ENROLL COURSE
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CQI & IRCA Certified ISO 9001:2015 Quality Management System Lead Auditor Training

  • Mode Icon
    Mode
    Virtual Class
  • Duration Icon
    Duration
    40 hrs [5 days]
  • Fees Icon
    Fees
    S$1000
  • Online Assessment Icon
    Online Assessment
    2 Hours

ISO 9001 Lead Auditor Course:

This intensive course is a key requirement in becoming a registered Auditor/Lead Auditor. The course is structured to provide in-depth understanding of QMS requirements (ISO 9001:2015), knowledge and skills required to assess the Quality Management System as an organization.

UTAP grant supported, able to claim up to 50% of course fee.

Note: This course is delivered in association with CQI and IRCA Approved Training Partner.

ATP Number: 01199876 (BSCIC Certifications Pvt. Ltd.)

ISO 9001 Lead Auditor Course

  • A brief discussion upon ISO 9000 Standards series
  • 7 Quality Management Principles
  • Process Approach including the PDCA Cycle
  • Auditing against ISO 9001 Standard Requirements
  • Quality Management System documentation
  • Auditing Standard ISO 19011 requirements
  • Roles and Responsibilities of Auditor
  • Audit Planning
  • Checklists, Non Conformance Reports
  • Audit Reporting
  • Final Team Meeting / Follow-up
  • Verification / Audit Records
  • Accreditation / Certification and Auditor Registration
  • Exercises, case study etc

This course is specially designed for:

  • Quality Professionals/ Consultants
  • Management Representatives/ Managers / Process owners
  • ISO Coordinators
  • Auditors/ Lead Auditors
  • Internal auditors of QMS & Other Management System Standards

At the end of this course, participants will be able to:

  • Describe the purpose, content and relationship of ISO 9000, ISO 9001, ISO 9004 and ISO 19011.
  • Explain the terminology used in ISO 9001.
  • Explain the benefits of third-party certification of a QMS for organizations and stakeholders.
  • Explain the role of the auditor in assessing an organization’s ability to meet customer, statutory and regulatory requirements applicable to the product, and the organizations own requirements

ISO 9001 Lead Auditor Course:

This intensive course is a key requirement in becoming a registered Auditor/Lead Auditor. The course is structured to provide in-depth understanding of QMS requirements (ISO 9001:2015), knowledge and skills required to assess the Quality Management System as an organization.

UTAP grant supported, able to claim up to 50% of course fee.

Note: This course is delivered in association with CQI and IRCA Approved Training Partner.

ATP Number: 01199876 (BSCIC Certifications Pvt. Ltd.)

Next Schedule:
Month Date Duration
August 2026  3, 4, 5, 6 and 7 August 40 hrs [5 days]
September 2026 7, 8, 9, 10 and 11 September
October 2026 5,6,7,8 and 9 October
November 2026 2, 3, 4, 5 and 6 November

ISO 9001 Lead Auditor Course

  • A brief discussion upon ISO 9000 Standards series
  • 7 Quality Management Principles
  • Process Approach including the PDCA Cycle
  • Auditing against ISO 9001 Standard Requirements
  • Quality Management System documentation
  • Auditing Standard ISO 19011 requirements
  • Roles and Responsibilities of Auditor
  • Audit Planning
  • Checklists, Non Conformance Reports
  • Audit Reporting
  • Final Team Meeting / Follow-up
  • Verification / Audit Records
  • Accreditation / Certification and Auditor Registration
  • Exercises, case study etc

This course is specially designed for:

  • Quality Professionals/ Consultants
  • Management Representatives/ Managers / Process owners
  • ISO Coordinators
  • Auditors/ Lead Auditors
  • Internal auditors of QMS & Other Management System Standards

At the end of this course, participants will be able to:

  • Describe the purpose, content and relationship of ISO 9000, ISO 9001, ISO 9004 and ISO 19011.
  • Explain the terminology used in ISO 9001.
  • Explain the benefits of third-party certification of a QMS for organizations and stakeholders.
  • Explain the role of the auditor in assessing an organization’s ability to meet customer, statutory and regulatory requirements applicable to the product, and the organizations own requirements

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