QSA Audit(Dell)(工厂稽查)

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DELL QSA中英

DELL QSA中英

Remarks
SPP-002 品質管理之運作
ቤተ መጻሕፍቲ ባይዱ
口号 合适度 持续改进
SPP-002 品質管理之運作
(b) Does the Quality Policy include a commitment to comply with requirements and continually improve the effectiveness of the quality management system?品質方針有包涵依照實際需求不斷改進QMS有效性嗎 (c) Does the Quality Policy provide a framework for establishing and reviewing quality objectives? 品質方針是否為建立和修訂品質目標提供架構 (d) Is the Quality Policy communicated and understood within the organization? 組織內部品質方針是否被廣泛傳播和理解
(Ref 4.2.1) (Ref 4.2.2) (Ref 4.2.2) (Ref 5.5.1)
管審會審查其適宜性
方針管理運作系統; 品保部品質目標 SPP-002 品質管理之運作 SPP-001, 002, QS-01~23, CG*O02-0029 CG-*O02-0029
1.9 Does the quality management system documentation include a quality manual?品質體系包括品質手冊? 1.10 1.11 Does the quality manual include the scope of the quality management system, including details of and justification for any exclusions?品質手冊在品質體系內?之間有矛盾?

供应商体系评估报告(QSA) (2)

供应商体系评估报告(QSA) (2)

Quality Systems/质量体系部
Grading standards 等级标准
General Comment 总评
91% ~ 100%
□ EXCELLENT / 优秀 Quality system is in place and capable to produce Refond product to spedfications. 品质体系较完善且有能力生产Refond的产品.
□ YES
Who is in charge of the QA supervisor(List out the person’s position) 2 品保部主管属于谁管(列出此人的职位)
List out the following number of staffs who are under the QA in charge:
Assessed Item/Procedure is included. Planning and execution MEETS requirements. 3 品质体系包含了调查的项目/程序, 计划和实施均符合要求。
Assessed Item/Procedure is included. Planning and execution is thorough and OUTSTANDING. 4 品质体系包含了调查的项目/程序,且计划和实施均都执行得非常好。
Address : 地 址:
Company Name(Include Brand): 商品名(包括品牌):
Nationality: 国家:
Tel: 电话:
Fax: 传真:
Supplier’s Representatives/供应商填表人
Position in Company/公司职位

QSA检查内容

QSA检查内容

Qua价工程 区分 4.1 制品仓库管理状态 细部评价项目 判定 Notes and Comments
制品管理 4 区分 必须 全体 配點 1 6 評點 1 6
일반 일반 4.2 일반 필수 일반 4.3 일반 5.1 필수 5.2 評點 0 0 일반 일반 5.3 일반 6.1 일반 일반 필수 일반
No 评价工程 区分 일반 필수 일반 일반 일반 일반 일반 필수 필수 필수 工程管理 7 일반 필수 필수 일반 일반 细部评价项目 7.1 工程检查实施状态 √检查周期, 工程, 数量, 检查者选定等工程检查基准设定与否? √工程检查是否按基准实施? √对工程检查时检出的不良是否树立改善对策? √对于改善对策实施与否是否进行检点记录? √对于不良检出的 Lot 是否实施在检查? 7.2 CTQ 工程管理状态 ( CTQ: Critical To Quality ) √CTQ 工程上是否选定了管理项目? √CTQ 工程是否标注 "CTQ工程" 这个标识? √CTQ 管理项目是否周期性的进行检点? (日 3回以上) √CTQ 测定 Data是否每日登陆到 SQCI System上? √CTQ 测定 Data是否是虚假的? ( 现场确认 ) 7.3 Cpk 管理状态 √Cpk 测定周期及试料适当与否? (Time别 5EA 以上/Cpk Data 产出 = 30个以上) √是否每日测定 Cpk 后日别管理 Trend ? ( SQCI System 登陆管理 ) √Cp/Cpk 值管理超出时是否进行原因分析及采取措施? 7.4 Line-Stop 运营状态 ( 关于资财品质的 Line Stop 除外 ) √有无 Line-Stop 运营基准,并 Stop 基准设定与否? √实际是否实施 Line-Stop 并改善对策树立后进行再启动? 7.5 工程不良改善活动充实度 √工程不良是否由指定的担当进行每日的回收/分析? 判定 y y y y y y y y y y y y y y y 工程不良是没有指定的担当进 行每日的回收/分析 工程不良统计,分析不全面 Notes and Comments

CQM工作职责

CQM工作职责

SQE工作职责1制定完善供应商质量管理制度、办法和规程;2监督并执行供应商质量管理;3 通过SCAR方法改进供应商质量;4 负责对供应商的体系审核及生产流程审核工作;5 负责对供应商供货质量的统计及评价工作,并对供方的持续改进予以监控;6 及时,有效地处理供应商的质量投诉问题;7 负责对供应商的业绩进行综合评价、定级并体系开发工作;SQE供货商管理工程师1、必须要有供应商跟踪的方式,质量问题独立处理的方法;2、高级职位必须要有成本控制、质量控制管理的清晰思路与意识、坚持的原则底线;3、供应商的内部品质管理流程、以及可能出现的问题对应方式。

4、稳定性的保证手段。

针对此四点职责,以下是我的一点经验:1. 对供应商例行品质绩效评估与稽核;1.1 导入新厂商:一般内容有:对新供应商作总况调查、QSA(Qaulity System Audit), QPA(Quality process Audit)、签定品质合约;1.2 供应商例行品质绩效评, 每月评分与制程稽核QPA;每月评分三要素TQR: Technology. Quality. Response;每月一评,评分结果分A/B/C/D 等级。

1.3 制程稽核(QPA)每季度末由SQE 制定下季度的稽核计划.制程稽核方式:针对不同的站别, including Receiving Inspection 、Warehouse 、MRB 、P/L 、Secondary Operations、OQC、Packing and Stock and so on.总结起来,重点项目由人、机、料、法、环五项构成,具体事项按公司QPA List 点检。

人:1. 培训 2. Comply WI/SOP ;机:3 设备/校验。

4 治具/测量;料:5. 物料分区. 6 保存期/保存方式;法:7 可追溯性; 8. SPC, 自检, CLCA 检讨;环:9 安全防护. 10 湿/温度;QSA 通常每年一评。

DELL专用术语解析

DELL专用术语解析

持续精进优化系统品质
品保总处 系统品质
DELL专用术语解析
缩写 QPA QSA SPC SQE 英文全称 Quality Process Audit Quality System Audit Supplier Quality Engineer 中文解析 品质过程稽核 品质体系稽核 协辅工程师 品质持续改善计划
DELL专用术语解析
—体系DELL化宣导文宣一
持续精进优化系统品质
品保总处 系统品质
DELL专用术语解析
缩写 AFR ARR 英文全称 Annualized Failure Rate Annualized Return Rate 中文解析 年度不良率 年度返品率
DPP M
DVT
ECO EVT
Defective Per Million
FMEA Failure Mode Effect Analysis
GQA M
Global Quality Account Manager
全球品质经理
持续精进优化系统品质
品保总处 系统品质
DELL专用术语解析
缩写 英文全称 中文解析 量具重复性和 再现性 进料品质管制 GR&R Gauge Repeatability and Reproducibility IQC Incoming Quality Control
Statistical Process Control 统计制程管制
IPQC In Process Quality Control 制程品质管制 QCIP Quality Continuous Improvement Plan
持续精进优化系统品质
品保总处 系统品质
Design Validation Testing

如何执行供应商QSA.QPA稽核

如何执行供应商QSA.QPA稽核

Either review by document or by meeting, conf call, on site review….., etc.(稽後審查會議)
Issue the follow up status and comment the result. (審查 結果報告 )
QSA 稽核查檢表雷達圖
Well arrange the auditee candidate and the schedule (與陪稽人員按表操課)
During the auditing
Based on the audit agenda, item by item, control the schedule is very important.(控制時間) Simply ask the item you want to know, never ask Yes/No question, ask deeply how? Why? Why? Pls show me. To get the root cause and check the evidence.(開放式問答How…並至少問二個Why…) Write down the nonconformity clearly with where, who, what, when, ..(詳實紀錄人事時地物) Clearly deliver what you think and want, don’t need to make conclusion once both have different opinion.(充 分溝通問題與建議)
How to perform a vendor audit of QSA & QPA? (如何執行供應商QSA/QPA稽核 ?)

Dell供应商质量体系审核

Dell供应商质量体系审核

Dell供应商质量体系审核Modul1QualityRecord HandlingPkgStorageDelivery NonconformityControlCalibrationInspectionProcessControlProductID&LotTraceability SupplierQualityDocumentControlDesignControlContractReviewQualitySystemAuditSummaryInstructions__DemandLoad Blatt1Blatt11Blatt12Blatt13Blatt3 Folgeseiten Print_Area Print_Area Print_Area Print_Area Print_Area Print_Area Print_AreaPrint_AreaPrint_AreaPrint_AreaPrint_AreaPrint_AreaPrint_AreaPrint_Area INDEX DesignControl DocumentControl SupplierQuality ContractReview DiscussionORTModul1.QdataQdata1Qdata2SPC1 Nonconforming Calibration Inspection QualityRecord Handling ProcessControl ProductID PrintPresentation QualitySystem AuditSummary 信息和指示目的这份文件是作为一个审计工具,以评估供应商的质量体系对戴尔的质量体系要求。

TheDellQualitySystemsAudit(QSA)isbuildupontheISO-9000QualitySystemsStandard,butwithadditionalDellspecificrequi rementsincluded.范围戴尔质量体系审核不是具体的商品,因此它可以用来评估由供应商/生产商部署的质量体系,不论商品如何.。

品质体系稽核表(QSA)汇总.

品质体系稽核表(QSA)汇总.

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该项得分百分比: [
]
2 管理职责、资源管理
该项得分:
[
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该项总分: [
]
A类
2.1 是否建立并发布由最高管理者批准的质量方针、质量目标。质量目标是否与质量方针的总体要求相一致。质量方针是否体现持续改进。(需包含有害物质的管理)
5.15 试的产品有否采取适当的方式区分、标识,以避免混乱。
V
V
V
V
5.16 是否有产品标识和追溯的管理办法,并有效实施,在有可追溯性要求的场合,组织应控制产品的唯一性标识,并保持记录。生管对工单进行控制并可追溯。
V
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5.9 当制程失控和生产异常,是否有一个停线标准或停止出货标准。
V
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5.10 有无品质反馈系统,如制程品质收集分析等,并贯彻执行。
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5.11 操作人员是否掌握工艺要求或作业指导书,并按其要求进行操作。作业员是否清楚本制程的安全质控点。
V
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5.12 客户样品是否进行明确的标识并妥善保存,样品的有效期是否列入管制清册。是否有样品测试流程和项目LIST。

Q2-021外包厂HSFA、QSA、QPA作业管理办法

Q2-021外包厂HSFA、QSA、QPA作业管理办法
4.1 HSFA: Hazardous Substance Free Audit Assessment (有害物質管理系統評鑑) 4.2 QSA: Quality System Audit Assessment(品質系統評鑑) 4.3 QPA: Quality Process Audit Assessment (製程能力評鑑) 4.4 EMS: Electronics Manufacturing Service (電子製造服務) 4.5 CQM: Commodity Quality Management (產品品質管理)人員 4.6 SQM: Supplier Quality Management (供應商品質管理)部門/人員 4.7 GSM: Globe Supplier Management (全球供應鏈管理)部門/人員 4.8 EQM: EMS Quality Management (外包廠品質管理) 部門/人員 4.9 QBR: Quarterly Business Review (企業季度審查) 5. 作業程式與權責: 5.1 稽核時間
5.5.6 HSFA/QSA/QPA 稽核結果將列入 QBR 評比項目中。 5.6 ASUS HSF 優良外包廠證書頒發與取消:
5.6.1 獲得證書資格:當同一外包廠連續 2 次於 ASUS HSF 稽核總平均評鑑結果 ≧90%(判定為 Pass),其方可具備 ASUS HSF 優良外包廠資格。
5.6.2 證書將由 ASUS 品保中心頒發之。 5.6.3 當有以下情況發生,外包廠獲得之 ASUS HSF 優良外包廠證書將立即失效:
6758emshsfaqsaqpa?程稽核小組eqm人員ems稽核總稽核員emsgsmpm提出ems廠稽核要求擬定稽核計劃或????稽核計劃通知ems預計稽核?程回覆陪稽人員稽核結果為pass回覆稽核結果給華碩sqm通知主導稽核員排定具體稽核?程稽核前會議?加稽核前會議限期改善?符合項目?符合項目記??符合項目cqm通知emsgsmpm進??符合項目改善並回覆稽核缺失報告安排複稽?程外包品保主管找gsmpm開會討?後續處?事宜判定結果pass進??符合項目改善並回覆稽核缺失報告yes進?稽核fail判定結果改善效果ng稽核結果為fail

供应商稽核查检表(质量体系稽核)

供应商稽核查检表(质量体系稽核)

(Ref 7.2.2.)
2.8
(f). 对风险和可能发生的意外的识别
(Ref 7.2.2.)
2.9
(g). 对产权信息足够的保护
(Ref 7.2.2.)
2.10
(h) . 客户提供的设备、工具和软件确定
(Ref 7.2.2.)
2.11
(l) . 以及所有相关的标准和涉及的程序
2.12
是否有文件规定如何将合同修改的信息通知有关职
(a) .合同要求被充分定义并文件化
(Ref 7.2)
2.5
(b) .合约审查是否用以解決与以前表述不一致的合同或订单的要求,尤其是标准、图面与合同要求不一 致
(Ref 7.2)
2.6
(c).供应商产能满足合同要求
(Ref 7.2.2.)
2.7
(d).产品验收标准和标准的评审
合同评审
QSA Audit Checklist Self Avg Score: Counts: Subtotal: 0% 0 0 Z-DEC Avg Score: Counts: Subtotals: 0% 0 0 Self Z-DEC Score Score 自我評 勤德評 分 分
内部公開
2: 合同评审Contract Review
附件&備注Remarks
(Ref 7.2)
2.1
是否建立了合同评审的流程?
(Ref 7.2.2)
2.2
是否在组织向顾客作出提供产品的承诺之前进行评审?合同审查所引发的措施是否予以记录并加以保 持?
(Ref 7.2.2)
2.3
是否所有类型的订单都按照合同评审程序进行评审?
(Ref 7.2)
该合同评审是否能确保以下内容:

Dell SQ QSA_check listVer3_0

Dell SQ QSA_check listVer3_0

(Ref 8.3, 4.2.4)
(Ref 8.4, 8.5)
(Ref 8.5) (Ref 8.5, 4.2.4)

10.28 Are all corrective actions and results documented?是否所有的纠正措施和结果记录?
Dell Confidential
Nonconformity Control
P2/1
QSA Audit Checklist Does the corrective action request include root cause/containment/short term action? If defect is supplier related, is there any system to feedback to IQC for actions? 10.29 纠正措施是否包括根源请求/控制/短期行动?如果缺陷是供应商的关系,是否有任何反馈系统采取行动,来料质量 控制? Does the corrective action request include long term/preventive action? 10.30 是否有纠正措施的要求,包括长期/预防行动? 10.31 10.32 10.33 10.34 10.35 Is there a system to track status of corrective action requests? 是否有一个系统来跟踪纠正行动请求的状态? Are the contents of the responses/corrective actions appropriate to prevent future occurrences? 是否有回应/适当的纠正措施,以防止日后出现的相同错误? Is the corrective action report reviewed and approved by relevant authorities? 纠正措施报告是否经有关部门审查和批准? Are corrective actions monitored for effectiveness in preventing similar nonconformance? 效能监察是在防止类似的不符合项的纠正措施? Is action taken when progress/implementation of improvement actions is not satisfactory? 是否有采取行动的进展/改善行动的执行情况并不理想?

QSA和QPA基本知识培训资料

QSA和QPA基本知识培训资料

12
QPA 基本知识
QPAA 基本知识
QPA 基本知识
QPA 检查表(SP)
QPA 基本知识
17
审核员的接待:包括车辆安排、会议室安排等 尽可能了解审核组员的信息(包括姓名、职位、人数等)、获取
具体审核安排(审核计划:时间、分组情况、审核范围及目的) 有计划性的带领审核员进行现场审核(做到心中有数、展示好的
QPA 基本知识
QPA检查表包含項目(以Dell客户为例)
序号
1 2 3 4 5 6 7 8 9
QPA 包含项目
Receiving_Warehouse_MRB_Packing (进货-仓库-MRB-包装) Plastic Injection Molding_IMD(注塑) Machining(CNC) Painting(喷涂) Assembly(装配) Integration(综合) Repair Process(返工过程) Metrology(计量) Cleanroom(净房)
Q&A
Hi-P International
QSA&QPA基本知识 培训教材
The
Update: 21th Mar 2011
Integrated
Electro-Mechanics
Solution Provider
1
目录
一、前言 二、QSA&QPA 基本介绍
1、QSA&QPA 定义 2、审核频率及文件来源 3、推动QSA&QPA的目的
QSA 基本知识
QSA 检查表包含项目(以Dell客户为例)
序号
1 2 3 4 5 6 7 8 9 10 11 12
QSA 具体包含项目
Quality Systems(质量系统) Contract Review(合同评审) Design Control (设计控制) Documentation Control(文件控制) Supplier Quality Control(供应商质量控制) Product ID & Lot Traceability (产品标识和可追溯性) Process Control (过程控制) Inspection and Test/Status (检验和测试/状况) Calibration (计量) Nonconforming Product Controlg (不合格品控制) Handling, Packaging, Storage & Delivery(处理、包装、储存和运输) Quality Records (质量记录)

SQE岗位职责

SQE岗位职责

SQE岗位职责sqe工作职责说明1. 推动供应商内部质量改善1.1 推动供应商成立完善的sjqe及qit组织.1.2 供应商制程变更及材质变更的确认管控动作.1.3 新材料及变更材料的管控.1.4 推动厂商导入常用的质量体系如,spc, 6sigma 等品管手法。

1.5 材料质量目标达成状况的改善及检讨。

1.6 不合格项目的改善确认动作。

1.7 材料异常的处理及成效的确认。

2. 推行执行sqm的系统程序文件.2.1 供应商的评监,择优选择厂商。

2.2 供应商的定期及异常稽核的执行。

2.3 供应商的辅导,提升质量。

2.4 执行供应商的奖罚措施。

2.5 建立完善规范的材料作业指导书3. 报表执行3.1 每月的供应商等级评比。

3.1 每年的供应商等级评比。

3.2 供应商mbr, qbr 会议的召开。

3.3 8d report 的发出及时效管控及改善效果的跟进。

3.4 供应商质量月报,fai 报表,信赖性报表的跟催及确认。

sqe供货商管理工程师——(supplier quality engineer)1、必须要有供应商跟踪的方式,质量问题独立处理的方法;2、高级职位必须要有成本控制、质量控制管理的清晰思路与意识、坚持的原则底线;3、供应商的内部品质管理流程、以及可能出现的问题对应方式。

4、稳定性的保证手段。

补充:1、sqe负责保障供应商所供原材料的质量,在进料检验、生产过程检验、客户抱怨等,只要是由于原材料质量缺陷引发的,都要及时反馈供应商要求其改善;2、sqe负责追踪确认供应商的改善报告(8d)及实施效果,必要时可进行现场审核检查;3、sqe负责制定进货检验部门(iqc)的检验规范及检验计划,并适时对检验员进行培训指导;4、sqe可以参与供应商初始样品的评估放行工作;5、sqe每个月或每个季度,对现有供应商的质量状况进行统计评分,对评分较低的供应商提出限期改善要求;6、sqe参与新供应商开发与审核,与采购部门一起对新供应商进行考核打分,确定其是否可以成为合格供应商。

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Dell Confidential Document No. COR.40.WWP.SQ.0003 Rev 3.0Information and InstructionsPURPOSEThis document was developed as an Audit Tool to assess a supplier's Quality Systems against Dell's Quality Systems Requirements.The Dell Quality Systems Audit (QSA) is build upon the ISO-9000 Quality Systems Standard, but with additional Dell specific requirements included.SCOPEThe Dell Quality Systems Audit is not commodity specific, therefore it may be used to assess the Quality Systems deployed by a supplier/manufacture irrespective of the commodity.AUDIT BY SELF ASSESSMENTA supplier's facility is required to complete a self assessment using this tool in advance of the Dell Audit. (One QSA is required per facility.)By doing this, a facility will be able to prepare for the audit and seek advance help and guidance from Dell SQE to be best positioned to succeed.It is expected that during the self-assessment process, that the supplier will use this opportunity to ask questions for either clarification or to better understand intent of the audit criteria. Waiting for the formal Dell audit to ask these types of questions is too late. It is also expected that based on self audit results, a supplier will inform the Dell team of their readiness for a formal Dell audit.A self assessment is completed by scoring the relevant column in each worksheet.AUDIT BY DELLDuring the audit process, the Dell SQE may wish to review every question/criterion listed on the audit document, or alternatively the SQE may choose to focus only on those questions for which the supplier awarded themselves a score of 1 by self-assessment. The path taken is left to SQE discretion.The score awarded by the SQE Auditor will be entered in the 'Score' column on each worksheet.AUDIT RESULTSThe SQE Auditor must complete ALL sections before an Audit Result can be declared.The Audit Result of each section is based on the number of questions scored as 1 versus the total number of questions of the section.Any questions that are scored as N/A are adjusted automatically in the score denominator.The overall average score does not determine the Audit Result, rather all the individual section scores will determine the Audit Result.The 'Pass' score for the Audit is 90%. If the Audit Scores for all sections of equal or greater than 90% are achieved, a 'Pass' or 'Approved' result is awarded.If an Audit Score of equal or greater than 80% but less than 90% is achieved at any section, a 'Conditionally Approved' result is awarded.If an Audit Score of less than 80% is achieved at any section, a 'Fail' or 'Not Approved' result is awarded.If a "Conditionally Approved" Result is awarded, a Corrective Action Plan is due from the supplier within TWO weeks of the date of audit completion for any sections of the QSA that are below 90%.If a "Not Approved" Result is awarded, a Corrective Action Plan is due from the supplier within TWO weeks of the date of audit completion for any sections of the QSA that are below 80%. On completion of this Corrective Action Plan, a supplier is required to generate second Corrective Action Plan to bridge to the 90% 'Approved' Status.All Corrective Action Plans must contain a timeline to 'bridge' to a 'Conditionally Approved' or 'Approved' status, depending on the initial audit result, and must propose a target date for a Dell follow-up Audit.Failure to achieve a 'Conditionally Approved' Result on a follow up Audit may impact business award decisions.A PASS RESULTOnce a supplier's facility has Passed the Audit, the Quality Systems are approved for the facility audited, not all supplier facilities.Passing the QSA does not guarantee a business award, but is the first step towards winning technical approval for a site. In addition, many commodities have a commodity specific Quality Process Audit (QPA), which also requires to be passed before technical approval may be obtained.AUDIT MECHANICS and QUESTIONSThe Audit breaks down the Quality System into individual sections, each of which is represented by an individual worksheet.Within each worksheet is contained a series of questions specifically pertaining to the section being examined.The questions were devised and developed as closed questions with every attempt to avoid ambiguity.Because of the closed nature of the questions, there can only be one of three answers to any question, i.e. Yes (1), No (0), or N/A (x).If the Criterion is fully met, a score of 1 is obtained. If the Criterion is not met, a score of 0 is obtained.A score of N/A (x) may be awarded if the SQE believes that any particular question is truly Not Applicable in the case of the supplier facility under review.In any cases the total number of N/A should be kept as minimum as possible.If there is any doubt as to the score to award for any given Criterion, a score of zero shall be awarded by default.Any Criterion that scores 1 shall be clearly demonstrated, followed, and be beyond reproach.In the event that a supplier clearly meets the intent of the audit question, but does not exactly do what the question asks, a score of 1 shall be given.TRAININGThe QSA is very technical in content with regard to Quality Systems and Engineering Techniques.An internal training session will be provided to the SQEs who use this checklist.SQEs who use this tool are considered within Dell as being sufficiently qualified to conduct this audit.AUDIT SCHEDULEThe Audit may be used as and when the need arises. However, Dell may conduct an official audit annually for key suppliers. The frequencyof the re-audit will be based on the audit result & action closure of the last audit, as well as the supplier quality performance in the past year period.Before conducting an audit, the auditor must ensure the Dell commodity management team responsible for the relationship are advised of the audit schedule.It is also intended for suppliers to conduct internal audits by self assessment every quarter so progress may be reported to Dell.ADDITIONAL QUESTIONSDELL Quality Systems Audit ChecklistCOR.40.WWP.SQ.0003 Rev 3.0Please contact Alfred Lau at alfred_lau@ for additional information.REVISION HISTORYDate Description Of RevisionRevised ByRev.Original document.Pak Chew Ng 1.0Changes to make it generic.Frank Widjaja 1.1Corrected typographical errors, added revision history Robert Yeopage and added header stating revision number.Modified to use for all commodities as the new QSA Audit Tim W. Boyd/ Jill Terry5-May-99(replacing the 135pt audit form) -- changed subject tabs, 2.0numbering, question content, and scoring.14-Dec-01Added tab for Field Services use, Changed final scoring calculation to (total actual score overall/total questions asked)* 100.Karla Sartin/Jeff Scott2.119-Apr-98 1.2Quality System AuditDell Confidential Document No. COR.40.WWP.SQ.0003 Rev 3.0。

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