Delivering Sustained Success
Countries Regional

CQI & IRCA Certified ISO 9001:2015 Lead Auditor (Quality Management Systems) Training Course (18030)

  • Overview
  • Course Outline
  • For Whom
  • Other Details
  • Related Trainings
CQI & IRCA Certified Course
 
This course is certified by the Chartered Quality Institute (CQI) and International Register of Certificated Auditors (IRCA) and meets the training requirements for initial certification as an IRCA QMS Auditor.

This training is to provide participants with the knowledge and skills needed to fulfil their role as a fully trained Lead Auditor of ISO 9001:2015 Quality Management Systems.

The course includes the 2-stage audit approach for certification of the Quality Management Systems (QMS), in conformity with the ISO/IEC 17021 standard.

This course is aligned to the ISO 19011, the guideline on auditing management systems.


Objectives
This course aims to equip participants with the following knowledge and skills:
  • Knowledge of the purpose of a QMS, of QMS standards, of management system audit, of third party certification and the business benefits of improved performance of the QMS
  • Knowledge of the role and responsibilities of an auditor to plan, conduct, report and follow-up a QMS audit in accordance with ISO 19011 and ISO/IEC 17021
  • Skills to plan, conduct, report and follow-up an audit of a QMS to establish conformity with ISO 9001 and in accordance with ISO 19011 and ISO/IEC 17021.

Benefits
Upon completion of this course, participants will be able to: -
  • Lead and manage 1st, 2nd or 3rd party audits
  • Participate in the planning, preparation, conducting and reporting of audits
  • Present audit findings in a formal and clear manner to the interested parties concerned
  • Assess the effectiveness and adequacy of corrective action taken on audit findings
  • Handle various difficult situations encountered during audits
  • Satisfy the training requirements for initial certification as an IRCA QMS auditor.  The certificate of achievement is valid for three years for this purpose.
Accelerated learning techniques have been incorporated into the course structure to enhance the learning process. Participants are required to actively participate in the group discussions, activities and role plays.  All assignments including performance in simulated/live audit will be assessed.

Day 1
  • Introduction to the course
  • Overview of audits and auditing
  • The audit lifecycle
  • Differences between 1st, 2nd and 3rd party audits
  • Ideal auditor
  • Overview of ISO 9000 series
  • Definitions of key terms used
  • Fundamentals of ISO 9001
  • Audit preparation
  • Documented information and document review
  • Evening assignments: Participants work in teams to prepare for the day 4 “live or simulated audit” exercise
Day 2
  • Auditing the ISO 9001
    • This session draws on the participants’ prior knowledge to audit selected requirements of the standard
  • The audit plan
  • Process risk and performance based auditing
  • Audit checklist
  • Opening meeting
  • Conducting the audit
    • This session provides invaluable information and guidance on how a process-based audit is carried out. Interviewing and information gathering techniques are explained.
  • Evening assignments
Day 3
  • Generating audit findings
  • Reporting and grading findings
  • Closing meeting
  • Corrective action follow-up and surveillance audits
  • International Registration Scheme for Certificated Auditors
  • Exam techniques and debrief on specimen exam paper
  • Evening assignments
Day 4
  • “Live or simulated audit” exercise
    • Participants experience conducting a quality management system audit against ISO 9001 in a “live audit” at an actual organization or in a “simulated audit” exercise.
Day 5
  • Review performance of the “live or simulated audit” exercise
    • The tutor facilitates this session whereby feedback is given on the participants’ performance and any learning points to improve their auditing skills
  • Course review and summary
  • Written closed-book examination (2 hours*)
*Note: additional 30 minute is given if English language is not the particpant’s 1st language.   The ISO 9001:2015 will be provided as reference.


Certificates of achievement will only be awarded to participants who meet the following criteria:
  • Complete/attend all elements of the course
  • Pass the continuous assessment (for class activities)
  • Pass the written examination.
This course is suitable to develop auditors conducting first, second or third party audits. Quality professionals, QMS managers and those interested in furthering their auditing skills will find this a stimulating and beneficial course.


Pre-requisite
Participants must be familiar with the ISO 9001 requirements and the following prior knowledge:

a) Management systems
  • The Plan, Do, Check, Act (PDCA) cycle
  • The core elements of a management system and the interrelationship between top management responsibility, policy, objectives, planning, implementation, measurement, review and continual improvement.
b) Quality management
  • The fundamental concepts and the seven quality management principles (see ISO 9000): Customer focus, Leadership, Engagement of people, Process approach, Improvement, Evidence-based decision making,  Relationship management.
  • The relationship between quality management and customer satisfaction.
c) ISO 9001:2015
Knowledge of the requirements of ISO 9001 and the commonly used quality management terms and definitions, as given in ISO 9000.

The CQI & IRCA recommend participants complete an CQI & IRCA Certified ISO 9001:2015 Foundation QMS Training or equivalent.  Please take note that the written examination questions could relate to the expected prior knowledge.
 
Tutor
The tutor conducting this course has been approved through a vigorous evaluation process based on his skills, knowledge and qualifications. He will be able to share with you his vast audit experience and guide you through the correct application of the ISO 9001 standard in the context of the audit. The tutor will also be able to provide advice on how to handle difficult audit situations.


Duration
This is a five-day course.
Day 1&2: 9.00 am to 7.00 pm – Class work inclusive of evening assignments
Day 3: 9.00 am to 6.30 pm – Class work inclusive of evening assignments
Day 4: 9.00 am to 5.00 pm – Live or simulated audit
Day 5: 9.00 am to 5.00 pm – Class work and two-hour (*) examination  
Full attendance, and passing the examination and practical assessment are compulsory to attain certification.
*Note: additional 30 minute is given if English language is not the participant’s 1st language.  Please take note that the daily timing may be extended depending on the need and progress of the class.


Note for participants from out of town
Participants are encouraged to seek accommodation close to the training venue.  Please be reminded to bring appropriate personal protective equipment for live audit especially covered flat-heeled shoes or safety shoes if available.  Participants are allowed to use a bilingual dictionary during exam therefore participants are encouraged to bring a hardcopy dictionary.  Please take note that electronic devices are not allowed during exam.


CQI & IRCA certification
This course is run by NevilleClarke (ATP 01191057).
Code Title Location
EMS23 CQI & IRCA Certified ISO 14001:2015 Lead Auditor (Environmental Management Systems) Training Course (18040) Philippines
EMS23 CQI & IRCA Certified ISO 14001:2015 Lead Auditor (Environmental Management Systems) Training Course (18040) Indonesia
QMS23 CQI & IRCA Certified ISO 9001:2015 Lead Auditor (Quality Management Systems) Training Course (18030) Indonesia
QMS23 CQI & IRCA Certified ISO 9001:2015 Lead Auditor (Quality Management Systems) Training Course (18030) Singapore
IMS55 CQI & IRCA Certified ISO 9001:2015 Auditor Transition (Quality Management Systems) (17956 & 17957) Philippines
IMS57 CQI & IRCA Certified ISO 9001:2015 & ISO 14001:2015 Auditor Transition (Quality & Environmental Management Systems) (17956, 17957 & 17967) Philippines
QMS07 QMS Audit Report Writing Philippines
QMS12 Measuring & Improving Customer Satisfaction Philippines
QMS20 ISO 9001:2015 Awareness for Top Management Philippines
QMS21 ISO 9001:2015 Interpretation Philippines
QMS22 ISO 9001:2015 Interpretation and Application Philippines
QMS24 ISO 9001:2015 Internal Auditor Training (Process Risk and Performance Based Approach) Philippines
QMS28 ISO 9001:2015 Strategic Approach to Risk-Based Thinking Philippines
QMS29 Supplier Auditing Training Philippines
QMS29 Supplier Auditing Training Philippines
QMS32 TLC Module 2 - QMS Strategic Planning towards ISO 9001:2015 Philippines
QMS33 TLC Module 3 - Documenting & Implementing ISO 9001:2015 Philippines
QMS3X TLC - Training Led Consultancy Towards ISO 9001:2015 Philippines
QMS6305 Process based Approach to Documentation of ISO 9001: 2015 Quality Management System Philippines
QMS6310 QMS Managers (QMR) Skills Development Philippines
QMS6313 Effective Management of Corrective Actions Philippines
QMS6314 Effective Supplier Relationship Management Philippines
QMS6320 Effective Management Review Philippines
QMS6333 Auditing Techniques Enhancement Philippines
 
Available Dates
Philippines, Manila   5 Days
21-25 January 2019
 
Philippines, Manila   5 Days
11-15 February 2019
 
Philippines, Cebu   5 Days
11-15 March 2019
 
Philippines, Manila   5 Days
25-29 March 2019
 
Philippines, Manila   5 Days
22-26 April 2019
 
Philippines, Manila   5 Days
20-24 May 2019
 
Philippines, Cebu   5 Days
17-21 June 2019
 
Philippines, Manila   5 Days
24-28 June 2019
 
Philippines, Manila   5 Days
22-26 July 2019
 
Philippines, Manila   5 Days
05-09 August 2019
 
Philippines, Manila   5 Days
16-20 September 2019
 
Philippines, Cebu   5 Days
07-11 October 2019
 
Philippines, Manila   5 Days
21-25 October 2019
 
Philippines, Manila   5 Days
18-22 November 2019
 
Philippines, Manila   5 Days
09-13 December 2019
 

 

Not ready to register for public training just yet? Want to talk?

"I need more information..."
"I am looking for in-house training..."


If you have any of the above concerns, let's talk!

 

Contact Us