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시스템 · 문서 62개

ISO 9001 Quality Management System

시스템 · SYS-50263

ISO 9001 Quality Management System 템플릿 미리보기
  • 문서 62개
  • 라이브러리 폴더 하나에 모두 담겨 제공

A quality management system built on ISO 9001 for organisations of any size, with the documents to set it up, run it and audit it.

The system has seven plans, one policy, one procedure and 53 forms, registers and checklists. Together they cover quality risk assessment, procurement, supplier questionnaires and scorecards, verification of quality requirements, operational control, inspection and test plans, and internal audits.

The documents refer to each other, and arrive together in one folder of your Library with every reference pointing at your own copies.

Written by SafetyDocs safety experts, who have been writing safety documents since 2004.

Quality Management System 관리 계획서 미리 보기

Quality Management System

관리 계획서Version 3

Introduction

Company is committed to developing and maintaining a Quality Management System (QMS) that demonstrates our commitment to customer satisfaction. This commitment is placed within an environment that has safety as a priority, is focused on the service it provides, and fosters continual improvement.

The purpose of this manual is to describe the scope of the quality system, define the accountabilities of all people involved, and provide procedures for testing and quality inspection for all activities. The manual is used to direct internal activities and inform external parties who require information about our quality systems.

This QMS Manual documents how we implement maintain and continually improve our QMS. It identifies the criteria and methods used to ensure the effective operation, and control of the system, and identifies the monitoring, analysis, information, and actions necessary to achieve business outcomes.

Senior management of the company determines the management of the external and internal issues that have an impact on the products and services that we deliver to our customers.

To understand the external issues, we will monitor and consider issues coming from:

  • legal and legislative requirements;

  • technology changes;

  • customer needs;

  • market competition;

섹션 11개 더

  1. Quality management framework
  2. Leadership
  3. Planning
  4. Support
  5. Operation
  6. 외 6개

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포함 내용

  1. Quality Management System

    관리 계획서 · 섹션 12개

    A Quality Management System manual built on AS/NZS ISO 9001:2016: policies, procedures, audits, management review and improvement.

    단독으로도 판매
  2. Verification of Quality Requirements Checklist

    양식 · 입력 항목 12개

    A checklist for verifying delivered goods or services against quality requirements: details, a pass or fail table, an overall result and approvals.

    단독으로도 판매
  3. Supplier Questionnaire-Quality

    양식 · 입력 항목 11개

    A supplier quality questionnaire covering certification, performance data, policies, subcontractors and a signed declaration.

    단독으로도 판매
  4. Quality Procurement Implementation Guide

    정책 · 섹션 5개

    A guide to implementing the Quality Procurement Procedure: its roles, step-by-step process and how to tailor it to each procurement.

    단독으로도 판매
  5. Quality Procurement Request Form

    양식 · 입력 항목 15개

    An internal form to request the purchase of goods or services, assess the quality impact and supplier, and sign off the recommendation.

    단독으로도 판매
  6. Supplier Evaluation Scorecard (Quality)

    양식 · 입력 항목 9개

    Scorecard for rating a supplier's quality capability across four sections, with notes and an approve, approve with conditions or not approved result.

    단독으로도 판매
  7. Quality Risk Assessment Form

    양식 · 입력 항목 15개

    A form to assess the quality risks of items and services you buy, with a four-step risk matrix and a register with worked examples.

    단독으로도 판매
  8. Interested Parties Register

    양식 · 입력 항목 5개

    A register of interested parties: who they are, what they need and expect, your objectives for each and their priority.

    단독으로도 판매
  9. Template

    SOP · 섹션 10개

    Blank standard operating procedure template with sections for purpose, scope, responsibilities, equipment, PPE, hazards, steps and change history.

    단독으로도 판매
  10. Operational Control Register

    양식 · 입력 항목 7개

    A register of the documented operational controls for your processes: whether each is in place, its procedure, version and responsible person.

    단독으로도 판매
  11. Infrastructure Responsibilities Register

    양식 · 입력 항목 2개

    Register that lists the departments and people responsible for infrastructure use and maintenance, and the infrastructure each looks after.

    단독으로도 판매
  12. Objectives Summary Form

    양식 · 입력 항목 7개

    A form for management to record an objective, its background, target and the resources required, with the responsible person's sign-off.

    단독으로도 판매
  13. Emergency Response Register

    양식 · 입력 항목 6개

    A register of a site's emergency response procedures: whether each is in place, its document, version and responsible person.

    단독으로도 판매
  14. Worker Training Record

    양식 · 입력 항목 10개

    A record of one worker's training in one course: who approved it, start and completion dates, description, expected outcomes and training type.

    단독으로도 판매
  15. Outsourced Process Register

    양식 · 입력 항목 9개

    A register for assessing outsourced processes: customer requirements, your requirements, validation and verification for each outsource company.

    단독으로도 판매
  16. Training Needs Register

    양식 · 입력 항목 8개

    Training needs register recording each role's responsibilities, required qualifications and competencies, training needs, dates and course details.

    단독으로도 판매
  17. Quality Project Management Plan

    관리 계획서 · 섹션 16개

    A Quality Project Management Plan covering scope, responsibilities, audits, non-conformances, inspection and testing, and change management, with forms and registers.

    단독으로도 판매
  18. Quarterly Objective and Targets Report

    양식 · 입력 항목 7개

    A quarterly register for reporting results against your key objectives and targets at the end of March, June, September and December.

    단독으로도 판매
  19. Annual Audit Schedule

    양식 · 입력 항목 1개

    A month-by-month schedule for planning safety, environmental or quality audits across the year, with a legend for planned and postponed audits.

    단독으로도 판매
  20. Internal Audit Plan

    관리 계획서 · 섹션 5개

    An Internal Audit Plan to set the audit's subject, scope, objectives, team and criteria, so audits are conducted efficiently and effectively.

    단독으로도 판매
  21. Roles and Responsibilities Schedule

    양식 · 입력 항목 1개

    A schedule for one role: its title, responsibilities, who it reports to, its escalation path and the authority it holds.

    단독으로도 판매
  22. Operations-Processes – Identification Form

    양식 · 입력 항목 3개

    A register for listing the operations and processes an organisation carries out, with an identifier and the location of each.

    단독으로도 판매
  23. Management Review Meeting Report

    양식 · 입력 항목 7개

    A form to record a management review meeting: attendance, discussion, previous action items and new actions.

    단독으로도 판매
  24. Corrective-Preventative Actions Register

    양식 · 입력 항목 7개

    Register to record the corrective and preventative actions to be taken from raised issues, with due dates, status and completion.

    단독으로도 판매
  25. Roles, Responsibilities, Accountabilities and Authorities Register

    양식 · 입력 항목 6개

    A register of position holders: role type, name, who they report to, delegated authority and tenure dates, for defining responsibility and accountability.

    단독으로도 판매
  26. Monitoring and Measuring Equipment Register

    양식 · 입력 항목 5개

    A register of monitoring and measuring equipment: identifier, name, procedure, and the dates of the last and next calibration or service.

    단독으로도 판매
  27. AS/NZS ISO 9001:2016 Internal Audit Checklist

    양식 · 입력 항목 41개

    A checklist for self-assessing your quality management system against AS/NZS ISO 9001:2016, with audit guidance, scope, auditors and space for findings.

    단독으로도 판매
  28. Incident Register

    양식 · 입력 항목 10개

    A register to record workplace incidents and near misses: when and where, what happened, who was involved, severity, status and the corrective actions taken.

    단독으로도 판매
  29. Compliance Evaluation Report

    양식 · 입력 항목 11개

    A compliance evaluation report for checking legislation, codes of practice and standards across health and safety, environmental and quality.

    단독으로도 판매
  30. Internal Audit Report

    양식 · 입력 항목 11개

    Helps auditors give management clear, objective and impartial information about what is going well and what needs to be improved.

    단독으로도 판매
  31. Compliance Requirements Register

    양식 · 입력 항목 3개

    A register of the regulatory and internal compliance requirements that apply to each process or function, with the legislation and a description.

    단독으로도 판매
  32. Risk Register

    양식 · 입력 항목 8개

    A form to record identified hazards and risk levels in the workplace, with current controls and recommended actions for uncontrolled risks.

    단독으로도 판매
  33. Quality Design Plan

    관리 계획서 · 섹션 12개

    A Quality Design Plan to manage the design process and control design output: roles, milestones, communication, verification and approval.

    단독으로도 판매
  34. Communications Program Schedule

    양식 · 입력 항목 5개

    Register of the communication protocols and timings with internal and external stakeholders, for workers, customers, regulators and contractors.

    단독으로도 판매
  35. Document Register

    양식 · 입력 항목 14개

    A register of the documents your organisation holds: numbers, versions, titles, purpose, author, key dates and approvals, for version control.

    단독으로도 판매
  36. Non-Conformance Report

    양식 · 입력 항목 12개

    A report to document and address deviations from project specifications or quality standards, with corrective, preventative and monitoring actions.

    단독으로도 판매
  37. Disaster Recovery Plan

    관리 계획서 · 섹션 9개

    A Disaster Recovery Plan to prepare for disasters and accidents, with policy, procedure, responsibilities, a plan template and supporting forms.

    단독으로도 판매
  38. Change Request Form

    양식 · 입력 항목 16개

    A form to detail and record a request for a change to systems or processes, with the change manager's initial risk analysis.

    단독으로도 판매
  39. External Quality Control Register

    양식 · 입력 항목 7개

    A register of critical control points for external supply: hazard, risk, monitoring, critical limits, corrective measures and records.

    단독으로도 판매
  40. Operational Control Development Worksheet

    양식 · 입력 항목 11개

    A worksheet for assessing documented controls: which procedures are in place, which need updating and which new documents are required.

    단독으로도 판매
  41. Objectives and Targets Register

    양식 · 입력 항목 5개

    A register of key objectives and targets, each with its performance metric and the person or area responsible.

    단독으로도 판매
  42. Emergency Response Plan

    관리 계획서 · 섹션 25개

    An Emergency Response Plan so workers know what to do in an emergency: evacuation, fire, first aid, spills, threats and bomb threats, with registers and checklists.

    단독으로도 판매
  43. Outsourced Process Schedule

    양식 · 입력 항목 3개

    A register of outsourced processes: the service provider for each and the quality control method used to check their work.

    단독으로도 판매
  44. Products Processes – Identification and Material Traceability

    양식 · 입력 항목 5개

    A register of products and processes with their identifier, name and location, for material identification and traceability.

    단독으로도 판매
  45. Internal Quality Control Register

    양식 · 입력 항목 8개

    A register of quality management roles and their responsibilities, required competencies, training needs, dates and course details.

    단독으로도 판매
  46. Worker Training and Induction Register

    양식 · 입력 항목 10개

    A register of the training and competencies each worker has completed, their licences and expiry dates, and whether they have been correctly inducted.

    단독으로도 판매
  47. Training Skills Responsibilities Register

    양식 · 입력 항목 8개

    A register of roles, responsibilities, required competencies and training needs, with training dates, course details and comments.

    단독으로도 판매
  48. Measuring and Calibration Register

    양식 · 입력 항목 5개

    A register of measuring and monitoring equipment with its procedure and the dates of last and next calibration or service.

    단독으로도 판매
  49. Inspection Test Plan

    관리 계획서 · 섹션 2개

    A blank inspection test plan to record activities, test methods, acceptance criteria, records and inspections, with approval and review sign-off.

    단독으로도 판매
  50. Work Groups Register

    양식 · 입력 항목 8개

    A register for keeping track of workplace work groups, their locations, members and health and safety representatives.

    단독으로도 판매
  51. Meeting Minutes

    양식 · 입력 항목 10개

    A meeting minutes form: attendees and signatures, the agenda, topics discussed, comments and the actions that follow.

    단독으로도 판매
  52. Product Approval Checklist

    양식 · 입력 항목 8개

    A checklist for approving a design for release: project details, component sign-off with Yes and No tick boxes, and an approval signature.

    단독으로도 판매
  53. Project Acceptance Criteria

    양식 · 입력 항목 7개

    A project acceptance criteria form: the criteria each deliverable must meet before acceptance, and a milestones table with planned dates.

    단독으로도 판매
  54. Test Protocols

    양식 · 입력 항목 4개

    A register of test protocols: each protocol's number and name, its date of issue and the date it is due for review.

    단독으로도 판매
  55. Monitoring and Measurement Schedule

    양식 · 입력 항목 3개

    A register of what is monitored and measured: the location, the responsible person or position, and the date or time of each check.

    단독으로도 판매
  56. Corrective and Preventative Actions Form

    양식 · 입력 항목 9개

    Record a corrective or preventative action: the issue and its seriousness, the evaluation, the action, who is responsible and the manager's sign-off.

    단독으로도 판매
  57. Quality Incident and Corrective Action Report Form

    양식 · 입력 항목 26개

    A quality incident and corrective action report: incident details, witnesses, investigation, root cause, preventative actions and sign-off.

    단독으로도 판매
  58. Monitoring Register

    양식 · 입력 항목 7개

    A register of the system items that need monitoring: responsibility, legislation, frequency, record retention period and comments.

    단독으로도 판매
  59. Organisation Chart

    양식 · 섹션 5개

    An organisation chart naming who holds each safety role, from the PCBU, owner or CEO through senior management and the health and safety team to workers.

    이 시스템에만 포함
  60. Disaster Recovery Response Register

    양식 · 입력 항목 8개

    A register of operations and activities, with whether an emergency recovery procedure is in place, its document, version and responsible person.

    단독으로도 판매
  61. Hazard Report Form

    양식 · 입력 항목 14개

    Hazard report form for workers to record a hazard, its exact location, when it was found and the recommended action, before it causes an incident.

    단독으로도 판매
  62. First Aid Worker Register

    양식 · 입력 항목 8개

    A register of your first aid officers: who manages the first aid kit, each officer's location and contact details, and their qualifications and expiry dates.

    단독으로도 판매

다루는 내용

시스템 구성 방식

규칙을 정하는 계획서부터 작업 당일 작업자가 하는 일까지, 각 문서는 자신이 기반으로 하는 문서를 가리킵니다.

양식, 등록부 및 체크리스트

Verification of Quality Requirements Checklist입력 항목 12개단독으로도 판매Supplier Questionnaire-Quality입력 항목 11개단독으로도 판매Quality Procurement Request Form입력 항목 15개단독으로도 판매Supplier Evaluation Scorecard (Quality)입력 항목 9개단독으로도 판매Quality Risk Assessment Form입력 항목 15개단독으로도 판매Interested Parties Register입력 항목 5개단독으로도 판매Operational Control Register입력 항목 7개단독으로도 판매Infrastructure Responsibilities Register입력 항목 2개단독으로도 판매Objectives Summary Form입력 항목 7개단독으로도 판매Emergency Response Register입력 항목 6개단독으로도 판매Worker Training Record입력 항목 10개단독으로도 판매Outsourced Process Register입력 항목 9개단독으로도 판매Training Needs Register입력 항목 8개참조: Organisation Chart단독으로도 판매Quarterly Objective and Targets Report입력 항목 7개단독으로도 판매Annual Audit Schedule입력 항목 1개단독으로도 판매Roles and Responsibilities Schedule입력 항목 1개단독으로도 판매Operations-Processes – Identification Form입력 항목 3개단독으로도 판매Management Review Meeting Report입력 항목 7개단독으로도 판매Corrective-Preventative Actions Register입력 항목 7개단독으로도 판매Roles, Responsibilities, Accountabilities and Authorities Register입력 항목 6개단독으로도 판매Monitoring and Measuring Equipment Register입력 항목 5개단독으로도 판매AS/NZS ISO 9001:2016 Internal Audit Checklist입력 항목 41개단독으로도 판매Incident Register입력 항목 10개단독으로도 판매Compliance Evaluation Report입력 항목 11개단독으로도 판매Internal Audit Report입력 항목 11개단독으로도 판매Compliance Requirements Register입력 항목 3개단독으로도 판매Risk Register입력 항목 8개단독으로도 판매Communications Program Schedule입력 항목 5개단독으로도 판매Document Register입력 항목 14개단독으로도 판매Non-Conformance Report입력 항목 12개단독으로도 판매Change Request Form입력 항목 16개단독으로도 판매External Quality Control Register입력 항목 7개단독으로도 판매Operational Control Development Worksheet입력 항목 11개단독으로도 판매Objectives and Targets Register입력 항목 5개단독으로도 판매Outsourced Process Schedule입력 항목 3개단독으로도 판매Products Processes – Identification and Material Traceability입력 항목 5개단독으로도 판매Internal Quality Control Register입력 항목 8개단독으로도 판매Worker Training and Induction Register입력 항목 10개단독으로도 판매Training Skills Responsibilities Register입력 항목 8개단독으로도 판매Measuring and Calibration Register입력 항목 5개단독으로도 판매Work Groups Register입력 항목 8개단독으로도 판매Meeting Minutes입력 항목 10개단독으로도 판매Product Approval Checklist입력 항목 8개단독으로도 판매Project Acceptance Criteria입력 항목 7개단독으로도 판매Test Protocols입력 항목 4개단독으로도 판매Monitoring and Measurement Schedule입력 항목 3개단독으로도 판매Corrective and Preventative Actions Form입력 항목 9개단독으로도 판매Quality Incident and Corrective Action Report Form입력 항목 26개단독으로도 판매Monitoring Register입력 항목 7개단독으로도 판매Organisation Chart섹션 5개이 시스템에만 포함Disaster Recovery Response Register입력 항목 8개단독으로도 판매Hazard Report Form입력 항목 14개단독으로도 판매First Aid Worker Register입력 항목 8개단독으로도 판매

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