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Exemplar Global Certified ISO 9001:2015 Lead Auditor Training (RTP)

** Onsite classes will be added to the schedule for 2022 as COVID-19 Health concerns allow.
For classes onsite at your facility contact QUAL-TECH directly.

DateLocationCourse
December 5th - 9th, 2022VirtualExemplar Global Certified ISO 9001:2015 Lead Auditor Training (RTP)​
January 30th – February 2nd, 2023VirtualExemplar Global Certified ISO 9001:2015 Lead Auditor Training (RTP)​
February 6th – 10th, 2023VirtualExemplar Global Certified ISO 9001:2015 Lead Auditor Training (RTP)​
May 8th – 11th, 2023VirtualExemplar Global Certified ISO 9001:2015 Lead Auditor Training (RTP)​
July 31st – August 4th, 2023VirtualExemplar Global Certified ISO 9001:2015 Lead Auditor Training (RTP)​
September 11th – 15th, 2023VirtualExemplar Global Certified ISO 9001:2015 Lead Auditor Training (RTP)​
October 2nd – 6th, 2023VirtualExemplar Global Certified ISO 9001:2015 Lead Auditor Training (RTP)​
November 6th – 10th, 2023VirtualExemplar Global Certified ISO 9001:2015 Lead Auditor Training (RTP)​
December 4th – 8th, 2023VirtualExemplar Global Certified ISO 9001:2015 Lead Auditor Training (RTP)​

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Who Should Attend:

Anyone involved in planning, scheduling, and conducting ISO 9001 internal audits. Personnel leading their companies toward ISO 9001 Certification, top management, quality, engineering, internal auditing, production, purchasing, customer service, accounting, shipping and receiving, sales, ISO Project Team Members or anyone desiring an in-depth understanding of ISO 9001 requirements. This course satisfies the training requirements for Quality Management System (QMS) Third-Party Auditors. In addition, this course is the first part of the Aerospace Auditor Training Requirements for AS9100:2016 Third Party Auditing. Together with successful completion of the IAQG Sanction AATT 9100 Training; all training requirements are met to be a Third Party Aerospace Auditor.

Course Objectives:

  • The new requirements of ISO 9001:2015 and the impact to the audit process.
  • How to audit ISO 9001:2015 specifically the requirement for documented information and the impact for auditors when audit evidence may be more difficult to determine.
  • How to audit Risk Management (Risk Based Thinking).
  • How to audit Organizational Knowledge.
  • The requirements of the Quality Management System (QMS), business objectives, and auditor’s ability to assess the business processes and results.
  • Methods on how Top Management can demonstrate ownership for the QMS.
  • Documented information requirements.
  • Methods for the identification of the needs and expectations of interested parties.
  • Determining interested parties.
  • Needs and expectations the organization needs to consider.
  • Incorporating the needs and expectations of interested parties into the organizations QMS.
  • Requirements to transition the current QMS to ISO 9001:2015.
  • Methodologies to address “Risks and Opportunities” (Risk Based Thinking).
  • Methodologies to address “Organizational Knowledge.
  • Plan, manage, and conduct an audit effectively.
  • Understand the roles and responsibilities of auditors.
  • Recognize the principles, practices, and types of audits as well as the objectives, scope, and criteria in the audit process.
  • Conduct audit team selections and understand Team Lead Responsibilities.
  • Understand how to communicate effectively – and the level of communication required during audits.
  • Prepare audit conclusions.
  • Conduct a closing meeting.
  • Report audit results.

Time:

Day 1: 8:00 a.m. – 6:30 p.m. Day 2: 8:00 a.m. – 5:30 p.m. Day 3: 8:00 a.m. – 6:45 p.m. Day 4: 8:00 a.m. – 7:15 p.m.

On Site: $1,865.00
Virtual: $1,305.50

Any of the ISO standards can be integrated with each other for $1965.00 (On-Site) & $1375.50 (Virtual)

Agenda

Day One

  • Course objectives and overview
  • Review of acronyms, definitions, ISO documents
  • PDCA, Process Overview, ISO 9001:2015 standard comprehensive and detailed review of the standard including a discussion of the requirements of each clause, internal and external (3rd party) interpretations and application during the audit process.
  • Activity # 1 Status of Audit Findings
  • Discussion of Activity # 1

Day Two

  • Review of ISO 19011, ISO 17021 and MD-5
  • Activity # 2 Preparing an audit plan
  • Discussion of Activity # 2
  • Review of ISO 19011, ISO 17021, and MD-5 (cont)
  • Effective Process Auditing
  • Process Tools

Day Three

  • Activity # 3 Developing an Audit Process Tool
  • Discussion of Activity # 3
  • Activity # 4 Opening Meeting
  • Discussion of Activity # 4
  • Activity # 5 Phase I – Desk Audit: development of potential audit trails and concerns
  • Activity # 5 Phase II – Conduct audit #1 & # 2
  • Activity # 5 Phase III – Team review of audit results and conclusions

Day Four

  • Nonconformance generation and audit reporting
  • Activity # 6 Nonconformance Generation
  • Activity # 7 Closing Meeting
  • Activity # 6 and # 7 discussion
  • Auditor certification and Certification/Registration Requirements
  • Exam

Re-Takes

To be scheduled with headquarters

QUAL-TECH INC.

Orlando, Florida

6900 Tavistock Lakes Blvd.
Suite 400
Orlando, FL 32827

Mill Spring, North Carolina
82 N Highway 9
Ste 3
Mill Spring, NC 28756

IAQG Sanctioned, Probitas Certified & Exemplar Global Certified Lead Auditor Training

Cage Code: 4DND0

(321) 453-0637
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THANK YOU!

We’ve received your registration request.
We’ll be contacting you soon about this event, payment details, and additional information.

Final registration and payment arrangement is completed directly with QUAL-TECH INC Headquarters.

For immediate questions or to make a payment, you can contact QUAL-TECH INC by calling 321-453-0637.

Regards,
QUAL-TECH INC Team