CQI and IRCA Certified ISO 9001:2015 Lead Auditor

Course Objectives

This course will help you:

  • Identify the aims and benefits of an ISO 9001:2015 audit
  • Interpret ISO 9001:2015 requirements for audit application
  • Plan, conduct and follow-up auditing activities that add real value
  • Grasp the application of risk-based thinking, leadership and process
  • management
  • Access the latest auditor techniques and identify appropriate use
  • Build stakeholder confidence by managing processes in line with the latest
  • requirements
  • Meet training requirements for CQI and IRCA certification.

Target Audience

Anyone with the need to audit an organization’s ISO 9001:2015 QMS.

Methodology

You should have a good knowledge of ISO 9001:2015 and the key principles of a QMS. If not, we strongly recommend you attend our ISO 9001:2015 Requirements course. It will also help if you have attended an internal or lead auditor course or have experience with conducting internal or supplier audits.

Course Modules

Day 1

  • Benefits to you, welcome and introductions
  • Course aims, objectives and structure

 

KNOWLEDGE

  • First, second and third party audits
  • Typical audit activities
  • Audit objectives, scopes and criteria
  • Audit resources
  • Roles and responsibilities and confidentiality
  • Audit methods
  • Stage 1 Audit
  • Stage 2 Audit
  • Audit plan template
  • Work documents
  • Opening meeting
  • Audit evidence
  • Effective communication
  • Audit findings
  • Audit meetings
  • Closing meeting
  • Audit reports
  • Audit follow-up
  • Close day 1

 

Day 2

  • Day 1 review

 

KNOWLEDGE continued

  • Purpose and business benefits of a QMS
  • Terminology
  • Plan-Do-Check-Act
  • QMS elements and interactions
  • Role of the Auditor
  • QMS documentation

 

SKILLS

  • Initiating the audit
  • Document review
  • Audit plan
  • Work documents
  • Opening meeting
  • Observations
  • Auditing ‘Top Management’ video
  • Close day 2

 

Day 3

  • Specimen exam: Sections 1 and 2 review

 

SKILLS

  • Auditing ‘Top Management’
  • Auditing ‘Context of the organization’
  • Body language
  • Auditing ‘Planning for the QMS’
  • Auditing ‘risks and opportunities’ video
  • Auditing the organization’s processes (1)
  • Auditing the organization’s processes (2)
  • Close day 3

 

Day 4

  • Specimen exam: Section 3 review

 

SKILLS

  • Auditing the organization’s processes (2)
  • Auditing the organization’s processes (3)
  • Nonconformities
  • Closing meeting
  • Audit report
  • Close day 4

 

Day 5

  • Receive homework – audit report from student
  • Audit follow-up
  • Specimen exam: Section 4
  • The certification and accreditation process, the role of CQI and IRCA, the
  • CQI and IRCA QMS auditor certification requirements and code of conduct
  • Final questions/final revision
  • Evaluation
  • Introduction/readiness to the exam
  • Exam
  • End of course

Get To Know The Trainer

Trainer Irvin

 4.5

Irvin Teh holds a B.Sc (Hons) degree in Computing & Information Systems from the London Guildhall University in the United Kingdom. Throughout the years, Irvin has worked in many corporations and possessed vast Quality, Safety & Health and Environmental experiences.

Trainer Cheong

 4.5

Cheong is a multi-system specialist with more than ten years of proven track records in training, consulting and auditing. An experience and dedicated management system consultant, he possesses extensive hands-on experience in project management; coaching organizations establishing, implementing, maintaining and improving management systems in diversified discipline for Quality, Environmental, Information Security and Energy Management.

Trainer Mabel

 4.5

With a background of Bachelor of Science (Hons) in Computing and Information System from University of Lincoln, Mabel began her career in one of the largest electronics manufacturing multinational organization in Malaysia.

Trainer Joanne

 4.5

With an education background of Applied Sciences and Psychology, Joanne Yip began her career with a plastic resin and film extrusion organization. She then joined a plastic injection moulding organization as Management Representative involving in Quality (incl. Automotive, Medical Device), Environmental, Safety and Health management systems as well as product safety. She had spearheaded the achievement of ISO13485 certification and digitalization of document management system to SharePoint.

  View more trainers

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FREE QUOTATION!

THIS PUBLIC COURSE INCLUDES

Online : 14-18 Jul 2025,18-22 Aug 2025, 22-26 Sep 2025, 27-31 Oct 2025, 24-28 Nov 2025, 15-19 Dec 2025

Physical : 14-18 Jul ; 21-25 Jul, 25-29 Aug ; 11-15 Aug 22-26 Sep, 13-17 Oct, 17-21 Nov ; 24-28 Nov, 15-19 Dec ; 8-12 Dec

*T&C Applies

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