ISO 9001:2015 Certified Lead Auditor Training with Automotive Industry Focus (IATF 16949)
Who Should Attend
Those responsible for planning and scheduling an audit program for ISO 9001:2015/IATF 16949 and those who must perform audits to ISO 9001:2015/IATF 16949, Quality Assurance Managers, Quality Assurance professionals, ISO Project Managers, ISO Project Team Members or anyone desiring an in-depth understanding of the ISO 9001:2015/IATF 16949 Audit Process. This course has been specifically designed to meet the needs of the Auto Industry.
Course Details
• 4 Days
• 3.6 CTUs
• $1695
Upcoming Dates
Course Objectives
- Audit to the ISO 9001:2015/IATF 16949 Quality Management Systems
- Interpret the requirements and terminology of the ISO 9001:2015/IATF 16949 series in a Auto Industry setting
- Develop a ISO 9001:2015/IATF 16949 auditing system based on the ISO 19011 auditing guidelines
- Ask the right audit questions
- Conduct opening and closing meetings that have impact
- Construct effective audit checklists - what to look for in procedures
- Generate effective corrective action
- Plan successful audits
- Select an audit team
- Understand the U.S. and International certification process
- Understand Certified Lead Auditor requirements and responsibilities
- Audit using the Process Approach
- Review documents in light of the decreased emphasis on documentation
- Ask questions that get results
- Identify and document nonconformities
Agenda
- Day One
7:30am to 7:00pm- Terminology and definitions
- Background, History and Rationale for Quality Assurance
- Introduction to the ISO family of documents
- Analysis of the Contents of ISO 9001:2015/IATF 16949 plus;
- Advanced Product Quality Planning and Control Plan (APQP)
- Statistical Process Control (SPC)
- Production Part Approval Process (PPAP)
- Potential Failure Mode Analysis (FMEA)
- Measurement Systems Analysis (MSA)
- IATF Guidance to IATF 16949
- Quality System Assessment Checklist
- Automotive Certification Scheme for IATF 16949
- Audit of Active Manufacturing (Audit #1)
- Day Two
7:30am to 7:00pm- Quality System Requirements
- Analyzing Findings
- Audit of Active Manufacturing to ISO 9001:2015/IATF 16949 and Manual (Audit #2)
- Exemplar Global and U.S. Certification System
- Auditor Qualifications
- Roles and Responsibility of Auditors
- Creation of Effective Audit Checklists
- Day Three
7:30am to 7:00pm- Audit of Company Documents (Audit #3)
- Tips for the Professional Auditor
- Audit of Active Mfg. - Department Audit (Audit #4)
- Compiling Audit Findings
- Documentation in the Quality System
- Planning and Conducting Effective Audits
- Refining Interview and Note-Taking Skills
- Applicability of the Elements to Company Situations
- Prevention vs. Detection
- Day Four
7:30am to 5:30pm
- Audit of Active Mfg. - Dept and System Auditing (#5)
- Corrective Action Initiation and Closure
- Refining Audit Interview and Note-Taking Skills
- Creation of an Audit Report
- Conducting the Audit
- Preparation and Presentation of a Closing Meeting
- Day Five
8:00am to 12:00pm
- Review and Exam
Have questions? Contact us