Work With Us
Facebook-f
Twitter
Instagram
Whatsapp
ci int de cert logo grayish-01
ONLINE INQUIRY

Training Title

ISO 9001: 2015 Quality Management System Auditor/Lead Auditor Training Course (5 days)

The Course:

  • The course is designed to impart knowledge and skills on organizing, planning and auditing quality system elements to participants.
  • The course covers auditing in the International Quality Management System Standard ISO 9001:2015. Extensive and practical materials will be provided to participants.
  • This course is registered by the Governing Board of The International Register of Certificated Auditors (Registration No.A18185) and meets the training requirements for individuals seeking registration as an Auditor or Lead Auditor under the Scheme.

Learning Objectives

  • Explain the purpose of a quality management system, of quality management systems standards, of management system audit, third-party certification and business benefits of improved performance of the QMS
  • Explain the QMS standards framework of Plan-Do-Check-Act, interrelationship between top management responsibility, policy, objectives, planning, implementation measurement, review and continuous improvement
  • Explain the role and responsibilities of auditor to plan, conduct, report and follow up a QMS audit in accordance with ISO 19011, and ISO 17021, as applicable
  • Plan, conduct, report and follow up an audit of a QMS to establish conformity (or otherwise) with ISO 9001 and in accordance with ISO 19011, and ISO/IEC 17021, as applicable.

    • Who Should Attend?

    • Management representatives and core group members responsible for establishing, implementing, maintaining and auditing Quality Management System (QMS)
    • Quality Professionals, Quality Engineers, Administrators and Executives who wants to improve their Quality Management System
    • Any person involved in organizing, planning and conducting QMS Audit
    • Individuals who want to become registered ISO 9001:2015 Lead Auditor / Auditor

    Prerequisites: Please note that delegates attending this course are required to have minimum level of “expected prior knowledge” in the following areas:
    • Knowledge of Plan, Do, Check, Act (PDCA) Cycle
    • The core elements of a management system and the interrelationship between the top management responsibility, policy, objectives, planning, implementation, measurement, review and continuous improvement
    • Fundamental concepts and quality management principles
    • The relationship between quality management and customer satisfaction
    • Knowledge on ISO 9001 requirements and commonly used terms and definitions
    Delegates that are not familiar with the purpose and intent of the ISO 9001 should complete an IRCA Certified QMS Foundation Training course or equivalent

    Course Programme

    Session 1: Course Introduction

    Session 2: Introduction to Quality Management System

    Session 3: ISO 9001:2015 Requirements

    Session 4: Audit Principles and Managing an Audit Programme

    Session 5: Planning the Audit

    Session 6: Conducting the Audit

    Session 7: Generating audit findings

    Session 8: Reporting and Following up the audit

    Session 9: Certification Process and IRCA Registration

    Methodology

    Accelerated learning through workshops, role play, discussion, mock audit and presentation.

    Duration

    5 days (0900 – 1800 hours)

    Training Date

    11-14 & 16 May 2022

    Application Form

    Fee Per Participant

    RM3800 + 6% SST
    Our Services
    ISO9001 Quality Management System
    ISO 37001 Anti-Bribery Management System
    ISO 14001 Environmental Management System
    ISO 41001 Facilities Management System
    ISO 45001 Occupational Health & Safety Management System
    ISO 22000 Food Safety Management System
    ISO 27001 Information Security Management System
    ISO 20000 Information Technology Service Management System
    ISO 50001 Energy Management System
    ISO 28001 Security Management System for the Supply Chain
    ISO 13485 Medical Device Quality Management System
    GDPMD Good Distribution Practice for Medical Device
    HACCP Hazard Analysis and Critical Control Point
    GMPs Good Manufacturing Practices
    MS 2530 (Part 1-4) Malaysian Sustainable Palm Oil (MSPO)
    Integrated Management System (IMS)

    CI International Certification Sdn Bhd
    CIMY International Standards Training (M) Sdn Bhd

    Send a Message

    Send a Message