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TRAINING COURSE CERTIFICATION (TCC) COURSE REQUIREMENTS Quality Management System (QMS) Internal Auditor Training Course Exemplar Global International Training Certification Programs

Exemplar Global, Inc. is accredited by the Joint Accreditation System of Australia and New Zealand (JAS-ANZ) and InMetro as meeting the requirements of the International Standard for Personnel Certification Bodies, ISO/IEC 17024:2003 General requirements for bodies operating the certification of persons. The Training Certification Programs are not covered under the JAS-ANZ or InMetro accreditations. Disclaimer While every effort is made to ensure that the process for evaluating applications for certification is effective, Exemplar Global, Inc. does not accept liability for the performance, conduct or services provided by the certified person or organisation. Copyright Exemplar Global, Inc. This Training Certification Program and associated Intellectual Property is subject to Exemplar Global, Inc. Copyright. Apart from any fair dealing for the purposes of application, review or reference, as permitted under the Australian and United States of America Copyright Acts, no Page 2

Table of Contents Course Criteria... Pg. 4 Learning Objectives... Pg. 5 Evaluation of Students... Pg. 7 Page 3

Course Criteria 1 General Criteria 1.1 This criteria document is intended for use with TCD62 Training Provider Administrative Requirements and other Exemplar Global Advisories or Technical Advisory Notices. 1.2 No other course may be part of the QMS Internal Auditor course offering. 1.3 The auditor training shall be based on most current revision of ISO 9001 and ISO 19011? 2 Student Pre-Requisites 2.1 No prerequisites required for this course. 3 Course Content, Duration, and Materials 3.1 Early in the course presentation, the training provider shall provide to the students a description of the course format, student responsibilities, how the student will be evaluated, and the basis for each type of evaluation. 3.2 The course shall cover: a) all aspects defined under Learning Objectives; b) local requirements, culture, practices or approaches to auditing and the application of ISO 9001, as appropriate; and c) a reference to the following ISO documents (the contents of which are not required to be covered in the course): 1) ISO/IEC 17021; 2) ISO/TC 176/SC 2/N524. 3.3 The total course time devoted to direct instruction and to assigned team and individual activities shall be at least 23 hours plus at least one hour for examination. 3.4 The course shall be presented during three consecutive days, unless otherwise authorized by Exemplar Global. 3.5 Each student shall have a copy of the current published version of ISO 9001. If the ISO 9001 standard is not supplied as part of the course notes, each student shall be required to bring a copy to the course. A copy shall be made available for loan to any student who does not have one. Page 4

Learning Objectives A student who successfully completes the course shall be able to: 4.1 Standards 4.1 Apply methods for assuring the conformity of the organization s QMS to the requirements of ISO 9001, including conformity to the provisions of QMS documented information; 4.2 Explain the purpose and intent of the ISO 9000 series of standards, how they relate to each other, the concept of the consistent pair of standards as applied to ISO 9001 and ISO 9004, and the terminology used in ISO 9000; 4.3 Describe the eight Quality Management Principles and how they relate to ISO 9001; 4.4 Explain the intent and requirement of each clause of ISO 9001; 4.5 Evaluate the effectiveness of an entire quality management system, including process, customer focus and improvement; 4.6 Describe how the operation planning and control processes and supporting activities can be evaluated effectively in order to verify the degree of conformity and effectiveness of those activities; 4.7 Explain the concept of process-based activities and associated inputs, outputs, controls, and resources; 4.8 Explain the importance of leadership commitment to the QMS; 4.9 Explain the importance of risk-based auditing, e.g. characteristics of quality or hazards related to health and safety, or significant environmental aspects and their control; 4.10 Describe the purpose and intent of management review, internal quality auditing, and monitoring and measuring of the QMS; 4.11 Evaluate, using risk-based thinking, the effectiveness of an entire quality management system, including process, customer focus, and improvement; 4.12 Determine that relevant external and internal issues related to the strategic direction or the organization are monitored and reviewed; 4.13 Describe the difference between legal compliance and conformity with ISO standards, and the significance of these terms when conducting audits; and 4.14 Explain the importance of risk-based auditing (e.g., characteristics of quality or hazards related to health and safety, or significant environmental aspects and their control). Page 5

Learning Objectives 4.2 Audit Process and Responsibilities 4.2.1 Describe the requirements of the current revision of ISO 19011 as applicable to the audit process; 4.2.2 Understand the different objectives of first, second, and third party audits, and the criteria that may be relevant to each type of audit; 4.2.3 Understand the need for independence of the auditor from the work being audited; 4.2.4 Explain the importance of internal audits related to the process of registering an organization s quality management system; 4.2.5 Describe and undertake the roles and responsibilities of an auditor and of an audit team leader during the audit process; 4.2.6 Understand the Exemplar Global certification criteria for QMS internal auditors; and 4.2.7 Understand the Exemplar Global Auditors Code of Conduct. 4.3 Planning the Audit 4.3.1 Explain the importance of scope in relation to: the structure and content of the auditee s QMS, including the concept of application of requirements (exclusions), and the performance of an internal audit (e.g., auditing by department or by process across department boundaries); 4.3.2 Determine the pre-audit information required to effectively plan the duration and the resources required to conduct an audit; 4.3.3 Determine an audit schedule based upon past audit experience and degree of importance based upon the type of business; 4.3.4 Plan and organize all aspects of an audit, including document reviews, in accordance with ISO 19011; 4.3.5 Produce checklists based on process analysis for use during an audit; and 4.3.6 Describe the benefits and risks of the use of checklists during audits. 4.4 Performing the Audit 4.4.1 Perform all aspects of an audit of a process in accordance with ISO 19011; 4.4.2 Manage audit opening and closing meetings and understand the purpose of holding interim meetings with the auditee during the audit in accordance with ISO 19011; 4.4.3 Demonstrate effective interpersonal skills and interview techniques including an ability to listen and question; Page 6

Learning Objectives 4.4.4 Take sufficient notes during the process to provide audit evidence of system conformity as well as nonconformity with the audit criteria; 4.4.5 Explain the risks and benefits of sampling during audits; 4.4.6 Describe how to establish an audit path or trail and when to deviate; and 4.4.7 Collect and analyze evidence during the audit, relate specific audit evidence to the appropriate requirements of the standard and the QMS, and objectively review the evidence collected. 4.5 Reporting and Following Up the Audit 4.5.1 Summarize, record, and present the results of an audit and demonstrate the ability to produce clear and concise reports based on the audit evidence obtained; 4.5.2 Evaluate evidence collected during the audit and prepare reports of conformity and nonconformity to the audit criteria; 4.5.3 Evaluate the significance of nonconformities recorded during the audit and grade them in accordance with the definitions in the audit program (for example: major, minor, observation, etc.). For the purposes of evaluating student competency, the definitions taught during the course shall be used; 4.5.4 Evaluate proposals for corrective and preventive actions prepared by the auditee in response to nonconformities recorded during an audit, evaluate the implementation and effectiveness of corrective actions taken, and evaluate the implementation and effectiveness of preventive actions taken, differentiate between corrective and preventive action; 4.5.5 Make recommendations on the acceptability of a management system for registration based on audit evidence obtained during the audit; and 4.5.6 Describe the roles and responsibilities of the auditor and the auditee at all stages of the corrective action process. Page 7

Evaluation of Students 5.1 Each student shall be evaluated using the following two independent elements, both of which shall be satisfied if the student is to successfully complete the course: The continual evaluation by the instructors of each student s achievement of the Learning Objectives; and An examination that tests students ability to apply audit principles and practices against the requirements of ISO 9001. 5.2 Continual Evaluations The continual evaluation shall be documented and shall evaluate each student s: achievement of the learning objectives; and attendance and punctuality during the course. 5.3 Examination The examination shall evaluate the students' comprehension of the audit process and the application of ISO 9001, and their ability to provide justification of their evaluations. The examination shall be designed so that a competent student (i.e., one who has demonstrated achievement of the learning objectives) could achieve a minimum mark of 70% in one hour. The maximum time allowed for taking the examination shall be two hours. Strict adherence to the time limit shall be maintained. The examination grade shall be based on multiple choice, true/false, and/or short answer (50% minimum short answer/50% maximum true/false, and/or multiple choice) questions that test the student s comprehension of the audit process and the application of ISO 9001, and their ability to provide justification of their evaluation. The exam must include the writing of a nonconformity. The minimum passing grade shall be 70%. The only reference material allowed during the examination are: a) a copy of the ISO 9001 standard, b) the course notes provided by the training provider, and c) any personal notes made by the student during the course. Page 8