ISO9001:2015质量手册英文版(按标准条款)
新版ISO9001质量手册 2015版
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质量手册QUALITY MANUAL(依据GB/T19001-2015 idt ISO9001:2015标准)文件编号:QM01--2016审核:批准:受控状态:发布日期:2016年7月12日实施日期:2016年7月12日总目录0批准令0.1发布令0。
2任命书1范围2引用标准和术语2。
1引用标准2.2通用术语和定义2.3专用术语3概况3。
1公司概况3.2手册管理4 公司的背景4.1 理解公司及其背景4。
2 理解相关方的需求和期望4.3 质量管理体系范围的确定4.4 质量管理体系及其过程5 领导作用5.1 领导作用和承诺5.2 质量方针5.3 公司的角色、职责和权限6 策划6.1 风险和机遇的应对措施6.3 变更的策划7 支持7.1 资源7。
2 能力7.3 意识7.4 沟通7。
5 形成文件的信息8 运行8.1 运行的策划和控制8。
2产品和服务的要求8.3 产品和服务的设计和开发8.4 外部提供过程、产品和服务的控制8.5 生产和服务的提供8.6 产品和服务放行8。
7 不合格输出的控制9 绩效评价9.1 监视、测量、分析和评价9.2 内部审核9。
3 管理评审10 持续改进10。
1 总则10.2不合格和纠正措施10.2 持续改进11 附录:附录1:生产工艺流程图0 批准令0。
1发布令为规范公司行为,保证产品质量满足顾客和法定要求,提高公司信誉和产品竞争能力,增强顾客满意,公司建立了系统化、文件化的质量管理体系。
该体系符合GB/T19001-2015 idt ISO9001:2015标准的要求,编制了《质量手册》,规定了质量管理体系的组织结构、管理职责和质量管理体系过程的控制要求。
根据公司发展和管理提升的需要,结合2015版标准等要求,经领导层决策,发布本《质量手册》。
《质量手册》阐述了我公司新阶段的质量方针和质量目标,是实施、保持公司质量管理体系的纲领性文件和进行质量管理的公司法规,也是向顾客提供质量保证的证实文件,并作为第三方质量管理体系认证的依据,要求全体员工必须严格贯彻执行。
ISO9001:2015全套文件英文版(含质量手册及全套程序文件)
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Ningbo XXX Material TechnologyCo.,LtdISO9001:2015 Quality ManualRevision [A/0] - [2018/3/1](c) [Copyright Year Of 2018] [Ningbo XXX Material Technology Co.,Ltd]; all rights reserved. This document may contain proprietary information and may only be released to third parties with approval of management. Document is uncontrolled unless otherwise marked; uncontrolled documents are not subject to update notification.Revision [A/0] - [2018/3/1]Page 1 of 19TABLE OF CONTENTS0.0 Revision History and Approval ...................................................................................................................... 3 1.0 Welcome to Ningbo XXX Material Technology Co.,Ltd ................................................................................ 4 2.0 XXX Material: Who We Are ........................................................................................................................... 4 2.1 Determining Our Strategic Direction ......................................................................................................... 4 2.2 Scope of the Management System ........................................................................................................... 4 2.2.1 Scope Statement ............................................................................................................................... 4 2.2.2 Facilities Within the Scope ................................................................................................................ 4 2.2.3 Permissible Exclusions ..................................................................................................................... 5 2.2.4 Scope of the ISO9001:2015 Quality Manual ..................................................................................... 5 3.0 Quality Policy................................................................................................................................................. 5 4.0 Management System Structure and Controls ............................................................................................... 5 4.1 Process Approach .................................................................................................................................... 5 4.1.1 Process Identification ........................................................................................................................ 5 4.1.2 Process Controls & Objectives .......................................................................................................... 6 4.1.3 Outsourced Processes ...................................................................................................................... 7 4.2 Documentation & Records ....................................................................................................................... 7 4.2.1 General .............................................................................................................................................. 7 4.2.2 Control of Documents ....................................................................................................................... 7 4.2.3 Control of Records ............................................................................................................................ 7 4.3 Change Management ................................................................................................................................ 8 4.4 Risks and Opportunities ............................................................................................................................ 8 5.0 Management & Leadership ........................................................................................................................... 8 5.1 Management Leadership and Commitment .............................................................................................. 8 5.2 Customer Focus ........................................................................................................................................ 9 5.3 Quality Policy ............................................................................................................................................. 9 5.4 Organizational Roles Responsibilities & Authorities ................................................................................. 9 5.5 Internal Communication ............................................................................................................................ 9 5.6 Management Review .............................................................................................................................. 10 6.0 Resources ................................................................................................................................................... 10 6.1 Provision of Resources ........................................................................................................................... 10 6.2 Human Resources .................................................................................................................................. 10 6.3 Infrastructure ........................................................................................................................................... 11 6.4 Work Environment ................................................................................................................................... 11 6.5 Organizational Knowledge ...................................................................................................................... 11 7.0 Operation ..................................................................................................................................................... 11 7.1 Operational Planning and Control ........................................................................................................... 12 7.2 Customer-Related Activities .................................................................................................................... 12 7.2.1 Capture of Customer Requirements ............................................................................................... 12 7.2.2 Review of Customer Requirements ................................................................................................ 12 7.2.3 Customer Communication ............................................................................................................... 12 7.3 Design and Development ........................................................................................................................ 13 7.4 Purchasing .............................................................................................................................................. 13 7.5 Provision of [Production of adhesive tape] .............................................................................................. 13 7.5.1 Control of Provision of [Production of adhesive tape] ..................................................................... 13 7.5.2 Identification and Traceability .......................................................................................................... 14 7.5.3 Property Belonging to Third Parties ................................................................................................ 14 7.5.4 Preservation .................................................................................................................................... 14 7.5.5 Post-Delivery Activities .................................................................................................................... 14 7.5.6 Process Change Control ................................................................................................................. 15 7.5.7 Measurement and Release of [Production of adhesive tape] ......................................................... 15 7.5.8 Control of Nonconforming Outputs .. (15)Revision [A/0] - [2018/3/1]Page 2 of 198.0 Improvement ............................................................................................................................................... 15 8.1 General .................................................................................................................................................... 15 8.2 Customer Satisfaction ............................................................................................................................. 15 8.3 Internal Audit ........................................................................................................................................... 16 8.4 Corrective and Preventive Action ............................................................................................................ 16 Appendix A: Overall Process Sequence & Interaction ........................................................................................ 17 Appendix B: ISO 9001:2015 Cross Reference . (18)Revision [A/0] - [2018/3/1] 0.0 Revision History and ApprovalRev. Nature of changes Approval DateA/0 Original release. XXX 2018/3/1Page 3 of 19Revision [A/0] - [2018/3/1] 1.0 Welcome to Ningbo XXX Material Technology Co.,LtdNingbo XXX Material Technology Co., Ltd. Was established in 2000, with the UAE businessmen to build the joint venture company; 2004 Ming Shan founded Nissin special adhesive tape and adhesive tape company; 2008 due to the strategic adjustment of 3 company merger and reorganization, the establishment of Ningbo letter mountains adhesive products Manufacturing Co., Ltd..PVC insulation tape is one of China’s national standard drafting unit, the field of adhesive products governing unit of China, Ningbo, adhesives and related products Industry Association, honorary president of the unit.We produce more than 1000 varieties of products of 11 categories. The annual throughput more than 100,000,000 square of the adhesive and 10,000 ton of the adhesive.Our company located in Ningbo which the city of the east China sea, beside 500 kilometers of shanghai, 20 kilometers from Ningbo list airport and 50 kilograms of the Ningbo seaport. The transport is very convenient (Easy to ship to everywhere on the world).2.0 XXX Material: Who We Are2.1 Determining Our Strategic DirectionXXX Material has reviewed and analyzed key aspects of itself and its stakeholders to determine the strategic direction of the company. This involves:∙Understanding our core products and services, and scope of management system (see 2.2 below).∙Identifying “interested parties” (stakeholders) who receive our [Production of adhesive tape], or who may be impacted by them, or those parties who may otherwise have a significant interest in our company. These parties are identified in the document [Requirements and expectations list of interested parties].∙Understanding internal and external issues that are of concern to XXX Material and its interested parties; also identified in the document [Requirements and expectations list of interested parties]. Many such issues are identified through an analysis of risks facing either XXX Material or the interested parties. Such issues are monitored and updated as appropriate, and discussed as part of management reviews.This information is then used by senior management to determine the company’s strategic direction. This is defined in records of management review, and periodically updated as conditions and situations change.2.2 Scope of the Management System2.2.1 Scope StatementBased on an analysis of the above issues of concern, interests of stakeholders, and in consideration of its products and services, XXX Material has determined the scope of the management system as follows:Production of adhesive tapePage 4 of 19Revision [A/0] - [2018/3/1]Page 5 of 192.2.2 Facilities Within the ScopeThe quality system applies to all processes, activities and employees within the company. The facility is located at: Factory Add :XXX Tel :XXX Fax :XXX XXX XXX2.2.3 Permissible ExclusionsThe following clauses of ISO 9001 were determined to be not applicable to XXX Material.∙ 8.3 Design and development of products and services 2.2.4Scope of the ISO9001:2015 Quality ManualThis manual is prepared for the purpose of defining the company’s interpretations of the ISO 9001:2015 international standard, as well as to demonstrate how the company complies with that standard.This manual does not follow the numbering structure of ISO 9001. Instead, Appendix B presents a cross reference between the sections of this manual and the clauses of ISO 9001:2015.This manual presents “Notes” which are used to define how XXX Material has tailored its management system to suit its purposes. These are intended to clarify implementation approaches and interpretations for concepts which are not otherwise clearly defined in ISO 9001:2015. Notes appear in italics, with gray background.Where subordinate or supporting documentation is reference in this manual, these are indicated by bold italics .∙ Quality PolicyThe Quality Policy of XXX Material is as follows:Quality first, customer satisfaction;Scientific management, continuous improvement. ∙ Management SystemStructure and Controls 4.1Process Approach4.1.1 Process IdentificationXXX Material has adopted a process approach for its management system. By identifying thetop-level processes within the company, and then managing each of these discretely, this reduces the potential for nonconforming [Production of adhesive tape] discovered during final processes or after delivery. Instead, nonconformities and risks are identified in real time, by actions taken within each of the top-level processes.Note: not all activities are considered “processes” – the term “process” in this context indicates the activity has been elevated to a higher level of control and management oversight.The controls indicated herein are applicable only to the top-level processes identified.。
ISO9001质量手册英文版
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ISO9001 Quality Manual (English Version)1. IntroductionThe ISO9001 Quality Manual serves as a primary document that outlines the quality management system (QMS) followed by the organization. It provides guidelines and procedures for achieving and mntning the desired quality standards set by the International Organization for Standardization (ISO). This manual acts as a reference document for employees, customers, audit teams, and other stakeholders to ensure consistent adherence to quality processes.2. ScopeThe scope of this QMS covers all aspects of the organization’s activities, including design, development, production, and service delivery. It includes all departments, functions, and levels within theorganization, ensuring that quality is consistently mntned across the company.3. Document ControlThe organization is committed to mntning an efficient document control system to ensure the validity, accessibility, and integrity of all quality-related documents. This system includes procedures for document creation, revision, approval, distribution, and archival. This document control system ensures that the most current version of relevant documents is readily avlable to all employees.4. Quality PolicyThe organization’s quality policy reflects its commitment to deliver products and services that meet or exceed customer expectations. The quality policy statement emphasizes the organization’s dedication to continuous improvement and compliance with all applicable legal andregulatory requirements. The policy acts as a framework for establishing and reviewing quality objectives to drive long-term success.5. Organizational StructureThe organization is structured in a way that supports effective quality management. Clear lines of responsibility and authority are defined to ensure accountability at all levels. The organizational structure fosters collaboration, communication, and coordination among departments to achieve quality objectives.6. Risk ManagementThe organization recognizes the importance of identifying, assessing, and managing risks that could impact the quality of its products and services. A systematic approach is adopted to analyze potential risks, develop mitigation strategies, and monitor risk levels to proactively address any potential quality issues.7. Resource ManagementThe organization ensures that adequate resources, both human and physical, are allocated to support the implementation and mntenance of the QMS. This includes trning employees to improve their knowledge and skills, providing necessary infrastructure and equipment, and fostering a favorable work environment that promotes quality.8. Product RealizationThe organization follows a well-defined process to ensure consistent quality during the realization of its products and services. This process includes product design, development, sourcing of materials, production, testing, and delivery. Regular quality checks and audits are conducted at each stage to ensure conformity to specifications and standards.9. Measurement, Analysis, and ImprovementThe organization emphasizes the importance of measuring and analyzing performance to drive continuous improvement. Keyperformance indicators (KPIs) are established and monitored to evaluate the effectiveness of the QMS. Non-conformities and customer feedback are analyzed to identify areas of improvement and implement corrective actions to enhance quality.10. Internal AuditsRegular internal audits are conducted to assess the effectiveness of the QMS and ensure compliance with ISO9001 standards. Trned auditors review processes, procedures, and records to identify any gaps or non-compliance. Audit findings are documented, and appropriate corrective actions are initiated to address any identified issues.11. Management ReviewTop management conducts regular management reviews to evaluate the performance of the QMS. These reviews provide an opportunity to assess the suitability, adequacy, and effectiveness of the QMS, as well as to identify opportunities for improvement. Management reviewmeetings play a crucial role in decision-making and setting future quality objectives.12. Continual ImprovementThe organization is committed to continually improving its QMS to enhance customer satisfaction and meet evolving market demands. Lessons learned from internal audits, customer feedback, and performance analysis are used to identify areas for improvement. Process enhancements, employee trning, and innovation are encouraged to ensure the organization remns at the forefront of quality management.ConclusionThis ISO9001 Quality Manual outlines the organization’s commitment to quality and provides a comprehensive guide for implementing and mntning a robust QMS. The document emphasizes the importance of continuous improvement, risk management, andresource allocation to achieve the desired quality standards. By adhering to the principles outlined in this manual, the organization can consistently deliver products and services that meet customer expectations and drive long-term success.Note: This ISO9001 Quality Manual is not intended to be a standalone document. It should be used in conjunction with other relevant procedures and work instructions to ensure the effective implementation of the QMS.。
2015版ISO9001最新换版质量手册详解
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2015版ISO9001最新换版质量手册详解简介ISO 9001是一个国际标准,制定的是质量管理体系的要求。
该标准由国际标准化组织(ISO)制定。
ISO 9001的标准已经更新于2015年。
本文档将详细介绍2015版ISO 9001最新换版质量手册的主要内容,并解释如何适应这些更改。
2015版ISO 9001标准概述2015版ISO 9001标准是ISO 9001质量管理体系全球标准的最新版本,它对2008年版进行了大规模的变更。
新标准的重点是。
为什么如此做。
ISO 9001标准的目标是协助企业监控所有过程,以确保产品或服务的质量符合客户的期望,从而提高客户满意度。
2015版ISO 9001标准的重点是让企业能够具备更大的灵活性,尤其是在非常严格的要求下,众多企业都无法满足ISO 9001标准的严格性,因此,新标准强化了企业的连续改进和风险管理。
持续改进在2015版ISO 9001标准中,持续改进被赋予更大的重要性,该标准通过增加改进要求的条款和增加监控要求的条款来实现这一点。
风险管理在2015版ISO 9001标准中,风险管理被赋予了更大的重要性,该标准要求企业必须考虑所有的风险和机会,并根据风险等级分别采取相应的措施。
ISO 9001质量手册ISO 9001质量手册是质量管理体系的重要组成部分。
它包含所有组成质量管理体系的要素。
概要2015年版的ISO质量管理手册是质量管理体系的重要组成部分。
该文件包含预防性和纠正性的行动以及审核和分析机制,以保证制定的质量策略符合客户的要求。
内容ISO 9001质量管理手册的内容包括以下方面:1.公司质量管理结构2.公司关键过程的描述3.公司的质量管理体系4.公司主要产品和服务的描述,和相关的质量要求5.质量体系的规划、实施、验证、其他支持性流程的描述6.对质量业绩的评估过程7.质量管理的持续改进措施8.公司质量政策和目标结论ISO 9001质量手册是一个企业的质量管理体系的重要组成部分。
ISO9001:2015版质量管理手册范本
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本公司《质量手册》是本公司质量管理体系纲领性文件和行动准则,适用于公司各职能部门的质量管理过程。现批准《质量手册》自年月日实施。
我要求公司全体员工必须认真学习《质量手册》,正确理解,履行职责,贯彻落实各项规定要求,保证质量管理体系持续有效运行,以实现公司的质量安全方针和质量安全目标。
质量目标及其实施的策划
最高管理者应确保以质量方针为基础建立本公司的质量目标,并
在质量方针给定的框架内在各部门进行展开;
质量目标应满足方针要求:
包括满足产品、服务和顾客满意要求所需的内容;
能够测量,可作为质量管理体系评价的依据;
在组织内充分沟通并理解。
在必要时对目标进行更新,如:目标已经实现、组织经营方针发生变化、相关方要求变化等。
为所识别出来的过程规定运行准则,并进行监视和测量,对绩效指标进行分析,确保过程按预期要求运行,同时为改进提供依据;
)确保过程所需资源和信息的获得;
)实施过程策划的控制措施,并对过程进行监控,确保实施符合策划的要求;
在对过程分析的基础上,针对要求进行必要的变更,以确保过程持续符合期望的结果;
)持续改进这些过程。
产品和服务要求的确定
产品和服务要求的评审
产品和服务要求的更改
产品和服务的设计和开发
总则
设计和开发策划
设计和开发输入
设计和开发控制
设计和开发输出
设计和开发更改
外部提供的过程、产品和服务的控制
总则
控制类型和程度
提供给外部供方的信息
生产和服务提供
生产和服务提供的控制
标识和可追溯性
ISO9001-2015-标准中英文
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ISO 9001:2015Quality management systems —Requirements质量管理体系-要求Introduction引言0.1 General 总则The adoption of a quality management system is a strategic decision for an organization that can helpto improve its overall performance and provide a sound basis for sustainable development initiatives.The potential benefits to an organization of implementing a quality management system based on this International Standard are:a) the ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements;b) facilitating opportunities to enhance customer satisfaction;c) addressing risks and opportunities associated with its context and objectives;d) the ability to demonstrate conformity to specified quality management system requirements。
This International Standard can be used by internal and external parties。
ISO9001;2015版质量手册
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质量手册(A/0版)主编:审核:批准:编号:2020-4-1发布2020-4-1实施XX有限公司0.0更改一览表0.1 发布令依据公司要求,ISO9001:2015标准而成的《质量管理体系文件》经公司审定,今天发布,定于2020年4月1日正式实施。
产品质量和服务质量是我公司赖以生存和发展的生命线,是管理水平与人员素质的集中体现。
《质量管理体系文件》是我公司对顾客的承诺,也是我公司员工必须严格遵照执行的规范性文件。
公司的质量管理工作必须完全按照本文件所规定的内容实施,任何人不得违反。
总经理:2020年4月1日文件编制、评审会签记录总经理:日期:0.2 目录0.3公司简介0.4 质量方针质量目标质量方针:精心制造、顾客满意、管理创新、持续改进。
1、精心制造:以精益求精的服务精神,精心管理、精选材料、精益生产、不断改进、做出更优质的产品,为客户提供更好的服务,赢得客户持久的信赖。
力求精准、实现零缺陷,提升为客户服务的附加价值,是恒瑞追求品质卓越的至高境界!2、顾客满意:保证持续的客户满意是我们的永恒追求,及时、准确调查与分析客户的需求并满足之,做到不断的持续改善。
全公司树立一切始终服务于顾客的意识,对内,上道工序完全服务于下道工序,下道工序是上道工序的顾客,每道工序的员工接受下道工序的抱怨并改善,从而达到全员追求持续的“顾客满意”。
3、管理创新:专业化的高压清洗产品技术、工艺技术及生产技术是我们恒瑞公司生存的基础与核心,因此我们要在技术上必须保持专业领先,就务必在技术、工艺及管理等方面始终不渝地坚持创新,这也是我们能服务于客户的核心价值所在。
4、持续改进:在现有的标准、现有的管理基础上我们不满足现状,以更高的要求为标杆,积极找出差距,在产品、技术、工艺及管理等方面寻求不断的修正、完善和创新,建立合理改进机制,确保质量管理处于不断持续改进的良性轨道。
质量目标:①顾客满意度95分以上②出货交期达成率90%③成品出货合格率98%以上④客户重大投诉率每年为零⑤物料异常损耗率3‰⑥重大安全事故为零。
ISO9001质量手册英文版
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ISO9001质量手册英文版WOLSTENHOLME INTERNATIONAL LIMITEDCONTENTS1.0 Scope of the Quality Management System at Wolstenholme Internatio nal Limited1.1 Statement of Quality Policy2.0 Quality Management System Documented Procedures2.1 Document Control2.2 Control of Quality Records2.3 Internal Quality Audits2.4 Control of Nonconforming Product2.5 Corrective Action2.6 Preventative Action3.0 Quality Management System Processes and Interrelations 3.1 Organisation Charts3.2 Responsibilities3.3 Interrelation of Processes3.4 Processes1.0 Scope of the Quality Management System at Wolstenholme International LimitedWolstenholme International Limited is a Company with a long-standing succe ssful history of supplying metal powders, pastes, pellets, varnish, offset ink, flexog raphy ink and other related products for use in a large range of applications, on a w orldwide basis. The scope of the Quality Management System encompasses all acti vities on the Darwen Site.The Metallic Powders Operation at Darwen is responsible for the manufacture and supply of metal powders and pigments mainly in aluminium, copper and brass (bronze) based alloys, for use in printing, inks, plastics and other industrial and eng ineering applications.The Ink Operation at Darwen is responsible for the manufacture of a wide ran ge and type of printing ink, 'one-pack' gold ink, varnish and related printing produc ts.All production processes at Darwen are validated before leaving the site and a s such sub-clause 7.5.2 is excluded.The overall operation at Darwen is controlled by the Ink & Print business unit and the Industrial business unit.Technical Service and Research and Development are vital to the future devel opment of the Company, together with understanding and developing new products and applications for our customers.The manufacturing, technical and administration functions of the Company ar e based in Darwen, Lancashire, England and employ some 210 staff at that locatio n.Through the application of Quality Management Systems and Company wide t raining programmes, Wolstenholme International Ltd. is committed to ensuring con tinuous improvements to both its processes and product technology.WOLSTENHOLME INTERNATIONAL LTD.QUALITY POLICYWolstenholme International Limited is committed to the provision of customer satisfaction. Quality in everything we do is the central ingredient in the above com mitment. Our commitment goes beyond maintaining a quality system which fully c omplies with the requirements of BS-EN-ISO 9001. We are committed to achievin g, maintaining and improving overall organisational performance and capabilities b y the application of the principles outlined in BS-EN-ISO 9004:2000We will maintain and continuously improve our quality management system b y the setting of measurable quality objectives throughout the organisation and vigo rous internal audits. We will review our performance at regular management review s. Additional inputs to these reviews will also include customer feedback, process p erformance and product conformance. The prime output of the review will be to ens ure continuing customer satisfaction and improvement of products.As part of this commitment we will identify and meet the training needs of our employees, so ensuring that the needs of our customers are met. This Policy will b e made available throughout our organisation to ensure that the commitment to our customers is clear and widely understood.Chris Ravenscroft Managing DirectorControl of Quality RecordsAll quality records will be maintained and controlled. The records will be legi ble and stored in such a manner as to protect them from damage, loss and deteriorat ion. Quality records will also be stored and clearly located in such a manner as to fa cilitate easy retrieval of information.REF: Control of Quality/ Environmental Records - WIQSP.22.3 Internal Quality AuditsInternal audits will be carried out in accordance with Company procedures and will be conducted for any of the following reasons:-(i) On a scheduled basis.(ii)2.5 Corrective Actiontomers have cause to complain or following in-progress/ final inspection. Correctiv e action requests may also be raised in an effort to improve current working practis es. Corrective actions and customer complaints will be reviewed at Management R eview Meetings.When non-conforming products or services are identified, the root cause of the problem will be investigated, corrective action taken and preventative measures ini tiated to preclude a recurrence.REF: Corrective Action - WIQSP.52.6 Preventative ActionCorrective action is taken as a result of Product or process nonconformity. It is hence a reactive measure and does not necessarily prevent further non conformancThe SARA Manager (MR) has the primary responsibility to structure the qual ity system which will involve all sections and also to ensure compliance with all qu ality system requirements.Specifically, the Management Representative is involved in areas such as:-- Drafting the policy on quality assurance of the Company along with th e Operations Director.- Setting the quality management objectives of the Company.- Reporting on the performance of the Quality System at Management Review Meetings.- Determining and reporting the principle causes of quality system non-c onformances.- Monitoring the quality system to determine where improvements are needed and monitoring the necessary corrective action.- Maintain contact with the external Registration Body on matters relating to t he operation of the Quality System.SARA Manager is responsible to the Operations Director for the upkeep and maintenance of all the ISO Systems and the Company Health and Safety Policy. Th e SARA Manager is also responsible for driving the E,H&S policies within the Co mpany.Technical DirectorsThe Technical Directors for pigments and inks are responsible to the Managin g Director .. and ink and print Director respectively for ensuring that processes and equipment are designed and developed such that product of the highest attainable q uality is produced consistently and efficiently.Human Resources and Administration ManagerThe Human Resources and Administration Manager reports to the Managing Director and is responsible for managing all aspects of the personnel function, whic h includes the facilitating, co-ordinating, recording personnel issues and training, w ithin Wolstenholme International Ltd.Ink Manufacturing ManagerThe Ink Manufacturing Manager is responsible to the Operations Director for t he control of stocks, manpower and the process necessary to produce products to th e correct specification within a given time.Sales DirectorsThe Sales Directors are responsible to the Managing Director for ensuring that customers' requirements for the sale of printing/ industrial powders, pastes, pellets, inks, varnishes and related Company products are taken, reviewed and dealt with e fficiently.UK Financial Controller and Purchasing Manager.The UK Financial Controller & Purchasing Manager is responsible to the Fina ncial Director for the effective control and reporting of manufacturing costs incurre d by the manufacturing facility at the Darwen site.There is also a responsibility to the Financial Director for the effective and eco nomic procurement of raw materials and consumables used in the business of the C ompany.Research and Development ManagersResearch and Development Managers are responsible to Technical Directors f or managing Research and Development projects, maintaining customer contact du ring the project development stages and the general running of research laboratorie s.Bronze Manufacturing Manager / Offset Ink R&D ManagerThe Bronze Manufacturing Manager and Offset Ink R&D Manager (ink operat ions) are responsible to the Technical Directors for the agreement of specifications with the customer, and ensuring that there is a facility to continuously monitor and i nspect the product to ensure that all such requirements are met.Customer Services ManagerThe Customer Services Manager is responsible to the Operations Director for t he operation of Customer Services together with a team of administrators.Production Supervision。
ISO9001:2015版质量手册(完整)【范本模板】
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*本文件盖有红色“受控"印章时方为受控文件技有限责任公司实施日期2018年01月01日二方审核和第三方认证审核.b)各种内部和外部因素,具体见SWOT分析表;c)各相关方(包括客户、供应商、员工和政府等部门)对企业没有特别要求,属于正常的要求,都满足这些要求,已经转化为内部文件执行;4.4 质量管理体系及其过程4.4.1.识别顾客及法律、法规要求,依据本公司产品确定为达到质量目标所需的过程。
4。
4.2。
分析、确定各输入及输出过程顺序及相互关系。
4.4。
3。
明确所使用的资源、职责并确定过程的程序。
4.4.4。
确定体系进行的目标及运行方法与测量监视方法。
4。
4.5.建立和保持所需的指导书、规范标准、和记录。
4.4.6.实施和保持作业程序,使体系正常运行.4.4。
7。
通过对各流程的监视量测和分析的结果,对资料进行分析与利用、评价体系的有效性,并进行体系改进。
4.4。
8.策划和实施并评价改进效果.4。
4。
9.在过程当中建立6.1所识别的要求确定公司存在的风险和机会的措施。
4。
4。
10。
通过对管理体系的策划,确定本公司所要控制的过程和过程间的相互关系及其在管理体系中的作用(详见过程模式关系图)。
我司将过程分为:顾客导向过程(COP),支持过程(SP),管理过程(MP),并进行识别,以确保顾客导向过程(COP)对客户的满意程度的有效性.(详见过程策划一览表〈附件三>和质量管理体系过程关系图〈附件五〉).4.4.11本公司QMS的基本框架如下图所示:技有限责任公司实施日期2018年01月01日附件五:质量管理体系过程关系图附件六:文件清单技有限责任公司实施日期2018年01月01日附件六:质量管理体系品质流程图。
ISO9001 2015 标准条款
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ISO9001:2015标准条款前言1 范围2 规范性引用文件3 术语和定义4 组织的背景4.1 理解组织及其背景4.2 理解相关方的需求和期望4.3 质量管理体系范围的确定4.4 质量管理体系5 领导作用5.1 领导作用和承诺5.2 质量方针5.3 组织的作用、职责和权限6 策划6.1 风险和机遇的应对措施6.2 质量目标及其实施的策划6.3 变更的策划7 支持7.1 资源7.2 能力7.3 意识7.4 沟通7.5 形成文件的信息8 运行8.1 运行的策划和控制8.2 市场需求的确定和顾客沟通8.3 运行策划过程8.4 外部供应产品和服务的控制8.5 产品和服务开发8.6 产品生产和服务提供8.7 产品和服务放行8.8 不合格产品和服务9 绩效评价9.1 监视、测量、分析和评价9.2 内部审核9.3 管理评审10 持续改进10.1 不符合和纠正措施10.2 改进质量管理体系-要求1 范围本标准为有下列需求的组织规定了质量管理体系要求:a)需要证实其具有稳定地提供满足顾客要求和适用法律法规要求的产品和服务的能力;b)通过体系的的有效应用,包括体系持续改进的过程,以及保证符合顾客和适用的法律法规要求,旨在增强顾客满意。
注1:在本标准一中,术语“产品”仅适用于:a) 预期提供给顾客或顾客所要求的商品和服务;b) 运行过程所产生的任何预期输出。
注2:法律法规要求可称作为法定要求。
2 规范性引用文件下列文件中的条款通过本标准的引用而构成本标准的条款。
凡是注日期的引用文件,只有引用的版本适用。
凡是不注日期的引用文件,其最新版本(包括任何修订)适用于本标准。
ISO9000:2009 质量管理体系基础和术语3 术语和定义本标准采用 GB/T19000 中所确立的术语和定义。
4 组织的背景环境4.1 理解组织及其背景环境组织应确定外部和内部那些与组织的宗旨、战略方向有关、影响质量管理体系实现预期结果的能力的事务。
2015版ISO9001质量管理体系新旧标准条款对应及新标准主要变化点(供参考)
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8.3.2 设计和开发策划
7.3.1 设计和开发策划
确定设计和开发的各阶段及其控制时,组织应考虑:(新增的) 1.产品和服务的设计和开发所需的内部和外部资源 2.顾客和使用者参与设计和开发过程的需求 3.证实已经满足设计和开发要求所需的形成文件的信息
8.3.3 设计和开发输入
7.3.2 设计和开发输入 7.3.4 设计和开发评审 7.3.5 设计和开发验证 7.3.6 设计和开发确认
8.4 外部提供过程、产品 和服务的控制
8.4.1 总则
4.1 总要求 7.4.1 采购过程
8.4.2 控制类型和程度 8.4.3 外部供方的信息 8.5 生产和服务提供
7.4.1 采购过程 7.4.3 采购产品的验证 7.4.2 采购信息
7.5.1 生产和服务提供的控 8.5.1 生产和服务提供的 制 控制 7.5.2 生产和服务提供的过 程确认
4.2 理解相关方的需求和 新增 期望 4.3 确定质量管理体系的 1.2 应用 范围 4.2.2 质量手册
4.4 质量管理体系及其过 4.1 总要求 程 5 领导作用 5.1 管理承诺 5.2 以顾客为关注焦点
1.过程方法指理解需求,寻求最佳方式实现需求,检查需求是否被满 修订一体化管理手册的相 足,是否以最佳方式完成 2.增加了规定与过程有关的职责和权限,应注意理解过程所有者的职 关内容 责
6.3 变更的策划
5.4.2 质量管理体系策划
1.变更策划的时机:1)QMS建立、实施的初始阶段;2)组织结构发生 调整、生产工艺发生重大变化,组织的现有的QMS需要变化和更新 时,组织根据变更对QMS符合性和完整性的影响,确定所需措施和实 修订一体化管理手册的相 施策划;3)为满足新要求,调整充实现存的QMS时;4)诸多管理体 关内容 集成或一体化时。 2.强调变更前的评审
2015年正式版_质量手册(ISO9001-2015年)
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XX有限公司质量手册QUALITY MANUAL(符合GB/T19001-2015 idt ISO9001:2015标准)---QM---2016版本: C修改码: 0受控号:编制:办公室(2015年12月3日)审核:(2015年12月3日)批准:(2015年12月3日)2015年12月3日发布 2016年1月1日实施发布令为规范公司行为,保证产品质量满足顾客要求,提高公司信誉和产品竞争能力,使质量管理与国际惯例接轨,本公司建立了系统化、文件化的质量管理体系。
该体系符合GB/T19001-2015 idt ISO9001:2015标准的要求,编制了C版《质量手册》,规定了质量管理体系的组织结构、管理职责和质量管理体系过程的控制要求。
根据公司发展和管理提升的需要,结合2015版标准转换,经领导层决策,对现版文件换版,发布了C版《质量手册》。
C版《质量手册》阐述了我公司新阶段的质量方针和质量目标,是实施、保持公司质量管理体系的纲领性文件和进行质量管理的公司法规,也是向顾客提供质量保证的证实文件,并作为第三方质量管理体系认证的依据,要求全体员工必须严格贯彻执行。
从二0一六年一月一日起实施。
特批准发布2015年12月3日任命书为了贯彻执行GB/T19001-2015 idt ISO9001:2015标准的要求,加强对质量管理体系的管理,特任命同志为本组织的管理者代表。
管理者代表的职责是:a)确保质量管理体系符合标准的要求;b)确保各过程获得其预期输出;c)报告质量管理体系的绩效及其改进机会,特别向最高管理者报告;d)确保在整个组织推动以顾客为关注焦点;e)确保在策划和实施质量管理体系变更时保持其完整性。
总经理:2015年12月3日我公司为保证产品质量始终得到顾客的满意,经管理者代表组织员工按总经理对方针、目标的要求,进行了讨论,形成了公司的质量方针和目标,并经过了总经理批准。
现声明如下:1.质量方针:诚信为本以质量求生存科技创新追求行业领先水平在质量管理中,我公司认真按照GB/T19001-2015 idt ISO9001:2015《质量管理体系要求》进行质量管理,生产中严格按照顾客要求和产品标准进行生产,诚信为本,科技创新,生产出顾客满意的高附加值的机械产品。
ISO9001:2015版质量手册(完整)
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*本文件盖有红色“受控”印章时方为受控文件
限责任公司实施日期2018年01月01日4.4 质量管理体系及其过程
4.4.1.识别顾客及法律、法规要求,依据本公司产品确定为达到质量目标所需的过程。
4.4.2.分析、确定各输入及输出过程顺序及相互关系。
4.4.3.明确所使用的资源、职责并确定过程的程序。
4.4.4.确定体系进行的目标及运行方法与测量监视方法。
4.4.
5.建立和保持所需的指导书、规范标准、和记录。
4.4.6.实施和保持作业程序,使体系正常运行。
4.4.7.通过对各流程的监视量测和分析的结果,对资料进行分析与利用、评价体系的有效
性,并进行体系改进。
4.4.8.策划和实施并评价改进效果。
4.4.9.在过程当中建立6.1所识别的要求确定公司存在的风险和机会的措施。
4.4.10.通过对管理体系的策划,确定本公司所要控制的过程和过程间的相互关系及其在
管理体系中的作用 (详见过程模式关系图) 。
我司将过程分为:顾客导向过程
(COP),支持过程(SP),管理过程(MP),并进行识别,以确保顾客导向过程(COP)对
客户的满意程度的有效性.( 详见过程策划一览表<附件三>和质量管理体系过程
关系图<附件五>)。
4.4.11本公司QMS的基本框架如下图所示:
相关文件:
(1)《相关方管理及沟通程序》 ******-CX-03
5 领导作用
限责任公司实施日期2018年01月01日附件五:质量管理体系过程关系图
附件六:文件清单
限责任公司实施日期2018年01月01日附件六:质量管理体系品质流程图。
ISO9001:2015版质量手册(完整)
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本质量手册描述了本公司的质量方针、质量目标并对本公司质量管理体系提出了具 体要求, 从而确保本公司的产品及服务能满足顾客和相关各方的需求, 并通过持续改进, 使本公司的产品和服务能适应并满足顾客当前的和未来的需求的变化。
本质量手册是我公司质量管理的法规,也是我公司向顾客做出质量保证和满足顾客 以及相关各方合理期望的承诺。是我公司开展内部质量审核和管理评审等质量活动的依 据,是我公司质量管理总的纲领性文件。
四川******科技有限责任公司
质量管理体系手册
(依据 GB/T19001-2016 IDT ISO9001-2015 标准修订)
文件编号: ******-QMS-2018 文件版本: A0 制定日期: 2017 年 12 月 31 日 生效日期: 2018 年 01 月 01 日
制定: 审核: 批准:
现批准下发执行,本公司全体员工必须认真学习、理解质量方针,并将质量手册所 规定的各项程序要求贯彻落实到日常工作中,以实现我公司质量目标及经济效益。
本质量手册含封面共 44 页 自 2018 年 01 月 01 起生效
四川 ****** 科技有限责任公司
总经理: 日 期:
第 5 页 共 43 页
四川******科技有 限责任公司
四川******科技有 限责任公司
文 名 称
文件编号 版 本 号
质量手册
QMS-01 A0
第 3 页 共 43 页
四川******科技有 限责任公司
0.1 企业简介
文 件 名 称
文件编号 版 本 号 实施日期
质量手册
QMS-01 A0
2018 年 01 月 01 日
四川******科技有限责任公司(以下简称“公司” )于 2004 年成立于中国科 技城-四川绵阳,注册资本为 2000 万元,是国家认定的高新技术企业。 表 2-1 公司股东构成表 序号 1 2 3 4 股东名称 四川************有限公司 香港********有限公司 天津市**********有限公司 自然人 合计 出资额 838.84 600 418.56 142.6 2000 股权比例(%) 41.942 30 20.928 7.13 100
ISO90012015质量手册-英文版
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Quality Management SystemPolicy ManualISO 9001:201511-8-17Date Printed: __________Quality Man ageme nt System PolicyMa nualRevisio n: 11-8-17 1.Quality Man ageme nt System ScopeCOMP ANY NAMESig nature: Date:COMPANY NAME establishes this quality policy man ual to impleme nt and mai ntain a quality man ageme nt system meeti ng the requireme nts of ISO 9001:2015, to en sure customer satisfaction in the manu facturi ng ofstamped, formed, machi ned and fabricated metal parts, weldme nts, subassemblies and pai nting of metal parts to customer and COMPANY NAME specificati ons1.1.Non-applicable Clauses of ISO 9001:1.1.1.8.3 Product Desig n & Developme nt of Products & Services —COMPANY NAME is acustomman ufacturer and desig ns are provided by our customers.2.Quality Policy Stateme ntCOMPANY NAME is committed to continually improving all products and services to achieve our customer ' s expectati ons.We do this by:1)Liv ing our values,2)Providi ng opport un ities for employee in volveme nt, motivati on and trai ning,3)Develop ing, docume nti ng and follow ing processes.3.Quality ObjectivesCOMPANY NAME s quality management system objectives are to enableCOMPANY NAMEto be our customers choice by:1)Achievi ng satisfactory rati ngs on quality, delivery and other key metrics tracked and reported by our customersthrough their formal supplier evaluati on and performa nee systems,2)Achieving a level of 700 ppm as tracked through COMPANY NAME s RA system for customers without a3)fAcmial/sreuip|ailier5%aouatiiioiie sdetemr^ it(q tiaiity, OMPANY NAME warehouse for customers without a formalsupplier evaluation system for delivery.Man ageme nt ApprovalName: Title:Paul Gintner Preside ntCOMP Quality Management System Policy ANY Manual NAME Revision: 11-8-174.Context of the Organization4.1.Understanding the Organization & Its ContextTop Management determines the external and internal issues that are relevant to our quality management system and its strategic direction, and that affect our ability to achieve the intended results.COMPANY NAME is a contract manufacturer in a competitive market, therefore we must maintain on-time delivery, product quality, and good customer service. Our key internal issues are to maintain production capacities, including competent people, capable processes, and maintained equipment.COMPANY NAME monitors and reviews information relevant to internal and external issues through ourmanagement review meetings.4.2.Understanding the Needs and Expectations of Interested PartiesDue to their potential effect on the organization 's ability to consistently provide products thatmeet customer requirements, Top Management determines:a)The interested parties that are relevant to the quality management system;b)The requirements of these interested parties that are relevant to the quality management system.COMPANY NAME ' s Top Management has determined that our customers, suppliers, employees, owners (Ottertail) and regulators (OSHA) are the interested parties that we need to be concerned with and will strive to meet their needs and expectations.Top Management monitors and reviews relevant measurements and information about these interested parties and their relevant requirements through management review meetings.4.3.Determining the Scope of the Quality Management SystemTop Management determines the boundaries and applicability of the quality management system to establish its scope. (Ref. Section1.)When determining this scope, Top Management has considered:a)The external and internal issues referred to in 4.1.b)The requirements of relevant interested parties.c)The products and services of the organization.We apply all the requirements of the standard that are applicable within the scope of the quality management system. With only one exclusion section 8.3 Product Design & Development of Products & Services - (Ref. Section 1.1.1)Top Management ensures the scope of the quality management system is available and maintained, as documented in Section 1, including the types of products and services covered by the quality management system, and justification for any requirements determined not applicable to the scope of the quality management system.Top Management ensures conformity to the standard(s) referred to in Section 1, and that any requirements determined as not applicable do not affect our ability or responsibility to ensure the conformity of our products and services and the enhancement of customer satisfaction.COMP ANY NAME Quality Management System PolicyManual Revision:11-8-174.4.Quality Management System and Its Processes4.4.1.Top Management establishes, implements, maintains, and continually improves aquality management system, including the processes needed and their interaction, in accordance with the requirementsof the standard.Top Management determines the processes needed for the quality management system and their application throughout theorganization, and:a)Determines the inputs required and the outputs expected from these processes;b)Determines the sequence and interaction of these processes (Ref. Figure 1);c)Determines and applies the criteria and methods (including monitoring, measurements, and related performanceindicators) needed to ensure the effective operation and control of these processes;d)Determines the resources needed for these processes and ensures their availability;e)Assigns the responsibilities and authorities for these processes;f)Addresses the risks and opportunities as determined in accordance with Section 6.1;g)Evaluates these processes and implements any changes needed to ensure that these processes achieve their intendedresults;h)Improves the processes and the quality management system.Customer UsesProduct ..COMP ANY NAMEQuality Man ageme nt System Policy Ma nualRevisio n: 11-8-17Figure 1 -Quality Man ageme nt System ProcessesCOMPA NY NAME QMS Process FlowCustomer Feedback Captured and Utilized for Con ti nu ousImproveme nt and FutureQuotesQuote Providedto Customer*See Figure 2 to refere nee specific processesthat facilitate the COMPANY NAME QMSProcess FlowInputsRiskCustomer Requireme ntsOrder Qty, Due date and ContainerInputsOutputsInputsCustomerPlaces Order* Job CreatedOutputsMaterial Delivery DateInputsOutputs -InputsJob scheduled, Material Delivery, WC Load,Contain ersOutputs Job PlannedProcess JoLabeled Product and In specti on DataInputskProduct Placed in -Inventory(EDI/Forecast In accuracy andorder can celati onRiskMon itori ngZ\Daily forecast and ordercon firmati onMonitoringRiskMaterial availability, SupplierOTDMon itori ngComm uni cati on with Sales4 Team, Supplier Performa nee/Report CardsRiskfWC Capacity, BOM Item Availability, Man PowerVJMon itori ngDaily Excepti on Report ing,Comm un icati on with Producti on and Daily Pla nn ers,.■ .Weekly Load Report Meeti ngRjskf :Mach ine, Man power, Tooli ng, Safety, Process Adhere nee, ■ 卜OSS OTD, Part Quality 】Mon itori ngProductivity, MDI data, LPA program, Safety Audit, Delivery to the Warehouse, ■. EQCP ^Supplier Report CardsRjskMonitoringDelivery to the Warehouse, Preservati on of product, Inven tory AccuracyMDI Data, Ran dom Inven tory Audits,FIFO processes, \.OutputCOMPANYNAMECore Flow Processes Support Processes Man ageme nt ProcessesSLS2-002 Process Customer OrdersSee STD2-004 and STD2-005 forInputs/Outsputs/KPI's for all Supportand Management processesQuality Man ageme nt System Policy ManualRevisio n: 11-8-17 Figure 2 -Quality Man ageme nt System Refere nee ProcessesRev:11-08-17■ Product Shipped to the Customer SHP2-001〔Ship Customer Orders4.4.2.Top Management ensures the organization:a)Maintains documented information to support the operation of its processes;b)Retains documented information to have confidence that the processes are being carried outas planned.This documentation includes the “Quality Manual ”, which consists of this Quality SystemPolicy Manual, as well as the quality system procedures, which are located and controlled asdefined under documentation requirements per Section 7.5.5.Leadership5.1.Leadership & Commitment5.1.1.GeneralTop Management demonstrates leadership and commitment with respect to the quality managementsystem by:a)Taking accountability for the effectiveness of the quality management system;b)Ensuring the quality policy statement and objectives are established for the qualitymanagement system and are compatible with the context and strategic direction of theorganization;c)Ensuring the integration of the quality management system requirements into the organization's business rpocesses;d)Promoting the use of the process approach and risk-based thinking;e)Ensuring that the resources needed for the quality management system are available;f)Communicating the importance of effective quality management and of conforming to the qualitymanagement system requirements;g)Ensuring that the quality management system achieves its intended results;h)Engaging, directing, and supporting personnel to contribute to the effectiveness of thequality management system;i)Promoting improvement;j)Supporting other relevant management roles to demonstrate their leadership as it applies to their areas of responsibility.5.1.2.Customer FocusTop Management demonstrates leadership and commitment with respect to customer focus by ensuringthat:a)Customer and applicable statutory and regulatory requirements are determined, understood,and consistently met;b)The risks and opportunities that can affect conformity of products and services and theability to enhance customer satisfaction are determined and addressed;c)The focus on enhancing customer satisfaction is maintained.5.2.Policy5.2.1.Establishing the Quality PolicyTop Management establishes, implements, and maintains a quality policy statement that:a)Is appropriate to the purpose and context of the organization and supports its strategicdirection;b)Provides a framework for setting quality objectives;c)Includes a commitment to satisfy applicable requirements;a) b) c) 5.3. Top Managementb) c) d) e) Ensuring that the quality management system conforms to the requirements of the standard, per Section 1; Ensuring that the processes are delivering their intended outputs;Reporting on the performance of the quality management system and on opportunities forimprovement , in particular to top management;Ensuring the promotion of customer focus throughout the organization;Ensuring that the integrity of the quality management system is maintained when changes tothe quality management system are planned and implemented. Give assurance that the quality management system can achieve its intendedresult(s);Enhance desirable effects; Prevent, or reduce, undesired effects; Achieve improvement. d) Includes a commitment to continual improvement of the quality management system.5.2.2. Communicating the Quality PolicyTop Management ensures the quality policy statement is:Available and maintained as documented information, ref. Section 2; Communicated, understood, and applied within the organization; Available to relevant interested parties, as appropriate.Organizational Roles, Responsibilities, & AuthoritiesTop Management ensures that the responsibilities and authorities for relevant roles are assigned, communicated, and understood within the organization.6. Planning6.1. Actions to Address Risks & Opportunities6.1.1. When pla nni ng for thequality management system, Top Management considers the issues referred to in 4.1 and the requirements referred to in 4.2, and determines the risks and opportunities that need to be addressed to: a) b)c) d)6.1.2. Top Management plans:a) Actions to address these risks and opportunities; b) How to:1) Integrate and implement the actions into its quality management systemprocesses;2) Evaluate the effectiveness of these actions.Top Management ensures actions taken to address risks and opportunities shall be proportionate to the potential impact on the conformity of products and services. Top Management has addressed risks and opportunities through the implementation of the quality management system, specifically through the procedures and processes we ' ve defined with the intention to prevent risks and address opportunities.6.2.Quality Objectives & Planning to Achieve ThemCOMP ANY NAMEQuality Management System PolicyManual Revision: 11-8-176.2.1.Top Management establishes quality objectives at relevant functions, levels, and processesneeded for the quality management system.Top Management ensures the quality objectives:a) Are consistent with the quality policy statement;b)Are measureable;c)Take into account applicable requirements;d)Are relevant to conformity of products and services and to enhancement of customersatisfaction;e)Are monitored;f)Are communicated;g)Are updated as appropriate.Top Management maintains documented information on the quality objectives.6.2.2.When planning how to achieve its quality objectives, Top Management determines:a) What will be done;b) What resources will be required;c) Who will be responsible;d)When it will be completed;e)How the results will be evaluated.Top Management plans to achieve objectives by defining our quality management systemprocedures and processes. Top Management evaluates results and improvement actions throughthe management review process, including document and tracking actions.6.3. Planning of ChangesWhen the need for changes to the quality management system are determined, Top Management ensuresthe changes are carried out in a planned manner, considering: a) The purpose of the changes and theirpotential consequences;b) The integrity of the quality management system;c)The availability of resources;d)The allocation or reallocation of responsibilities and authorities.7.Support7.1.Resources7.1.1.GeneralTop Management determines and provides the resources needed for the establishment,implementation, maintenance, and continual improvement of the quality management system,considering:a) The capabilities of, and constraints on, existing internal resources;b) What needs to be obtained from external providers.7.1.2.PeopleTop Management determines and provides the personnel resources necessary for the effectiveimplementation of its quality management system and for the operation and control of itsprocesses.7.1.3.InfrastructureCOMP ANYNAMEQuality Management System PolicyManual Revision: 11-8-17 Printed copies are uncontrolled.COMPANY NAME Quality System Policy Manual -2015 (1)Page 11 of 19Top Management determines, provides, and maintains the infrastructure necessary for the operation of its processes and to achieve conformity of products and services.7.1.4. Environment for the Operation of ProcessesTop Management determines, provides, and maintains the environment necessary for the operation of its process and to achieve conformity of products and services.7.1.5. Monitoring & Measuring Resources7.1.5.1. GeneralTop Management determines and provides resources needed to ensure valid and reliable resultswhen monitoring or measuring is used to verify the conformity of products and services torequirements, ensuring the resources provided:a) Are suitable for the specific type of monitoring and measurement activities beingundertaken;b) Are maintained to ensure their continuing fitness for their purpose.Top Management ensures appropriate documented information is retained as evidence of fitnessfor purpose of the monitoring and measurement resources.7.1.5.2. Measurement TraceabilityWhen measurement traceability is a requirement, or is considered to be an essential part of providing confidence in the validity of measurement results, the Quality Department ensures measuring equipment is:a) Calibrated or verified, or both, at specified intervals, or prior to use, against measurementstandards traceable to international or national measurement standards; when no such standards exist, the basis used for calibration or verification are retained as documented information; b) Identified in order to determine their status;c) Safeguarded from adjustments, damage, or deterioration that would invalidate the calibrationstatus and subsequent measurement results.Assigned personnel determine if the validity of previous measurement results have been adversely affected when measuring equipment is found to be unfit for its intended purpose, and take appropriate action as necessary.7.1.6. Organizational KnowledgeTop Management determines the knowledge necessary for the operation of its processes and to achieve conformity of products and services.Top Management ensures this knowledge is maintained and made available to the extent necessary.When addressing changing needs and trends, Top Management ensures current knowledge is considered and determines how to acquire or access any necessary additional knowledge and required updates.Top Management has addressed this requirement through the documented processes and procedures of the quality management system, as well as through the retained information supporting the quality management system processes.。
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ISO 9001:2015Quality ManualA quality manual is a document that states the company’s intentions for operating the processes within the quality management system. It can include policies for all areas of the business that affect your ability to make high-quality products and meet your customers’ and ISO’s requirements. These policies define how your department managers will implement procedures within the boundaries specified in the quality manual. The use of Quality Manual are as follows:1.To communicate management’s expectations to employees2.To demonstrate the company’s plan to conform to therequirements of ISO 9001:20153.To demonstrate the fulfilment of Clause 5.3, thatorganizational roles, responsibilities and authorities are assigned, communicated and understood4.To provide a starting point for auditors:1.Internal2.Customer3.ISO Certification BodyTo develop a quality manual, you might consider these steps: 1.List policies to be written (note any ISO requirements thatdo not apply).2.Draft policies based on applicable ISO requirements.3.List operating procedures or refer to them as appropriate.4.Determine the format and structure of the manual andmake the first draft.5.Circulate the draft manual for input from all departmentsand address inadequacies identified.6.Attain a formal approval and release.The contents of your quality manual are completely up to you. But, remember that everything you say you do, you must show evidence that you really do it! So be careful what you include and make sure the policies reflect actual practices. Here are some common topics included in quality manuals.the scope of QMSQuality policyExplanation of the company’s documentation structureOrganizational chartPolicy statements for each applicable ISO requirementReference to operating procedures1) The scope of the Quality Management System. This is in place to identify the limit of the system and is based on the scope agreed with the registrar to be placed on the ISO9001 certificate. This is the explanation of what your company does, be it “Design and Manufacture of the bevel Gear,” “Machining Services for Customers in the oil and service Industry,” or “Providing Fast Food for People in Kuwait city.” The second part of the scope requirement is to identify any exclusions from the standard. In many cases, the Quality Manual will identify none, but the most common exclusion is the requirement of the ISO 9001 standard for “Design & Development” for companies such as a machining shop, which works exclusively from customer drawings and does not design any products itself.2) The documented procedures established for the Quality Management System (or references): ‘Documentation’ means anything written down or captured in some form such as written procedures, policies, checklists, forms, or graphics, drawings, flowcharts, diagrams, IT systems. This is called ‘documentedinformation’ in the current version (2015) of ISO 9001. Confusingly, they have also decided to use the same term for what was formerly called ‘records’ – those things that showed what had been done, such as registers, logs, competed for forms, reports, meeting minutes and so on. ‘Documented information’ in 9001 terms means both the ‘written stuff’ that describe your quality system and say how it should operate (eg, flowcharts, procedures, policies, checklists) and the ‘written stuff’ that shows what was done. A system must be documented to achieve ISO 9001 certification because having certain documented information is required by the Standard. All the documents t needs to control how things are done, whether procedures, flowcharts, checklists, forms, IT systems or any other media or format that work in your business. But note that no mandatory procedures are prescribed. Nor a quality manual. What can confuse people is that actually, you can choose what your documents look like, what format and structure you use, and what to put in them. Provided you meet these requirements. You can use one or many formats, from checklists and flowcharts to intranets, wikis or workflow embedded into IT systems. You can use any media, hardcopy or soft, including intranet, online, internet or wiki. One often used way to do that was with a thingcalled a ‘quality manual’. And you can still do that if you choose. And it can be in hard copy (paper) or softcopy: online documents like web pages, help files or IT systems. And you can write your document in various ways, from easy and user-friendly to bureaucratic, verbose and very hard to follow. And such a manual may be the only document you have for your system, or it may be one of a number of documents. Or something in between.3) A description of the interaction of processes. This is most simply done with a flowchart that identifies all the processes in the organization with arrows showing how they connect. While an in-depth flowchart may help you to better understand the interactions between processes in your organization, a simple top-level flowchart is all that is needed for most people to understand the basics. Example of Quality Manual1.0 Company ProfileInclude your company profile1.1 The mission of the FirmOur mission is to enhance mobility through innovation, leadership and public service. Innovation by providing unparalleled value combined with flexibility and risk-taking ability, leadership by delivering exceptional performance in every domain and corporate responsibility through service to society.1.2 The vision of the FirmTo strive relentlessly with an aim to achieve excellence in all businesses that we venture into, with the objective of becoming an organization that all its employees and associates are proud of.2.0 Organization ScopeDesign, Development of Land, Construction Sales of Residential and Commercial Complexes2.1 Exclusions:NIL2.1 Quality PolicyXXX is committed to delivering quality construction work with promised amenities, in time possession, which meets and exceeds the needs & expectation of our customers. We promise our valued customer’s commitment to excellence in each activity by each employee in the organization by adopting innovative and best in class engineering and management practices with continual improvement in business and quality management system as a part of our efforts for enhancement in customer satisfaction while assuring 100% quality and quantity.2.2 Key ObjectivesTimely completion of projectsIncrease Customer satisfactionReduce Customer Complaint3.0 Glossary & Abbreviations4.0 Context of Organization4.1 Understanding the organization and its context: Shah Promoters and Developers determine external and internal issues that are relevant to its purpose and its strategic direction and that affect its ability to achieve the intended result(s) of its quality management system through PEST and SWOT. The external and internal issues identified throughPEST and SWOT are continuously being monitored and reviewed by CEO.PESTSWOT4.2- Understanding the needs and expectations of interested partiesxxx has determined the interested parties who are relevant to the xxx Quality management system and the requirement of the interested parties in order to prevent the potential effect on the organization’s ability to consistently provide products and services which meet the customer and applicable statutory and regulatory requirements.4.3 Determining the scope of the quality management systemThe organization had determined the scope of the Quality management system by considering external and internal issues, the requirement of relevant interested parties and Product & Service of the organization.The scope of Quality Management System isDesign, Development of Land, Construction Sales of Residential and Commercial ComplexesExclusions:NIL4.4 Quality management system and its processes4.4.1: xxx has determined the processes needed for the quality management system and their application throughout the organization in Process map & Interactions of processes.xxx has determined the inputs required and the outputs expected from each process in individual process map addressed in the documented information of each process.xxx has determined the sequence and interaction of the processes in Process map & Interactions of processes.xxx has determined and applied the criteria and methods (including monitoring, measurements and related performance indicators) needed to ensure the effective operation and control of these processes in the documented information of each process.xxx has determined the resources needed for these processes and ensure their availability in the documented information of Support process.xxx has assigned the responsibilities and authorities for each processxxx has addressed the risks and opportunitiesxxx has been evaluating these processes and implementing any changes needed to ensure that these processes achieve their intended results and improve the processes and the quality management systemImprove the processes and the quality management system4.4.2- xxx is also maintaining documented information to support the operation of its processes and retaining documented information to have confidence that the processes are being carried out as planned.5.0 Leadership5.1 Leadership and commitmentXxx Management has demonstrated leadership and commitment with respect to the quality management system through1.Taking accountability for the effectiveness of the qualitymanagement system by periodical review of qualitymanagement system through management review meeting, Quality objectives review and providing necessary resources.2.Management has established the quality policy andquality objectives for the quality management system and is compatible with the context and strategic direction of the organization.3.Management has determined the organizationalprocesses and integrated with the quality management system requirement through process map & Interaction this can be demonstrated.4.The established procedure for promoting the use of theprocess approach and risk-based thinking.5.Ensuring that the resources needed for the qualitymanagement system are available, this is being periodically reviewed through management review meeting.municating the importance of effective qualitymanagement and of conforming to the quality management system requirements7.Ensuring that the quality management system achievesits intended results8.Engaging, directing and supporting persons to contributeto the effectiveness of the quality management system by providing training, conducting awareness programs and 9.Promoting improvement by introducing the suggestionscheme, Kaizens and conducting meetings.10.Supporting other relevant management roles todemonstrate their leadership as it applies to their areas of responsibility.5.1.2 Customer focusXxx management has demonstrated leadership and commitment with respect to customer focus by ensuring that: 1.Customer and applicable statutory and regulatoryrequirements are determined, understood and consistently met.2.The risks and opportunities that can affect conformity ofproducts and services and the ability to enhance customer satisfaction are determined and addressedc) The focus on enhancing customer satisfaction is maintained and procedure for customer satisfaction is addressed5.2 QUALITY POLICYXXX is committed to delivering quality construction work with promised amenities, in time possession, which meets and exceeds the needs & expectation of our customers. We promise our valued customer’s commitment to excellence in each activity by each employee in the organization by adopting innovative and best in class engineering and management practices with continual improvement in business and quality management system as a part of our efforts for enhancement in customer satisfaction while assuring 100% quality and quantity. We are also committed to serving society as a whole by generating through clean development mechanism (CDM) project.5.2.1 Establishing the quality policyXxx management has established, implemented and maintained a quality policy that:1.is appropriate to the purpose and context of theorganization and supports its strategic direction.2.Provides a framework for setting quality objectives3.Includes a commitment to satisfy applicable requirements4.Includes a commitment to continual improvement of thequality management system5.2.2 Communicating the quality policyThe quality policy is1. Available and be maintained as documented informationmunicated, understood and applied within theorganization through display, Training and periodical review.3.Available to relevant interested parties, as appropriate. 5.3 Organizational roles, responsibilities and authoritiesXxx management has ensured that the responsibilities and authorities for relevant roles are assigned communicated and understood within the organization. While assigning roles, responsibility and authority, top management has considered and ensured that1.The quality management system conforms to therequirements of this International Standard2.The processes are delivering their intended outputs3.Reporting on the performance of the quality managementsystem and on opportunities for improvement, in particular, to top management4.The promotion of customer focus throughout theorganization5.The integrity of the quality management system ismaintained when changes to the quality management system are planned and implemented.Roles, responsibility and authorities assigned are available in process & as per Organization chart wiseDirectorsResponsibilityOverall Responsibility for formulating and communicating Quality Policy & Quality objectives.Formulation of Strategy for continuous up gradation of Business and Quality System.Ensure periodic assessment of the performance of Quality System.Approval of Quality System Manual.Budget Approval for the organization.Overall Responsibility for Business Development & all financial issues.Provision of resources as required.Strategic decisions on developments and technical setups. To provide the leadership for efficient implementations of the system.Authorities:Approval of customers orders, P.O. and Cheque.Sanctioning leaves of all Staff.Approval of funds for Training needs.All the authorities of downline personnel.Chairing Management review meetings.Project PlanningResponsibilities:Overall coordination between client, project managers and office department.Follow up for Schedules.The entire responsibility of Quality.Monitoring Client Satisfaction.Coordination with the consultants.Disciplinary actions against the staff.Prime responsibility for the safety at the siteProvision of a suitable working environmentEnsure the quality system is established, implemented and maintained.Authorities:Appointment of the staff, engineers and tech staff.Sanctioning the Leaves to Staff.All the authorities of downline personnel.Project ManagersResponsibilities:Responsibilities for the entire Project work, i.e. Quality, Quantity and Time.Coordination with consultants and contractors.Coordination with Consultants for drawings.Coordination with the Site engineers.Coordination with the client for the ongoing changes in drawings and projects.Monitoring site engineers work on a daily basis.Reporting to the GM Projects on the above issuesResponsibilities for safety at the site. (Good working environment).Authorities:Make or force a required decision at all levels to achieve project objectives.Initiate actions on the Contractors and consultants for Quality, Quantity and Timeframe issues related to project work.To stop and initiate corrective actions on non–confirming products/services.Site SupervisorResponsibilities:Coordinating with all staff for the Quality related issues of Construction.Daily Labour Handling for Civil Work.Monitoring of Work progress and daily reporting.Preparation of work progress report / Quality Documentation.Control of non – conformities on siteSafety at site / Construction work.Coordination with the Site Contractor for the daily work requirements.Coordination with external agencies for calibration of instruments and material testing.Authorities:Initiate actions on the staff for non-fulfillments of the documentation related qualityTo stop and initiate corrective actions on non–conforming products.Site engineerResponsibilities:Monitoring of site and labour contractors.Monitoring of work progress and daily reportingPreparation of work progress report.Control of non – conformities on site.Ensuring instruments are properly used and are with the status of calibration.Track Project progress & produce regular weekly status reports.Coordinate with all labour contractors to achieve continuous progress at the site as per schedule.Follow up with the Project manager for pending decisions/drawings/building specifications.Communicate management decisions and information to Site subordinate staff.Ensuring the worker’s safety at site and usage of safety equipment.Implementation and follow up and regular monitoring of implemented ISO 9001 system at the site.Coordination with the Quality Person for Quality related issues.Coordinating Material Accountability at siteAuthorities:Initiating the corrective and preventive actions as needed on contractors and consultants.Decision making on during any emergencies at the site.In-charge Marketing:Managing & motivating the sales force towards the achievement of target.Preparation of Sales plan.Annual sales forecast.Monthly sales forecast.Implementation of sales plan.Authorities:Approval of documents as per the Master list of Quality System Document.Authorized to decide corrective & preventive action.Authorized to obtain concessional acceptance for non – conforming product from the customer.InCharge – ADMIN + ACCOUNTResponsibilities:Responsible for tendering activity.Customer order review.Handling and coordinating customersIdentification of resources, as applicable.Document & Data control system pertaining to his department.Maintain all documents related to the quality system.Coordinator for Management reviews.Promoting awareness of customer requirements throughout the Organization.Compliance & effectiveness of the training system.Suitable working environment (cleanliness, ventilation, lighting, safety etc.).Record maintaining for Sales Register, Rent Register, Sale Files, Stationery and Office equipment.Archiving and record keeping of old files.Payroll Monthly: Salary –To release monthly salary of the employees as per policy finalized.Leave – To keep the record of leave as per policy finalized.Annual Allowance – To release annual allowances as per policy finalized.Employee Record – To update employee details as per organization Policy and QMS.To prepare an appointment letter, confirmation letter, experience letter & all employee-related matter as per policy finalized with the help of the Managing Director.Authorities:Approval of customer orders.Approval of documents as per the master list of Quality System Document.Authorized to decide corrective & preventive action.In charge Purchase:Responsibilities:Overall in charge of purchase activities.Identification of resources, as applicable.Purchasing system – Evaluation, selection, purchasing, monitoring.Document & Data control system pertaining to his department.Corrective / Preventive action system (subcontractor non-conformances, in particular.)Control of recordsAuthorities:Authorized to review & approve purchasing documents.Authorized to select & discontinue sub-contractor6.0 Planning6.1 Actions to address risks and opportunities6.1.1Xxx is addressed the issues, requirements the risks and opportunities1.give assurance that the quality management system canachieve its intended result(s)2.Enhance desirable effects3.Prevent, or reduce undesired effects4.achieve improvement6.1.21.actions to address these risks and opportunities2.How to1.integrate and implement the actions into its qualitymanagement system processes2.Evaluate the effectiveness of these actions6.2.2 Quality objectives and planning to achieve them 6.2.1Xxx establish quality objectives at relevant functions, levels and processes needed for the quality management system.The quality objectives shall1.Be consistent with the quality policy2.Be measurable3.Take into account applicable requirements4.Be relevant to the conformity of products and services andto the enhancement of customer satisfaction5.Be monitored6.Be Communicated7.Be updated as appropriate6.2.2 Xxx achieve its quality objectives,1.What will be done?2.What resources will be required?3.Who will be responsible?4.When it will be completed5.How the results will be evaluatedOur Quality Objectives are as below:Timely completion of projectsEnergy Generation Per YearIncrease Customer satisfactionReduce Customer Complaint6.3 Planning of changesXxx determines the need for changes to the quality management system, the changes are carried out in a planned manner1.the purpose of the changes and their potentialconsequences2.the integrity of the quality management system3.the availability of resources4.the allocation or reallocation of responsibilities andauthoritiesXxx has determined the processes needed for the quality management system and their application throughout the organization in Process map & Interactions of processes7 Support7.1 Resources7.1.1 GeneralXxx is determined and provide the resources needed for the establishment, implementation, maintenance and continual improvement of the quality management system. Xxx is consider1.the capabilities of, and constraints on, existing internalresources2.what needs to be obtained from external providersHR determine and provide the resources needed to implement and maintain the quality management system and continually improve its effectiveness and to enhance customer satisfaction by meeting customer requirement. The resources will be in the form ofHuman resources including qualified personnel for verification activities.Manufacturing machines, Test Equipment’s &infrastructure.Provide raw material & other inputs for the realization of the product.Providing funds.The Required resources are identified in the event of new Process Development / Business plan review, Mfg Process Flow, also based on the Organization performance review in MRM and monthly business reviews.7.1.2 PeopleXxx determine and provide the persons necessary for the effective implementation of its quality management system and for the operation and control of its processes. HR along with respective process IN CHARGE ensures that personnel performing work affecting product quality is competent and training to give on the basic operation and control of its processes.7.1.3 InfrastructureXxx is determined, provide and maintain the infrastructure necessary for the operation of its processes and to achieve conformity of products and services. Infrastructure can include1.buildings and associated utilities2.equipment, including hardware and software3.transportation resourcesrmation and communication technologyAt Xxx management determine, provide and maintain the infrastructure needed to achieve conformity to product requirements & in identifying the required resources the PARTNER play a key role based on their day to day interactions with respective IN CHARGE’s and employees 7.1.4 Environment for the operation of processesXxx is determined, provide and maintain the environment necessary for the operation of its processes and to achieve conformity of products and services. A suitable environment can be a combination of human and physical factors1.Social (e.g. non-discriminatory, calm,non-confrontational)2.Psychological (e.g. stress-reducing, burnout prevention,emotionally protective)3.Physical (e.g. temperature, heat, humidity, light, airflow,hygiene, noise).Project in coordination with respective IN CHARGE determines and manages the work environment needed to achieve conformity to product requirement and reviewed ongoing basis.7.1.5 Monitoring and measuring resources7.1.5.1 GeneralXxx is determined and provide the resources needed to ensure valid and reliable results when monitoring or measuring is used to verify the conformity of products and services to requirements. The organization shall ensure that the resources provided1.are suitable for the specific type of monitoring andmeasurement activities being undertaken2.are maintained to ensure their continuing fitness for theirpurposeXxx is retained appropriate documented information as evidence of fitness for purpose of the monitoring and measurement resources7.1.5.2 Measurement traceabilityXxx is measurement traceability is maintained requirement if applicable for the instruments or is considered by them to be an essential part of providing confidence in the validity of measurement results,1.calibrated or verified, or both, at specified intervals, orprior to use, against measurement standards traceable to international or national measurement standards; when no such standards exist, the basis used for calibration or verification shall be retained as documented information2.identified in order to determine their status3.safeguarded from adjustments, damage or deteriorationthat would invalidate the calibration status and subsequent measurement resultsXxx is determined the validity of previous measurement results has been adversely affected when measuring equipment is found to be unfit for its intended purpose, and shall take appropriate action as necessary.Control of Monitoring & Measuring Equipments. Measurement & Monitoring system is well equipped and the system has complete control over the monitoring andMeasuring Equipment. The measurement methods used are evaluated to ensure that they are appropriate and reliable. To ensure that the measuring equipment operates effectively and give reliable results, we have taken the following steps:Equipments are maintained properly and are calibrated & adjusted as and when needed. Necessary safeguards are in place to take care of adjustments that could lead to invalid results.Calibrations are carried out as per national standards (by NABL accredited laboratories only). Where no such standard exists, the basis used for calibration or verification is recorded. The calibration records include the last date of calibration, calibrating agency (for the external agency), calibration result, and frequency of calibration as per the process and/or instrument requirement and the next calibration date. The required accuracy is identified and compared to the measurement that meets expectations. Identification of appropriate equipment is accomplished by tagging, labelling, numbering or by including it in a calibration/maintenance database.。