplier, 产品已由供应商自己鉴定完毕，,.So, all that could be anticipated has

55、been carried out in a preventive manner.And now, this must be confirmed as efficient and pertinent under mass production conditions 这样，所有作为预防而事先考虑好的措施都已实施。现在必须确认在批量环境下，它是有效的和适宜的.e,Confirmation qualification state at the beginning of mass production 批量生产初期对鉴定状态的确认,This is the subject of the qualifica

56、tion confirmation at the begining of mass production它将作为批量生产初期鉴定状态的确认对象。,The process has been qualified by the supplier, 过程已由供应商自己鉴定完毕，,The results has been accepted by PSA PSA已接受了这些鉴定结果,Carry out the anticipated control plans by the supplier 供应商实施规定的控制计划,In waiting for the efficiency, supervised by

57、 PSA or one institution agreed by PSA: 在等待有效性证实前，PSA或者PSA认可的机构对供应商进行监控 Good verification of CTFE on the products 仔细检查了客户制定产品的关键特性（CTFE ） Good application of control plans 认真实施了规定的控制计划 Good implementation of required packaging and identification 严格执行了要求的包装和标识,Qualification State Confirmation 鉴 定 状 态 的 确 认,Qualification State Confirmation 鉴 定 状 态 的 确 认,4 levels of surpervision are forecasted according to suppliers risks and products risks : 根据供应商和产品的风险程度进行4个层次的监控： - simple audit after 1 month of mass prod