100%

QMS Lead Auditor Training Course inc IATF 16949:2016 Automotive Quality Management (CQI-IRCA :ID 1839) 5 day Course (day 1 & day 2)

Warning: Invalid argument supplied for foreach() in /home/robere/public_html/wp-content/themes/elumine-child/content-single-public_courses.php on line 11

QMS Lead Auditor Training Course inc IATF 16949:2016 Automotive Quality Management (CQI-IRCA :ID 1839) Day 1 & Day 2

Course Duration

5 day

Course Fee

27,000 Baht per person (Excludes 7% VAT)

Start Date

Course Description

This course is designed to provide those in the automotive industry specific information about how to plan, prepare, conduct and report the audit of IATF 16949. Additional information is provided to understand what the specific areas of APQP are, PPAP, FMEA, MSA should be reviewed to ensure that their company or their suppliers are fulfilling specific requirements

WHO SHOULD ATTEND?

Anyone responsible for leading the audit, satisfying the training requirements for becoming a certified Lead Auditor for ISO 9001:2015 and qualified Lead Auditor for IATF 16949:2016, or anyone interested in being educated with the most comprehensive course on ISO 9001:2015 or IATF 16949:2016 auditing technique.

PREREQUISITES

All participants should have a basic understanding of ISO 9001:2015 or IATF 16949:2016 requirements and have participated in the ISO 9001:2015 or IATF 16949:2016 Quality Systems

HOW YOU WILL BENEFIT?

At the end of this course, the participant will be able to:
• Successful completion of this course satisfies the training requirements necessary for registration of individual auditors under the CQI-IRCA
• Gain the knowledge and skills of quality systems auditing
• Receive “hand-on” training from one of the most experienced and respected ISO 9001 and IATF 16949 training companies in the world
• Become an authority on ISO 9001 and IATF 16949 and guide your company to a leadership position as you improve your business practices.

COURSE OUTLINE

Session 1

• Introduction to ISO 9001 and IATF 16949
• Quality Management System Overview
• ISO 9001 and IATF 16949 Standards
• Auditing FMEA
• Document Structure
• Auditor qualities & responsibilities
• Why Audit
• The Audit System
• Auditing MSA
• Audit Infrastructure
• Audit planning & preparation
• Schedule planning

Session 2

• 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 16949
• CQI-IRCA Registrations
• Examination

DAILY SCHEDULE

Registration will take place at 9:00 a.m. with the course running from approximately
9:30 a.m. – 5:30 p.m. Break time is 10:00 a.m. and 3:00 p.m.

INTERESTED?