物料评审程序中英文版教程文件
物料评审程序中英文版
______________________________________________________________________________________________________ For m N o.表格編號﹕BZQP -4-01F01.3PURPOSE目的:To establish a procedure for reviewing and disposing non-conforming materials,semi-product,finished products andRMA control in Beckett(ZhongShan).本程序规定对来料检验及生产过程中发现的不合格物料,半成品,成品及客户退回品的评审及处置方法.2.SCOPE范围:This procedure is only applicable toXXXX(ZhongShan).本程序适用于XXX(中山)公司.3.DEFINITIONS定义:3.1PRD:Product Department生產部3.2ME:Manufacture Engineering制造工程3.3RTV:Return To Vendor/Supplier退回供應商3.4UAI:Use As It Is讓步接受3.5SORT:Segregation Of Bad And Good Unit選用3.6SCAR Supplier/Sub-contractor Corrective Action Request(8D)供應商改進行動要求(8D)3.7GRN:Goods Receipt Note收货单3.8MRR:Material Review Record物料评审记录4.REFERENCE DOCUMENT参考文件:4.1BZQP-7-05Raw Material Quality Control Procedure原材料质量控制程序4.2BZQP-8-05Nonconforming Control Procedure不合格品控制程序4.3BZQP-8-06Stop Shipment and Purge Order Procedure停止出貨和清除指令程序.4.4BZQP-8-07Corrective and Preventive Actions Procedure纠正及预防措施程序.5.RESPONSIBILITY职责:5.1QA is responsible to chair MRB meeting when defective material are defected in line,QA review the non-conformingproducts and issue SCAR(8D)if necessary.当不合格物料在产线发现时,QA负责主持MRB会议,确认不合格产品,并在必要的情况下发出Form No.表格編號﹕BZQP-4-01F01.3SCAR(8D).5.2PRD is responsible to fill MRB label and inform QA members to review the non-conforming products,andreturn them to warehouse.生产部负责填写MRB标签并通知品质部成员评审不合格品,并将不合格品退回货仓.5.3PUR/IQC are responsible to inform supplier of the non-conforming data,PUR responsible to arrange the non-conforming materials RTV.采购/IQC负责将不合格批物料状况通告客户或供货商,采购还负责安排将不合格品退回供货商.5.4PUR is responsible to charge the supplier of sorting/reworking cost and other loss due to material quality issue,and call MRB meeting to review the reject lots of IQC raised.采购负责向供货商索取选用或重工费用及由于物料问题而导致的损失,并召集MRB会议处理IQC拒收的紧急物料.5.5ME is responsible to analyze non-conforming products.ME负责分析不合格品.5.6All MRB members are to propose and decide on defective material disposition and carry out the follow-upactions as agreed in the meeting.所有MRB成员负责执行MRB会议之决议,并跟进MRB会议决定的所有行动措施.5.7IQC is responsible to confirmed material which is suspected has defect.And IQC drive supplier to takecorrective action if necessary.IQC负责对被怀疑的物料进行确认,并且在必要的情况下,将要求供货商对其进行改善.6.PROCEDURE程序:6.1MRB team consist MRB小组成员Normally,MRB team consists QA,PRD,PMC,PUR managers or whose dictated representative,if necessary other related members also can attend the meeting(such as supplier,customer etc.).通常,MRB小组由品质部、生产部、物料部、采购的部门经理或其指定代表组成,如有必要其它相关的成员也应参加(例如供货商,客户等).6.2Incoming Inspection Reject來料檢驗不合格6.2.1When the incoming lot is rejected by Beckett(ZhongShan),IQC for quality or other causes,it shouldbe marked on the GRN sheet.当来料检验批判定不合格后,由IQC注明于收货单.6.2.2The rejected lot will be put into IQC Reject area by WH.If the coverage of defects is beyond IQC area,IQC shall work with QA to consider raising a purge order.不合格物料由货仓转移至IQC拒收区隔离存放,如果不合格不仅仅发生在IQC,IQC需会同QA 发出清除指令.6.2.3IQC fill in MRB form to QA manager and related departments for reviewing the rejected lot,the resultmaybe as below:IQC开出MRB单给品质经理及相关部门对不合格物料进行评审,处理结果有如下几类:6.2.3.1RTV:Per PUR confirm,the rejected lot can be returned to supplier,this decision should bemade,the MRB decision should be noted on the MRB form,it must be approved by the QAmanager or whose representative at least.RTV:经采购确认,如果不良批可退返供货商,应做出RTV的决定,此决定需注明于MRB单上,且至少由QA经理或其指定代表签署.6.2.3.2UAI:Use as it is.If the material lot is very urgent to the production and according to theevaluation of MRB members,the defect/nonconformity will not lead impact/defect to ourfinished product quality,the decision of UAI may be made and recorded on the MRR sheet,itneed be approved by the QA manager,ME,and PUR.or whose representatives of otherdepartment,it needs Production manager’s approval if necessary.QA and ME should monitorthe effect of UAI material using.Note:if the defect maybe cause finished products quality issue,it must be promised by ourcustomer first,then can be made the UAI decision.UAI:让步接受.如果该物料为生产线急需并根据MRB成员的评估不会对成品质量产生影响,则可做让步接受,MRB评判结果记录在MRR单上,且至少有QA经理,采购和工程部或其部门经理的指定代表签署,必要时需生产经理签署。
物料管理程序英文版
6.4 outbound control
6.4.1 for the finished products, semi-finished products or direct delivery parts, take the material requisition or delivery note as the delivery basis to enter the warehouse and enter the account.
A. The storage place must be equipped with fire-fighting equipment and hygrometer.
B. Temperature and humidity meter must be set in the storage place to record the temperature and humidity of the warehouse, and the temperature shall be kept between - 4 ℃ and 40 ℃,keep the humidity between 35% and 75%. Carry out spot check on the temperature and humidity every day and record it in the temperature and humidity spot check table.
中英文进料检验指导书
编制部门:质量部Written Dept.Quality Dept. 发布日期:Issue Date实施日期:Implementation Date1. 目的:Purpose规范IQC进料检验操作,确保外购或外协件品质符合规定要求。
The instruction specifies IQC inspection handle ensure the quality of the purchase and outsourcing part conform to specified requirement2. 适用范围:Scope本指导书适用于本公司机床装配的所有采购件及外协件。
The instruction is mandatory for all purchase and outsourcing part in EMAG Jintan3. 职责: Responsibility3.1 仓库—负责物料的点收,搬运,标识,储存。
Warehouse—responsible for material acception, flitting, identification and storage.3.2 进料检验—负责物料的品质检验/记录。
IQC—responsible for material inspection and record。
3.3 采购—负责将不合格物料信息反馈供应商。
Purchase —responsible for provide NOK material4. 定义definition严重缺陷A Critical defect A 产品存在对使用者的人身及财产安全构成威胁的缺陷,不符合国家法律,法规,可靠性验证等Products pose no threat to the user's personal and property safety of defects, conformity with the national laws, regulations, and reliability test, etc主要缺陷B Major defect B 1.功能及型号缺陷影响正常使用The function and type defects affect the normal use2.尺寸缺陷影响安装或机加工The dimension defects affect installation or machining3.材料缺陷影响工件力学性能The material defects affect the mechanical properties4.结构和外观存在客户难以接受缺陷The structure and appearance defects cannot accept5.无产品标识、无合格证明的物料No product identification,conformity certificate parts轻微缺陷C Minor defect C 上述缺陷以外不影响产品使用和功能的缺陷The other defects do not affect the product assemble and function5. 内容及流程:Content and Process5.1 收货Receipt仓管员需根据供应商提供的《送货单》或《采购合同》核实来料信息,如不符合,将退还供应商;如符合,则将需要检验的放入来料待检区,无需检验的直接入库。
IQC检验程序(中英文)
IQC检验程序IQC Inspection procedure(ISO9001:2015)1.目的Purpose﹕此程序是为了在IQC来料检验过程中作出规范的工作,使投入生产的物料能满足规定的质量标准而制定。
This procedure for IQC normative inspection incoming material, the materials can settle for prescriptive quality standard.2.范围Scope﹕适用于品质部。
Apply to the quality department IQC3.职责responsibility ﹕3.1IQC检验员负责物料的抽样﹐检查﹐提交相关记录和报告及问题样板。
IQC inspector with responsibility for sample, Inspection, Submit related record & report and problem sample.3.2质量组长负责IQC分配检验员工作﹐检验数据以及不合格物料的跟进和处理。
Quality leader with responsibility for distribution IQC inspector work﹐Inspection information & nonconformity material follow and handling3.3质量科文﹐工程师负责不合格品的处理与督遵IQC按此程序进行工作. Quality Engineer & foreman with responsibility for reject material handling.Conduct IQC inspection woke.3.4质量经理对有争议的问题进行最后仲裁.Quality manager arbitration for as having dispute problem.3.5物料组负责物料的验收和保存工作。
某公司程序文件中英对照
company on the relevant articles. 6.2 办公用品及机零配件的采购 Purchase of office article and machine accessory
编号 (No.) QP-采-001 版本 (Edition) A版
发行日期 (Issuing date) 2002/0/26 生效日期 (Effective date) 2002/09/28 页 次 (Page) 3/7页 (3 of 7 pages)
with appropriate quality and quantity. 2.0 范围:公司所有生产物料及机零配件的采购作业均适用本程序。
Scope: This procedure is applicable for the purchase operation of all the production materials and machine accessories
采购作业程序
Purchase Procedure
l inventory status and relevant requirement, making the material purchase requisition demand. For Livatech, the customer will place the order directly, and then submit to the Purchase Dept. for purchase. 6.1.2 采购部接到《本地月度部品纳期管理表》后,选择合格供应商。合格供应商的选择按本程序6.3相关条 款的要求执行。 After receiving the "Local monthly parts leadtime management form", the Purchaing Dept. will select qualified supplier. The qualified supplier selection will be as per relevant requirement of 6.3 in this procedure. 6.1.3 所有采购作业的合格供应商均应来自《合格供应商名录》中(新认定尚未登录的供应商除外)。 All the qualified suppliers for the purchase operation must come from the "List of qualified suppliers" (except for the newly approved but not yet registered suppliers). 6.1.4 采购人员依请购物料的品名、规格、数量及交货期、质量要求等向能满足采购要求的合格供应商以适 当的联络方式询示报价和结算方式,并根据联络结果制作《采购单》。 The purchase personnel shall inquire the quotation and settlement method with appropriate contacting method to
中英文管理评审程序文件
适用于质量和Green Partner管理体系所有部分.
Apply to the entire sections of quality andGreen Partnermanagement system.
3.0定义Definitions:
3.1管理評審management review:由最高管理者就方針和目標,對質量和环境體系的現狀和适應性進行正式的評價。.Formal evaluation by top management of the status and adequacy of the quality and environment system in relation to quality and environment policy and objectives.
ADMMgr:_____________________________
MIS Mgr:_____________________________
Tooling Repair & Maintenance Mgr:
____________________________________
APP
[x]
Signature /Date
5.5.6上次管理評審跟进情况;The follow-up result of the last management review.
5.5.7在质量管理体系和GP管理体系运作过程中,糾正和預防措施的状况及有效性评价;The status and effectiveness assessment of corrective and preventive actions during implementing quality management system,andGP management system.
供应商管理程序(中英文)
供应商管理程序Supplier Management Procedure(IATF16949-2016)1. 目的 Objective规范供应商管理流程,通过各级考核,评选出符合公司要求的原材料供应商,保障公司供应链的持续提升。
To regulate the supplier management process, choose the raw material suppliers that meet our company’s requirements through the reviews t o ensure the supply chain’s improvement.2. 适用范围 Applicable Scope适用于为本公司提供原材料、辅材料的供应商。
Be applied to the suppliers who supply raw materials and auxiliary materials for our company.3. 职责 Responsibilities3.1. 采购部:开发新材料、新技术、新工艺等对产品品质、成本有优势的供应商;依据公司产品的发展趋势及研发进度,导入符合要求供应商;合格供应商的管理。
Purchasing department: develop suppliers who supply new materials, newtechnology and so on and have advantages in product quality and costs. Import the suppliers who can meet the requirements based on our company product development trend and R&D progress; manage the qualified suppliers.3.2.品质部:主导供应商的审核;供应商品质考核及供应商品质管理。
FMEA程序中英文版本
踪措施的实施。
3.2 The Cross Function Team participate in FMEA design, and the plan, formulation and the audit of the process FMEA.
本程序适用于设计和过程FMEA分析活动。
3、Responsibility/职责
3.1 The principal of the design project convene members of relevant departments to form a Cross Function Team to plan, formulate, audit and track the implementation of the measures of FMEA.
设计要求而采用的一种分析技术。
4.4Cross Function Team: a team including personnel of design, process, manufacture, quality, material, sale and some related members, formed with the purpose of planning and evaluating the quality of new product, production facilities, technique equipment, production process flow and process.
3.2多方论证小组参与设计FMEA和过程FMEA的策划、编制和评审。
3.4 The responsible department is responsible for the implementation of the measures.
采购程序(中英文含流程图)
采购程序(中英⽂含流程图)采购程序PURCHASING PROCEDURE采购程序PURCHASING PROCEDURE1. Purpose⽬的Provide a consistent method for assuring purchased material meet XXXX and customer requirements and optimize purchasing cost and efficiency.为了确保所采购的物料满⾜xxxx公司及客户的需要,优化采购成本及效率。
2. Scope范围Apply to all direct and indirect material used for finish goods and non-production material.所有⽤于成品或⽣产当中的直接或间接物料。
3. Reference Document参考⽂件4.1 Purchasing control flow chart (Direct Material) OP-PU-FC-01采购控制流程图(直接物料)4.2 Purchasing control flow chart (Indirect Material) OP-PU-FC-02采购控制流程图(间接物料)4.3 RTV control flow chart OP-PU-FC-03退货流程图4.4 Approval Vendor List (Direct Material) OP-PU-FO-01合格供应商清单4.5 Lead Time Summary (Direct Material) OP-PU-FO-02交货周期汇总4.6 Sorting Cost monthly report OP-PU-FO-05挑选费⽤⽉报表4.7 Purchase Request OP-MC-FO-03采购申请表5. Definition定义5.1 MPS - Master Production Schedule主⽣产计划5.2 MRB – Material Review Board物料评审会5.3 MRP – Material Request Plan物料需求计划5.4 PO - Purchase Order采购单5.5 PR - Purchase Request采购申请表6. General procedure⼀般程序6.1 Responsibilities 责任⼈6.1.1 Buyer is responsible for creating PO, issuing PO to supplier and following up delivery.采购员负责下订单,分发订单及跟踪交期。
ISO9001-2015物料免检程序(中英文)
物料免检程序Material STS Procedure(ISO9001:2015)1.Purpose 目的Establish this procedure to define the qualification criteria of STS material, to define the operation procedure for STS materials, to enhance IQC work efficiency of inspection.Note: This procedure can’t as the supplier’s excuse who wants to relax or exempt the quality liability for their products.建立免检物料的评价标准,规范免检物料的操作流程,提高IQC的检验效率。
注:本程序的建立和执行旨在提高IQC的检验效率,鼓励供应商持续高品质的为我司供货,但并不作为供应商对其产品质量责任豁免的依据。
2.Scope 适用范围This procedure applied for all production materials which in mass purchasing stage, but not include critical part, subcontract part, customer’s part or customer have special request.适用于本公司量产采购阶段所有的生产性物料,但关键元器件、外协加工件、客供料或客户有特别要求的物料除外。
3.Definition 定义3.1 STS Ship To Store / 直接入仓,即物料免检3.2 RDS Request of Disqualify STS / 物料免检资格取消申请4.Responsibility 职责SQE 供应商品质工程师Drive supplier to improve the quality performance to get STS certification for their product;推动供应商进行品质改善,以促其产品达到STS状态;Review the <STS Material Application List>;《STS物料评审表》的复审;IQE 来料品质工程师Prepare and update the <STS Material Application List>, and submit to SQE to review and submit to quality manager for approval;制备和更新《STS物料评审表》,提交SQE复审以及品质经理批准;Release RDS, to disqualify the STS material;发出RDS,以取消物料的STS资格;Update ERP system data about the material inspection type;更新ERP系统物料检验模式信息;IQC 进料检验组Inspect and mark the STS materials base on ERP system information; 根据ERP系统信息检验和标识STS物料5.Procedure 工作程序5.1 The qualification criteria of STS material / STS物料评定标准The materials may apply to STS if all conditions in below are achieved: 符合下述全部条件的物料,可以申请成为STS物料:a.Continual pass 10 lots by IQC, without any abnormal case or reject; 连续10批IQC检验无异常、无退货;b.The material DPPM in process under the control limit last for 3 month: 在我司生产制程中,该物料连续三个月DPPM达成下述指标:Electrical part and active optical part / 电子物料及有源光器件:100DPPM Mechanical part / 结构件:500DPPMPassive optical part / 无源光器件:500DPPMPCB / 印刷电路板:500DPPMPacking materials / 包材:1000DPPMComments / 注:The total incoming qty and consumed qty should more than 30kpcs.来料总数量和我司使用的总数量须在30K以上。
仓库管理工作流程(中英文版)
部门填写出库单(品名、数量、规格) the departments fill in the list for out of store (the name、specification、quantity)
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部门领班及经理签字领料 the supervisor and the manager sign on the list to get materials
↓Hale Waihona Puke 仓库负责人签字 the storekeeper signs
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发货员签字发货 deliver goods after the sign affixed by the deliverer
填写物料单(日期、品名、规格、数量 、原因) fill in the material list (the date、the name 、specification、quantity and the reason)
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申请部门填写签字 the applying departments fill in and sign
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财务经理审核签字 the finance manager checks and signs
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总经理审批签字 the general manager checks and signs
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交于仓库销账 deliver it to the store to cancel the data
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登记仓库台卡 register the card which is as to the place
5.退货程序: the procedure of returning the goods:
供应商管理程序《中英文版》
1.PURPOSE 目的:To establish a guideline to control and monitor supplier quality performance, manage supplier to improve quality system and product quality to meet XXX (ZhongShan) expectations.建立监控供货商质量绩效的方针,管理供货商改进质量系统及产品质量以达到乂乂乂(中山)的期望目标.2.SCOPE 范围:2.1This procedure applies to all suppliers that provides production material products to XXX (ZhongShan).此程序适合于XXX(中山)提供生产性物料的所有供货商.2.2This procedure is applicable for QA to manage supplier quality and related issue only.此文件仅适用于QA管理供货商质量及相关问题.3.DEFINITIONS 定义:3.1Key Sup plier :The supplier provides the material that is either valuable and / or critical impact to product’s characteristics关键供货商:提供对产品价值或性能有关键影响物料的供货商.3.2SRS: Supplier Rating System.SRS:供货商评估系统.3.3FAI: First Article Inspection.FAI:首件检验.3.4LAR: Lot Accept Rate from incoming inspection.LAR:来料检查批接收率.4.REFERENCE DOCUMENT 参考文件:4.1BZQP-7-06 Supplier Rating System Procedure 供货商评估系统程序.4.2BZQP-8-07 Corrective and preventive actions procedure 纠正及预防措施程序.5.RESPONSIBILITY 职责:5.1Purchasing staff 采购5.1.1Arrange consolidation of the overall material supplier performance and distribute to related parties. 整理供货商质量绩效并发布给相关部门5.1.2Review the supplier performance and enhance supplier improvement management.评估供货商绩效加强供货商改善管理.5.1.3Coordinate and plan supplier’s support both for ongoing & future if necessary.协调和规划供货商现在及将来的支持5.2QA质量工程师.5.2.1Follow supplier corrective action in line complaint.跟进产线投诉问题和供货商的改善行动.5.2.2Define key supplier for evaluation or assessment with purchasing staff.与采购定义关键供货商以便评估.5.2.3Review the assessment result for further improvement or supplier quality related matters..审核供货商质量相关的事项的评估结果,达到持续改善.5.3ME制造工程If necessary, ME will support QA to perform supplier process audit and technology evaluation.必要时,ME将协助QA执行供货商制程审核及技术评估.6.PROCEDURE 程序:6.1Supplier Rating System 供货商级别评估体系.Purchasing and QA shall select the key supplier and perform SRS. Refer to Supplier Rating System Procedure(BZQP-7-6).采购和QA选择关键供货商进行评估,参照供货商评估系统程序(BZQP-7-6)6.2Material qualification 物料资格认证.6.2.1Under selection of a potential supplier, Sourcing or purchasing sends the specification or drawing componentrequirements to supplier and Engineer instruct supplier to submit sample and related document (Attachment 1.)选定部分供货商后,资材部或采购将部件规格要求或图纸转交给供货商,工程部工程师指导供货商按照提交样品和相关档(附禧1)6.2.2Engineer will cooperate to complete FAI, detail operation process refer to “Incoming First Article InspectionInstruction (BZQAWI-003)”.工程师将完成物料的FAI检查,具体作业方法请参考“来料首件检查指示(BZWIQA-003)”6.2.3After the internal inspection completed, QA submit the passed part and FAI documents to customer for make finalapprove if need. After customer approve the sample, QA distribute the approved sample and relative files to IQC and buyer as the proof of approved by XXX (ZhongShan).内部检查完成后,如客户要求,QA将零件批准的数据(零件样板)和FAI报告送与客户批准.客户检查并批准后,QA将客户最终承认的样板及相关文件分发至IQC和采购,作为样板被乂乂乂(中山)承认的依据.6.2.4If material is rejected by customer, the original copy of material approval should return back to QA. Return processfrom 6.2.1 to 6. 2.4如零件承认被客户否决,则承认零件退回给QA.重复步骤6.2.1至6.2.4.6.2.4.1For the critical to quality indirect material and not customer specified ,new developed suppliermaterial needs to pass Engineer’s approval, and send to customer for approval as required.对于客户未指定的间接物料,在其对产品质量有重要影响的状况下,新物料需要经过工程师批准,如果客户要求将送给客户进行批准.6.2.5Material disqualification procedure.物料资格取消程序6.2.5.1In the below cases, IQC or buyer has the authority to request and disqualify supplier’s part supply, andIQC rise a material disqualification request.( BZQP-7-07F01.1)当发现如下情况时,IQC或采购有权对供货商提出取消其生产件供应资格的申请,并且该申请将以物料供应资格取消申请书形式提出(BZQP-7-07F01.1)6.2.5.1.1Serious quality issue from supplier (example: safety issue, use banned material, or seriouslyimpact production in XXX etc).部品发现重大质量问题(如安全问题,使用禁用物料,或对XXX造成重大生产影响等).6.2.5.1.2More than 3 times claims for material quality from IQC or production line within one month and thereis no effective action to improve the quality after IQC warn or QA perform factory audit.在一个月内IQC拒收三批以上的物料或生产线对该物料有三次以上的质量投诉并且在IQC通知供货商或对供货商进行审核后供货商在质量方面没有有效改善.6.2.5.1.3Continual twice get red card in supplier rating system (for single sourcing supplier, materialis disqualified except customer approval)在供货商级别评定中连续两次评定为不合格(对于单一货源供货商,除非客户批准,否则将取消其资格).6.2.5.1.4Customer requirement 客户要求.6.2.5.1.5Others 其它.6.3 Supplier Qualification & disqualification 供货商资格认证及取消6.3.1For new supplier (or second source) who is opened by XXX (ZhongShan), QA needs to qualify new supplier.For the current suppliers, purchasing can list them directly in the AVL list.对于XXX(中山)开发的新供货商(或者第二供货商),QA需要进行新供货商的资格认证.对于现有的供货商,可直接进入AVL表.6.3.2There are 5 classifications of “supplier qualification” process will be applied:将有5个不同级别的文件被引用到供货商认证中去:6.3.2.1NDA (Non-disclosure agreement):保密协定This is a non-disclosed agreement for supplier with XXX (ZhongShan) before business. Supplier mustobey XXX (ZhongShan) business requirements, can not disclose any XXX (ZhongShan) businessinformation, drawing, technical information, pricing information to any other 3rd party under thisagreement withoutXXX(ZhongShan) permissions.此档是供货商与乂乂乂(中山)生意合作之前的保密协定.供货商必须遵守乂乂乂(中山)商业要求, 不能揭露任何乂乂乂(中山)生意方面信息、图纸、技术信息、价格信息等给任何未经XXX(中山)授权的第三方机构.6.3.2.2Supplier reliable investigate report:供货商信誉度调查This report is to investigate supplier reliable information in market and ensure supplier can show enoughcapability to support XXX (ZhongShan)此文件用以调查供货商的市场信息以保证供货商有足够能力和XXX(中山)配合.6.3.2.3Supplier Qualification Summary Report 供货商认证总结报告This report is conducted by purchasing for one supplier evaluation summary report & qualificationstatus.此份报告由采购主导用以供货商评估总结及认证状况.6.3.2.4Supplier audit report, QA is responsible for perform audit ,if it is necessary and applicable, QA releasesthe copy of report to purchasing.供货商审核报告,QA有必要且可实施状态下将对供货商进行审核,QA将复印件分发至采购.6.3.2.5Supplier Disqualification Request 供货商资格取消申请.This report will be requested by purchasing & QA to disqualify a supplier; and the applicant will fill inthe application. It will be effective by their manager and Plant Manager approval.此份报告由采购及QA用以供货商资格取消申请.由各自部门经理和厂长签名后生效.6.3.3Primary opportunities for one qualified supplier:供货商认证的首选机会:6.3.3.1 A well developed quality management system.优秀的质量发展管理系统.6.3.3.2Reasonable price and forwardly to support XXX (ZhongShan) on cost down approach.可以接受的价格水平并主动配合乂乂乂(中山)降低成本.6.3.3.3Capability of ensuring stable and punctual material supply chain system.能够保证稳定而准时的供应链系统.6.3.3.4Good service can support XXX (ZhongShan) at emergency; provide XXX (ZhongShan) on reliable &acceptable information; quickly respond on claims & remarks; support XXX (ZhongShan) on flexibility;forwardly to provide XXX (ZhongShan) on Information (News, Technical support).优良的服务;能够在紧急状况下支持XXX(中山);提供给XXX(中山)合理的和可以接受的信息; 迅速回馈XXX(中山)的抱怨及相关要求;弹性地服务XXX(中山);主动配合XXX(中山)有用的信息(新闻、技术支持).6.3.4Buyer gathering information of supplier: company profiles, brochures; products information (samples, specs),etc. If it matches current business requirments, then will send “Supplier Reliable Investigate Report” tosupplier for self-evaluation, request supplier to submit self-evaluation data to purchasing for evaluation, based oncurrent commodity supplier base status, technology, quality, cost, responsiveness, service, delivery, stability&capability, environmental & safety, If recommended supplier matches XXX’s requirements, purchasing willlead the “Development team” to audit supplier.采购收集供货商信息:公司资料及手册;产品信息(样品、规格)等如果供货商符合当前XXX(中山)商业需求,负责采购将“供货商信誉度调查报告”发给供货商进行自我评估;要求供货商提供自我评估数据并回馈给采购,采购依据XXX现有商品供货商基础、技术、质量、成本、反应速度、服务、交期、稳定性和能力、环境及安全等予以综合评估.如果推荐的供货商符合乂乂乂(中山)要求,采购将安排发展团队予以评鉴.6.3.5Purchasing will lead “development team” to summarize “Supplier Qualification Summary Report”,to evaluaterecommended supplier will be qualified supplier. XXX (ZhongShan) qualified supplier must be required:采购将主导“发展团队”总结“供货商认证总结报告”,以评估推荐供货商成为合格供货商.XXX (中山)合格供货商必须同时满足如下要求:6.3.5.1Pass XXX (ZhongShan) QA audit if it is applicable. The approval classification will refer to “BZWIQA-015supplier audit &qualification”.在审核可以进行和需要的条件下,供货商须通过乂乂乂(中山)。
仓库物料处理管理程序-中英文对照
Revision History1.0 PURPOSE目的1.1 To establish a procedure of handling, storage, packaging, protection and delivery, whichincludes receiving & dispatching of equipments, parts, raw materials, materials and finishedgoods from SUNMING store.建立SUNMING仓库物料处理,储存,包装,防护和交付的程序,包括设备,部件,原材料,和成品的接收和分发。
2.0 SCOPE范围2.1 This procedure applies for equipments, raw materials, & finished goods needed to support theSUNMING internal team and customer requirements.本程序适用于SUNMING内部需求的设备,原材料,以及成品和客户的要求。
3.0 DEFINITIONS & ABBREVIATIONS定义和缩写3.1 Material物料“ Material” here is defined as all tangible objects. Material can be segregated into the broad categories:物料在这里被定义为所有有形的物品。
物料可广泛分为如下类别:3.1.1 Direct Materials - parts that are applied directly in the manufacture of a product and canbe allocated in terms of cost to a product.直接物料-被直接应用在产品制造和被分派到产品成本中的材料。
进料检验作业流程图中英文版
流 程Flow path负责单位Duty dept.说明Description 库管员Librarian 1:供应商送货到我公司附送货单(订单、名称、数量、产品检测报告),仓库接收。
1.The supplier shall deliver the goods to our company's attached delivery list (order, name, quantity, product testreport), which will be received by the warehouse.库管员Librarian 2:仓库点收并确认接收后,如有紧急物料在收货单上标识,将供应商送货单交给IQC检验员,检验人员依照送货单零部件名称按AQL抽样水准去待检区抽样检验。
2: After the warehouse receives and confirms receipt, if there is urgent material on the receipt, the supplier delivery note will be handed over to the IQC inspector. The inspector will go to the inspection area according to the AQL sampling level according to the name of the delivery part. Sampling test.质量部Quality dept.IQC根据物料紧急程序安排检验计划IQC检验员根据产品名称,及图纸或SIP要求,选择合适的量检具,对产品进行检验IQC arranges inspection plans based on material emergency procedures The IQC inspector selects the appropriate gauge according to the product name, and the drawing or SIP requirements toinspect the product.质量部Quality dept.4:IQC需参照相对应零部件名称的图纸并依照SIP内容进行尺寸/性能等检验 。
物料审核放行标准操作规程(英文)
standardize the release of materials, and avoid the occurrence of quality accident.2. Applicable Scope: The procedure is applicable to review and release of materials.3. Responsibilities: QA supervisor and QA inspector shall be responsible for implementation of theprocedure.4. Contents:4.1 QA inspector and QA supervisor shall be responsible for review and release of materials.4.2 Contents of review before release of materials4.2.1 Sentinel procurement: The material supplier shall be the sentinel procurement unit approvedby the enterprise.4.2.2 The materials shall be qualified in the initial inspection, and the records shall be complete andcorrect.4.2.3 The approved operation procedure shall be executed in sampling, and the sampling sheet shallbe complete and correct.4.2.4 The approved inspection procedure shall be executed in inspection.4.2.5 According to “Inspection Requisition”, check whether all records are consistent, and whetherthe name, lot number and quantity in lot inspection record are consistent with the “Inspection Requisition”.4.2.6 According to quality standard, check one by one whether the lab test result conforms to thequality standard and check the operator’s signature/date, and the signature/date of the checker or the person in charge.4.2.7 The inspection report contents shall be accurate and complete.4.3 Procedure for review and release of materials4.2.1 QA inspector checks the sampling sheet, “Inspection Requisition” of materials, supplier’s labreport/ certificate of conformity, and inspection report, and according to the qualification inspection report of materials issued by lab, review that the material supplier shall be the supplier qualified in auditing.4.2.2 QA inspector shall issue the “Certificate of Conformity” and “Material Review and ReleaseSheet”;4.2.3 After they are approved by QA lab supervisor, QA inspector shall issue them and thequalification inspection report of material to the warehouse, and the materials are approved to be released for use.Document Name: Standard Operation Procedure for Review and Release of MaterialsDocument No.: SOP-QU-02-001-00 Page: 2 / 24.3 QA inspector shall supervise the warehouse personnel to paste the certificate of conformity onthe package of material (one for each lot). The warehouse shall decide the issue of materials according to “Inspection Report”, “Material Review and Release Sheet” and “Certificate of Conformity”.5.Keeping and Management of Relevant Records: “Certificate of Conformity” will be discardedas the outer package of material is discarded, and will not be saved; “Material Review and Release Sheet” shall be preserved in warehouse, and managed by warehouse keeper.6. Supplementary Provisions:Department head.。
物料管理程序中英文版
1.0 P URPOSE 目的1.1 To establish management procedure for materials and goods, including receipt, issuing/deliveryand storage process建立物料管理程序,包括物料的收发存。
1.2 To standardize warehouse operation and make sure inventory accuracy。
规范仓库作业,保障库存准确度。
2.0 S COPE 范围2.1 This procedure could be applied to all material and goods in plant, including raw material,package material, spared parts and consumable material ,scraped material, semi-finished-goods and finished-goods, but excluding fixed assets, office stationary ,consumable for laborprotection and facility or soft ware for IT本程序适用于工厂所有物料,包括原材料,包装材料,消耗性材料,废料,半成品,及成品,但不包含固定资产,办公用品,劳保用品及信息设施软件。
3.0 D EFINITIONS定义No无4.0 R EFERENCE DOCUMENTS参考文件4.1 PD-S5-01 Product Monitoring and Measurement Procedure产品监视与测量程序4.2 PD-S6-01 Nonconforming Product Control Procedure 不合格品控制程序4.3 PD-C4-01 Planning Management Procedure 计划管理程序5.0 R ECORDS 记录5.1 FN-LG-01 Finished goods Shipment Form 销货单5.2 FN-LG-07 Make Order生产工单5.3 FN-LG-05 Material Issue Form 领料单6.0 R ESPONSIBILITY职责6.1 Warehouse is responsible for material and goods receiving, issuing/transfer ,storage, andhighlight abnormal material in warehouse仓库负责物料的收,发,存,以及异常物料的提报。
PPAP生产件批准程序中英文版(含流程图)
1.0目的(Purpose)確定本司是否已經正確理解了客戶工程設計記錄和規范的所有要求,并保證在實際生產過程中,具有持續滿足這些要求的潛能 .To make sure whether we can understand all of customers’ engineering design record and standard requirem ent. We also can assure that we have potential to keep customers’ requirement during the real process of production.2.0范圍(Scope)適用於本公司向客戶提交生產件(生產材料、生產件和維修件)過程的控制.如客戶不要求按QS9000提交PPAP,則依客戶要求作業.It is applied to control the process of production parts ( production material, production parts and repaired parts ) approved by customers.if the customer don't require us to submit the PPAP accord to the QS9000,we will accord to the customer.3.0定義(Definitions)3.1 生產件: 生產現場使用的工裝治具﹑過程﹑材料﹑操作者﹑環境和過程參數 .Production parts: The fixture, process, material, operator, environment and the parameter of process used in the line3.2 新產品: 廠內從未打樣或生產過,或亦無與其類似的產品(包括規格﹑性能及外觀) .New product: The product never produce or trial run in our company, we also don’t have any similar pr oduct ( including spec, function and aspect ).4.0職責(Duties)4.1專案工程(PM): 成立新產品負責小組﹑召開新產品說明會﹑新產品生產安排與跟催﹑異常處理及內部PPAP所有項目的審核 .PM: To build the new product project team, hold new product announcement meeting, arrange new product produce schedule and track, handle abnormality and handle all internal items of PPAP audit.4.2生技課: BOM建立﹑GERBER的分析確認﹑線路圖分析﹑來料確認﹑首樣CHECK、產品測試規划﹑測試人員訓練﹑設備請購與確認.PE: Build BOM, analyze Gerber and schematic, check incoming material and first product, plan product testing, train testing staff, apply and confirm fixture.4.3工業工程: 組裝過程﹑量具﹑操作規范制定和技朮參數制定 .IE: Define the standard of operation, procedure of assembly, fixture and set up the parameter of technology4.4生產: 包括SMT課,AI課及MI課,其職責是操作規范﹑技朮參數﹑執行以及組裝過程的驗証.PD: include SMT, AI and MI, their duties include the standard of operation, examine and execute the process of assembly, and the parameter of technology4.5品保: 進料確認及其操作規范的驗証與監督,SPC和GR&R 之推行與實施以及客訴基板維修.QA: incoming material inspection and audit, execute SPC and GR&R,and repairing the product that customers complain .4.6企划: 料況追蹤確認﹑生產安排及出貨日期的排定 .PMC: Checking Material shortage, production schedule and shipping date4.7采購: 材料的訂購及追蹤作業 .PUR:material purchase and tracking4.8文管中心: 相關文件的發行及管制 .DCC: Related document release and control5.0作業流程(Flow Chart)PPAP作業流程圖參見附件1 .The flow chart of PPAP. See the attachment 16.0作業程序(Work Procedures)6.1 PPAP 提交時機The timing of PPAP本公司將對下列情況獲得客戶產品批准部門的完全批准:We should get customer’s approval when the following situations happen.6.1.1一種新的零件或產品.A new material or product6.1.2.對以前提交零件不符合的糾正.Correcting the former material wrong spec.6.1.3.由于設計記錄﹑規范或材料方面的工程更改引起產品的改變.Product change due to the record of design, regulation or material’s engineering change6.1.4.客戶通知和提交要求的任一種情況.Either c ustomer’s notice or submit requirement6.1.4.1客戶通知 customer notification本公司將<表一>中列出的任何設計和過程更改通知客戶產品批准部門,由客戶產品批准部門決定是否提交PPAP批准.In sheet 1, company list any design and process change that need to notice the department of customer product approval. The department of customer product approval decide If its need to approve by PPAP<表一> Sheet 16.1.4.2 客戶提交要求The request to submit custom若為<表二>情況之一,本公司在首批產品發運前提交PPAP批准,除非客戶負責產品批准的部門放棄了該要求. 不論客戶是否要求正式提交,本公司會在需要時對PPAP文件中的所有適用的項目進行評審和更新,并由PM經理作為內部PPAP之提交客戶, 擔任PPAP所有項目的審核,以反應生產過程的情況. 經客戶批准的PPAP文件必須包括客戶產品批准部門負責核准特許人員的姓名和日期 . 若客戶不要求提交PPAP中某個或某些要求項目時,則本公司保留客戶不要求提交的証據, 本公司不作提交. 若客戶要求在生產件批准前進行FMEA 評審和批准,則提交.If one of the situation in sheet 2, our company will submit PPAP to customers for approval before first batch be produced, un less customer’ department which responsible to approve product gives up the request. Whether customer ask for a formal submission or not, we will review and renew all suitable items that listed in PPAP if necessary. Then, PM manager will be the internal customer for PPAP submission and responsible to audit all PPAP’s items and reaction the situation of production process. The PPAP which approved by customers should includin g the name of staff who responsible to approve product in customer product approval department and date. If customers don’t request one or more items in PPAP, our company will keep the evidence to prove customers don’t need it and our company won’t submit it. If customers request to review and approve FMEA before Production Part Approve, our company will submit it.6.1.4.3客戶不要求通知的情況The situation that customers don’t need to be notice在<表三>中所描述的情況不要求通知客戶和提交.本公司有責任跟蹤更改和/或改進并更新任何受到影響的PPAP文件.但是,任何情況下,一旦影響到客戶對裝配性﹑成型﹑功能﹑性能和/或耐久性的產品要求,則本公司要求通知客戶.The situation that customer don’t need notice and submission which listed in sheet 3. Our company is responsible to track, revise or improve PPAP. However, once the change affects the product requirement for assembly, shaping, function, durability or performance in any situation, we have to notice customers.6.2 PPAP提交等級確定 To decide the rank of PPAP submission6.2.1 客戶提交要求----証據的等級The requirement of customer submission---the rank of evidence6.2.1.1客戶要求提交PPAP時,本公司會由PM按客戶要求的等級,提交該等級規定的項目和/或記錄,具體提交等級如下:Our company will submit the required items and record based the rank of customer request when customers ask for PPAP. The rank as bellows:等級1 ---- 只向客戶提交保證書(對指定的外觀項目,還應該提供一份外觀批准報告);Rank 1—only submit warranty to customer (beside the assigned outlook items, we should provide a outlook approval report)等級2 ---- 向客戶提交保證書和產品樣品及有限的支持數據;Rank 2 – Providing warranty, sample and the limited support statistics等級3 ---- 向客戶提交保證書和產品樣品及完整的支持數據;Rank 3—Providing warranty, sample and the completed support statistics.等級4---- 提交保證書和客戶規定的其它要求;Rank 4—Providing warranty and other requirement of customer regulation等級5---- 在本公司制造廠備有保證書﹑產品樣品和完整的支持性數據以供評審.Rank 5—There have warranty, sample, and the completed support statistics in our factory for customers review 6.2.1.2若客戶負責產品批准部門沒有其他的規定,則本公司使用等級3作為默認等級 .If the customers’ product approval department no other regulation, we will use rank 3.6.3 保存/提交資料本公司PPAP保存/提交資料之項目參見“PPAP 保存/提交資料確認表”.PPAP 保存/提交資料確認表6.4試產前資料收集The information collection before trial run試產依《產品質量先期策划程序》和“PPAP 保存/提交資料確認表”,進行試產前資料的准備工作 .Trial run should follow up Procedure of Advanced Product Quality Planning and “PPAP Preservation/ Proposition Checking Sheet” to do theinformation preparation before trial run6.5 試產及相關資料收集Trial run and related information collection6.5.1 新產品作業依《產品質量先期策划程序》和“PPAP 保存/提交資料確認表”進行相關收集資料.New product operation should follow up Procedure of Advanced Product Quality Pplanning l planned “PPAP Preservation/ Proposition Checking Sheet” to collect related information6.5.2 已生產過的產品依《過程控制程序》作業,并收集相關資料.Product that has bee procedure should follow up the Procedure of Process Control to collect related information6.6 PPAP資料整理PPAP information arrangements當客戶要求提交時,則將客戶所需資料經產品專案主導者核准後透過PM傳給客戶;若客戶未要求 ,則經本公司內的顧客代表(即PM經理)批准,并在相關單位妥善保存.When customer request parts approval, project leader approve the report that customer need and pass it to PM, and then PM fax it to customer, If customers don’t request it, it just need internal repres en tative’s (PM) approval and is kept in the related Department properly.6.7零件提交狀態The status of parts approval6.7.1 提交總則:生產件經客戶批准之后,對於客戶針對提交所作出的處理結果,本公司會持續改進,保証將來的生產持續滿足客戶的所有要求 .The general rules of submission: After parts approved by customer, our company will keep improve based on customers’ solution for submission and assure our production will keep satisfying customer request in the future.6.7.2 客戶PPAP狀態The status of customer’s PPAP6.7.2.1完全批准. 是指該零件或材料滿足客戶所有的規範和要求.當PPAP完全批准時,本公司可根據客戶計劃部門的安排按批量發運產品.Completed Approval: The parts or material can satisfy all of customer’s standard and requirement. When PPAP be approved compl ete, we can ship product by batch according customer plan department’s schedule6.7.2.2臨時批准:PPAP臨時批准時,則按客戶要求作業,并確認臨時批准原因,再作重新提交作業,以獲得“完全批准”.Temporary Approval: When PPAP is approved temporary, we should follow up customers’ requirement and check the reason of temporary approval. And then, we submit the PPAP again to get the completed approval.6.7.2.3拒收: PPAP拒收時,則需與客戶確認原因及后續處理方式,按客戶的處理方式作業,並將更改的產品PPAP重新提交客戶批准.Reject: When customers reject PPAP, we should confirm with customer about the reason of rejection and follow up customers’ operation.And then revised PPAP and submit to customer for approval.6.8 提交批准之PPAP資料的保存The preservation of PPAP information6.8.1無論提交的等級如何,生產件批准記錄的保存均須按《質量記錄控制程序》的相關規定執行, 保存時間必須為該零件在用時間 ..No matter which rank of PPAP submission is, the preservation of PPAP should follow up Procedure of Quality Record Control and the preservation time should be the time the component is using in hand6.8.2本公司確保在新零件的PPAP文件中包括或引用了來自被替代零件PPAP文件中的適用的PPAP記錄.Our company assures the PPAP of new parts include or quote the PPAP record in substitute parts PPAP6.9當客戶對生産件認可有特殊特性要求時,按客戶的要求執行,由PM組織落實。
Material And Goods Management物料管理程序(中英文)
1.1To establish management procedure for materials and goods, including receipt, issuing/delivery and storage process建立物料管理程序,包括物料的收发存。
1.2To standardize warehouse operation and make sure inventory accuracy。
规范仓库作业,保障库存准确度。
2.0 SCOPE 范围2.1This procedure could be applied to all material and goods in plant, including raw material, package material, spared partsand consumable material , scraped material, semi-finished- goods and finished-goods, but excluding fixed assets, officestationary ,consumable for labor protection and facility or soft ware for IT本程序适用于工厂所有物料,包括原材料,包装材料,消耗性材料,废料,半成品,及成品,但不包含固定资产,办公用品,劳保用品及信息设施软件。
3.0 DEFINITIONS 定义No无4.0 REFERENCE DOCUMENTS 参考文件4.1PD-S5-01 Product Monitoring and Measurement Procedure 产品监视与测量程序4.2PD-S6-01 Nonconforming Product Control Procedure 不合格品控制程序4.3PD-C4-01 Planning Management Procedure 计划管理程序5.0 RECORDS 记录5.1FN-LG-01 Finished goods Shipment Form 销货单5.2FN-LG-07 Make Order 生产工单5.3FN-LG-05 Material Issue Form 领料单6.0 RESPONSIBILITY 职责6.1Warehouse is responsible for material and goods receiving, issuing/transfer,storage, and highlight abnormal material inwarehouse仓库负责物料的收,发,存,以及异常物料的提报。
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1.PURPOSE 目的:To establish a procedure for reviewing and disposing non-conforming materials, semi-product, finished products and RMA control in Beckett (ZhongShan).本程序规定对来料检验及生产过程中发现的不合格物料,半成品,成品及客户退回品的评审及处置方法.2.SCOPE 范围:This procedure is only applicable toXXXX (ZhongShan).本程序适用于XXX(中山)公司.3.DEFINITIONS 定义:3.1 PRD: Product Department 生產部3.2 ME: Manufacture Engineering 制造工程3.3 RTV: Return To Vendor/Supplier 退回供應商3.4 UAI: Use As It Is 讓步接受3.5 SORT: Segregation Of Bad And Good Unit 選用3.6 SCAR Supplier/Sub-contractor Corrective Action Request (8D) 供應商改進行動要求(8D)3.7 GRN: Goods Receipt Note 收货单3.8 MRR: Material Review Record 物料评审记录4.REFERENCE DOCUMENT 参考文件:4.1 BZQP-7-05 Raw Material Quality Control Procedure原材料质量控制程序4.2 BZQP-8-05 Nonconforming Control Procedure 不合格品控制程序4.3 BZQP-8-06 Stop Shipment and Purge Order Procedure停止出貨和清除指令程序.4.4 BZQP-8-07 Corrective and Preventive Actions Procedure 纠正及预防措施程序.5.RESPONSIBILITY 职责:5.1 QA is responsible to chair MRB meeting when defective material are defected in line, QA review the non-conformingproducts and issue SCAR (8D) if necessary.当不合格物料在产线发现时,QA负责主持MRB会议, 确认不合格产品, 并在必要的情况下发出SCAR(8D).5.2 PRD is responsible to fill MRB label and inform QA members to review the non-conforming products, andreturn them to warehouse.生产部负责填写MRB标签并通知品质部成员评审不合格品, 并将不合格品退回货仓.5.3 PUR/ IQC are responsible to inform supplier of the non-conforming data, PUR responsible to arrange thenon-conforming materials RTV.采购/IQC负责将不合格批物料状况通告客户或供货商, 采购还负责安排将不合格品退回供货商.5.4 PUR is responsible to charge the supplier of sorting/reworking cost and other loss due to material quality issue,and call MRB meeting to review the reject lots of IQC raised.采购负责向供货商索取选用或重工费用及由于物料问题而导致的损失, 并召集MRB会议处理IQC拒收的紧急物料.5.5 ME is responsible to analyze non-conforming products.ME负责分析不合格品.5.6 All MRB members are to propose and decide on defective material disposition and carry out the follow-upactions as agreed in the meeting.所有MRB成员负责执行MRB会议之决议,并跟进MRB会议决定的所有行动措施.5.7IQC is responsible to confirmed material which is suspected has defect. And IQC drive supplier to takecorrective action if necessary .IQC负责对被怀疑的物料进行确认,并且在必要的情况下,将要求供货商对其进行改善.6.PROCEDURE 程序:6.1MRB team consist MRB小组成员Normally, MRB team consists QA, PRD, PMC, PUR managers or whose dictated representative, if necessary other related members also can attend the meeting (such as supplier, customer etc.).通常, MRB小组由品质部、生产部、物料部、采购的部门经理或其指定代表组成, 如有必要其它相关的成员也应参加(例如供货商, 客户等).6.2Incoming Inspection Reject 來料檢驗不合格6.2.1When the incoming lot is rejected by Beckett (ZhongShan), IQC for quality or other causes, it shouldbe marked on the GRN sheet.当来料检验批判定不合格后,由IQC注明于收货单.6.2.2The rejected lot will be put into IQC Reject area by WH. If the coverage of defects is beyond IQC area,IQC shall work with QA to consider raising a purge order.不合格物料由货仓转移至IQC拒收区隔离存放, 如果不合格不仅仅发生在IQC, IQC需会同QA发出清除指令.6.2.3IQC fill in MRB form to QA manager and related departments for reviewing the rejected lot, the resultmaybe as below:IQC开出MRB单给品质经理及相关部门对不合格物料进行评审, 处理结果有如下几类:6.2.3.1RTV: Per PUR confirm, the rejected lot can be returned to supplier, this decision should bemade, the MRB decision should be noted on the MRB form, it must be approved by the QAmanager or whose representative at least.RTV: 经采购确认, 如果不良批可退返供货商, 应做出RTV的决定, 此决定需注明于MRB单上, 且至少由QA经理或其指定代表签署.6.2.3.2UAI: Use as it is. If the material lot is very urgent to the production and according to theevaluation of MRB members, the defect/nonconformity will not lead impact/defect to ourfinished product quality, the decision of UAI may be made and recorded on the MRR sheet, itneed be approved by the QA manager, ME, and PUR. or whose representatives of otherdepartment, it needs Production manager’s approval if necessary.QA and ME should monitorthe effect of UAI material using.Note: if the defect maybe cause finished products quality issue, it must be promised by ourcustomer first, then can be made the UAI decision.UAI: 让步接受.如果该物料为生产线急需并根据MRB成员的评估不会对成品质量产生影响, 则可做让步接受, MRB评判结果记录在MRR单上, 且至少有QA经理,采购和工程部或其部门经理的指定代表签署,必要时需生产经理签署。
. QA和ME应监控生产中使用效果.注意: 如果此不良有可能影响到成品的质量问题, 则必须得到客户的许可才能做出让步接受的决定.6.2.3.3Sort/R ework: If the material is urgent for produce, and for MRB evaluation the defect will befull eliminated by easy sort/rework, the SORT/Rework decision will be made based on thenegotiation with the supplier, the MRB result should be recorded on the MRR sheet, it must beapproved by the managers or whose representative of QA, ME, PRD, PUR. Thesorting/rework responsibility by either a specified department or supplier. Namely, sortinternally or sort externally.选用/返工: 如果该物料为生产线急需, 且经MRB小组判定经简单加工/挑选即可完全消除不良缺陷, 根据与供货商谈判的结果可进行选用/返工处理, MRB评审结果记录于MRB单上, 至少有QA经理, ME经理, 生产部经理, 采购或其指定的代表签署, 指定由供货商或相关部门筛选,即分为内部筛选和外部筛选.6.2.3.4Scrap: If the defect can’t be retrieved or the supplier authorizes to scrap the rejected part, thedecision should be recorded on the MRB form. The authorization of scrap must be approvedby the manager QA, PU D at least, if necessary the scrap should be submitted to Plant Managerfor approval.报废: 不可修复的缺陷或得到供货商授权报废的不良品,其决议内容都应记录于MRB单上. 至少由QA经理, 采购经理签署, 如有必要, 报废申请需提交厂长作批准.6.2.3.5The disposition to the material purged out should be confirmed by QA manager.对被清除物料的处置, 物料评审会议结果须由QA经理确认.6.2.3.6If the MRB meeting result is sorting/reworking, an incoming sorting/reworking report shouldBe filled out (Form No:BZQP-7-08F04.1) when it is necessary. When the sort/rework over,IQC must re-inspect the good part upon normal sampling plan. If it’s a supplier problem,Purchaser should raise the charge request of sort/rework cost to the supplier and follow up.如果MRB结果为选用/返工, 必要时需填写物料选用/返工报告(FormNo:BZQP-7-08F04.1), 选用/返工完成后, 需经IQC重新检验. 通常情况下, 如果是供货商的原因, 选用/返工费用由物料供货商支付. 采购负责跟进对供货商索赔结果的落实情况.6.2.3.7If a certain part should be restricted using as per the MRB decision, this part should beidentified with a MRB label and note “UAI” marking.如果MRB会议决定需限制使用的物料, 可让步接受后再加贴MRB标签, 并注明UAI.6.2.3.8IQC inspector will stamp or label the material with corresponding remarks, such as RTV, UAI,Sort, Rework or Scrap as per MRB decision. The receiving person should transfer the materialto the part store accordingly.IQC检验员根据MRB结果对物料进行相应标识,比如退回供应商,让步接受,选用,重工或报废,并由收货人员将其转入相应位置存放.6.3Line Reject Material semi-products / finished products生产过程中不合格品6.3.1For the mass lot non-conforming products were found in process or QA inspection, IPQC should reportto supervisor at once, and QA manager issue line stop order when it is necessary, QA (for finishedproducts) purge out all non-conforming lot products and PQC issue Process Abnormity Handing Sheetto related department for analysis and following up related actions.对于在生产过程中或QA检验时发现的大批量不合格品, PQC向上级紧急汇报,必要时QA经理需下达停线指令, QA(对于成品)需立即清除所有的不合格批产品,PQC开出制程异常处理单给相关部门进行分析并跟进相应的行动措施.6.3.2For the little lot non-conforming products were found in process, PRD should fill MRB label and pastethe label on related materials, then inform ME and QA to review the non-conforming products andmake interim disposition, for semi & finished products, ME should provide FAR (Fail Analysis Report)to support the MRB judged. Then write down the disposition result on the MRB label. PRD staffssorted the non-conforming products with incoming defect and process defect; generally the returnedproducts shall have the original tray or box.对于在生产过程中发现的小批量不合格品, 由生产部填写MRB标签并通知ME和QA对不合格品做评审, 并做出处理结果填写于MRB标签上, 对于成品和半成品, ME需提供不良分析报告,作为MRB裁决的依据, 生产部根据此临时结果将不合格品分为来料不良类和制程损坏类,原则上被退回的不合格品应保持原包装.6.3.3For the process defect products, PRD list them on the “Scrap Material Review List” and submit to PRD,QA managers or whose representative to sign, then return the defective products to WH. WH handlertransfer the defective products to scrap store and replenish the balance to PRD in time. “Scrap M aterialReview List” sheet should be distributed to PRD and WH by PRD members for conservation.对于制程损坏的产品, 生产部将其列入“报废物料审核单”并提交至生产部经理, QA经理或其指定代表签署, 再将不良品退回货仓, 货仓物料员将不良品转入报废仓并及时补料给生产部. “报废物料审核单”由生产部物料员分发至生产部和货仓存档.6.3.4For incoming defect products, PRD list them on the “Incoming Defect Return To Store” sheet, andsubmit to PRD, QA managers or whose representative to sign, then return the defective products to WH,WH handler transfer them to MRB store and replenish good materials to PRD. The “Incoming DefectRetur n To Store” sheet should be distributed to PRD, IQC and WH by PRD members for conservation.对于判定为属来料不良的产品, 生产部将其列入“来料不良退仓单”并提交至生产部和QA经理或其指定代表签署, 再将不良品退入货仓, 货仓物料员将其转入MRB库位并及时补料给生产部,“来料不良退仓单”由生产部物料员将其分发至生产部、IQC和货仓存档.6.4The products returned by customer can be reviewed and dealt with as sort, rework or scrap as per theauthorization of this procedure.对于客户退回的成品,依据本程序评审和处置权限执行挑选,返工或报废.6.5If it is necessary, IQC should issue a SCAR (8D) to supplier for the material defect or where applicable keepcustomer aware o f the disposition of the defective product. Refer to “Corrective and preventive actionsprocedure”.在必要的情况下,IQC应将不良物料状况通知供货商, 并发出SCAR(8D), 参照“纠正及预防措施程序”.7.RECORD 记录:8.FLOWCHART 流程图:9.ATTACHMENT 附件:9.1 BZQP-7-08F01.3 Incoming Defect Return To Store 來料不良退仓單9.2 BZQP-7-08F02.3 Material Scrap Review List 報廢物料审核单9.3 BZQP-7-08F03.1 MRB Meeting Review Record MRB 会议评审记录9.4 BZQP-7-08F04.1. Sorting/Rework Report 全检/加工报告。