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上海翻譯公司完成手冊管理英文翻譯
發(fā)布時間：2020-11-30 08:12 點(diǎn)擊：
上海翻譯公司完成手冊管理英文翻譯
Chapter 8 Measurement, Analysis and Improvement1. PurposeIn order to ensure that the products can meet requirements, the company shall supervise, measure, analysis and consistently improve each process during the implementation of every process.2. ScopeEach process of quality system operation in the company3. Content3.1 Supervision and measurement3.1.1 Client satisfactionThe company shall follow the Client Satisfaction Degree Survey Procedures to obtain information on whether the organization has met the client requirements or not.3.1.2 Internal examination and verification3.1.2.1 The company shall, in accordance with Internal Quality Examination and Verification Procedures, review the system operation within regulated time interval, to ensure:a) the compliance with planned arrangement, standard requirements, and the requirements of the organization to the system;b) and receipt of effective implementation and maintenance.3.1.2.2 According to each department operation status, the impact of the status on the system, and the prior examination and verification status, the annual examination and verification can be made. The examination and verification personnel shall guarantee they have no direct relationship with the content to be examined and verified.3.1.2.3 The scope, frequency, personnel and methods of the examination and verification shall follow the Internal Quality Examination and Verification Procedures.3.1.2.4 The record of examination and verification shall be kept. For relevant missing record, improvement measures shall be adopted to follow up and check.3.1.3 Process supervision and measurementThe company shall adopt proper methods to supervise and measure the system process, to prove the capacity of results planned by process realization. When appropriate, the company shall adopt improvement measures to ensure the compliance of the products.3.1.4 Product supervision and measurement3.1.4.1 The company shall, in accordance with the Checkout Procedures during Manufacture Process, Ex-factory Checkout Procedures and Client Acceptance Control Procedures, measure and monitor the product realization process, to verify whether the products meet the requirements.3.1.4.2 The company shall define product release rights and liabilities.3.1.4.3 Unless the products are approved by relevant authorized personnel and the approval of clients, the products cannot be released before completion of each realization process.3.1.5 Supervision, examination and assessment of quality management activities3.1.5.1 The company shall conduct supervision and examination for quality management activities at all management levels, and clearly supervision the duties, frequencies and methods for the examinations. For the problems found in the examinations, the written rectification and reform requirements shall be put forward timely, supervise implementation and verify the results of rectification and reform. The content of rectification and reform include:Important Document Safekeeping No copy is allowed without permission（Form No. Q4002 The 3rd Version）Document No. Q1001The 7th Version, Page 24/27Quality Manual Compiling Department: General Manager OfficeCompiling Date: August 15, 2011a) The implementation of laws, regulations and standards;b) Quality management system and the implementation of supporting documents;c) Implementation of position duties and targets;d) Implementation of rectification and reform requirements.3.1.5.2 The company shall conduct supervision and examination for the quality management activities of the Project Management Department, with the content including:a) Implementation of project quality management planning results;b) Implementation of opinions and rectification and reform requirements put forward by the company, contract-issuing party or supervision party.c) The situation of contract implementation;d) The realization of quality targets.3.2 Control of disqualified productsThe company shall identify and control disqualified products according to the Disqualified Product Control Procedures, to avoid unexpected use or delivery. The company shall also clarify the treatment duties and procedures for disqualified products.3.2.1 Adopt measures to avoid disqualified products.3.2.2 With the approval of relevant authorized personnel or clients, the company can make a concession to use, release or accept disqualified products.3.2.3 Adopt measures to avoid the original expected use or application.3.2.4 Re-examine the products after correction, to improve the products are in line with requirements3.2.5 When the products are found to be disqualified after delivery or during the use process, the company shall adopt measures which are fit to the degree of disqualification impact or potential impact.3.2.6 The disqualification features and the follow-up measure records shall be kept.3.2.7 The responsibility investigation for the disqualified products shall be implemented as per Quality Accident Responsibility Investigation Mechanism.3.3 Data analysis3.3.1 The company shall collect and analysis proper data as per Statistical Technology Control Procedures, to prove the appropriateness and effectiveness of the system, and to assess where the effectiveness of the system can be improved continuously. This shall include the results from supervision and measuring results, and other relevant resource data.3.3.2 Data analysis can cover information of the following perspectives:a) Laws, regulations, standards and rules;b) Client satisfaction degree;c) Required product compliance;d) Process and product performance and trend.e) Suppliers’ status;Important Document Safekeeping No copy is allowed without permission（Form No. Q4002 The 3rd Version）Document No. Q1001The 7th Version, Page 25/27Quality Manual Compiling Department: General Manager OfficeCompiling Date: August 15, 2011f) Requirements from relevant parties of engineering construction on the construction company’s engineering quality and quality management level;g) Engineering quality management situation at all management levels and engineering qualification examination results;h) Construction enterprise quality management supervision and examination results;i) Experience and lessons of other construction enterprises in the same industry;j) Market demand;k) Quality return visit and service information.3.3.3 If data analysis is enough to show abnormalities of system operation, each relevant responsible department shall come up with improvement measures as per Statistical Technology Control Procedures and Correction and Prevention Measure Control Procedures.3.4 Improvement3.4.1 Quality management improvement and innovationThe company shall, in accordance with Statistical Technology Control Procedures and Correction and Prevention Measure Control Procedures, continuously conduct improvement and innovation through quality, quality target, examination and verification results, data analysis, correction and prevention measures and management review.3.4.2 Correction measuresThe company shall, in accordance with Correction and Prevention Measure Control Procedures, diminish disqualification and avoid reoccurrence.3.4.2.1 Determine the disqualified items.3.4.2.2 Judge the reasons for abnormal events.3.4.2.3 Assess improvement measures and prevent the reoccurrence of similar abnormalities.3.4.2.4 Confirm and implement improvement measures.3.4.2.5 Preserve implementation record.3.4.2.6 Assess the effectiveness of measures adopted.3.4.3 Prevention measuresThe company shall, in accordance with Correction and Prevention Measure Control Procedures, determine measures to diminish the reasons of potential disqualifications.3.4.3.1 Determine potential disqualifications and the reasons.3.4.3.2 Assess improvement measures.3.4.3.3 Determine and implement the needed measures.3.4.3.4 Preserve implementation record.3.4.3.5 Assess the effectiveness of measures adopted.4. Reference Documents4.1 Client Satisfaction Degree Management Procedures…………………………………………….No. Q20324.2 Internal Quality Examination and Verification Procedures…………………………………….No. Q2033Important Document Safekeeping No copy is allowed without permission（Form No. Q4002 The 3rd Version）Document No. Q1001The 7th Version, Page 26/27Quality Manual Compiling Department: General Manager OfficeCompiling Date: August 15, 20114.3 Checkout Procedures during Manufacture Process………………………………………………….No. Q20344.4 Ex-factory Checkout Procedures……………………………………………………………….…………….No. Q20354.5 Client Acceptance Control Procedures…………………………………………..………….…………….No. Q20364.6 Disqualified Product Control Procedures……………………………………..………….………………No. Q20374.7 Statistical Technology Control Procedures…………………………………..………….………………No. Q20384.8 Correction and Prevention Measure Control Procedures……………..………….………………No. Q20404.9 Quality Accident Responsibility Investigation Mechanism…………..………….………….……No. Q2036Important Document Safekeeping No copy is allowed without permission（Form No. Q4002 The 3rd Version）世聯(lián)翻譯-讓世界自由溝通！專業(yè)的全球語言翻譯供應(yīng)商，上海翻譯公司專業(yè)品牌。絲路沿線56種語言一站式翻譯與技術(shù)解決方案，專業(yè)英語翻譯、日語翻譯等文檔翻譯、同傳口譯、視頻翻譯、出國外派服務(wù)，加速您的全球交付。 世聯(lián)翻譯公司在北京、上海、深圳等國際交往城市設(shè)有翻譯基地，業(yè)務(wù)覆蓋全國城市。每天有近百萬字節(jié)的信息和貿(mào)易通過世聯(lián)走向全球！積累了大量政商用戶數(shù)據(jù)，翻譯人才庫數(shù)據(jù)，多語種語料庫大數(shù)據(jù)。世聯(lián)品牌和服務(wù)品質(zhì)已得到政務(wù)防務(wù)和國際組織、跨國公司和大中型企業(yè)等近萬用戶的認(rèn)可。- 上一篇：上海翻譯公司完成公司管理類中文翻譯
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