QMS LEAD AUTOR TRAINING COURSES INCLUDING IATF 16949:2016

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Course Information

COURSE INFORMATION It is a long established fact that a reader will be distracted by the readable content of a page when looking at its layout. The point of using Lorem Ipsum is that it has a more-or-less normal distribution of letters, as opposed to using 'Content here, content here', making it look like readable English.

Topic Areas

Manage System, Audit

Assessment

Continious assessment and 2 hours examination

Course duration

5 Days

Reference to existing CQI units/coures

Management System Audit

Course fee

7,000 BAHT

Recommend prior knowledge

ISO 9001:2015

About this course

ABOUT THIS COURSE Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book

 

Our approach

OUR APPROACH The approach that this course will take is based on four factors:

  1.  Formal Approach: lectures with interactions, I talk alittle, you talk a little
  2. Exercise: group exercise with interactive feedback
  3. Delegate assessment: real time
  4.  Basic understanding of the concepts of the course

WHO SHOULD ATTEND?

WHO SHOULD ATTEND It is a long established fact that a reader will be distracted by the readable content of a page when looking at its layout. The point of using Lorem Ipsum is that it has a more-or-less normal distribution of letters, as opposed to using 'Content here, content here', making it look like readable English.

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COURSE OUTLINE

Introduction to ISO 900

  • Quality management system
  • Auditing FMEA
  • Document structure

Auditor qualities & responsibilities

  • Why Audit
  • Auditinfg system
  • Auditing MSA

Auditing planning & preparation

  • Schedule planning
  • Auditing SPC
  • Checklist
  • Opening Meeting
  • Auditing PPAP
  • Conducting the audit
  • Auditing APQP
  • Recording the audit
  • Grading NCR’s

Closing Meeting

  • Corrective Action & Follow up

Future of ISO 9000 and ISO 19011 and IATF 16948

IRCA Registration

Examination

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