AIAG & VDA FMEA • Live Virtual Workshop

Reverse FMEA for Practitioners

Reverse FMEA is becoming a new requirement mandated by many OEM’s, and appearing in more Supplier Quality Assurance documents. What is it, and more importantly how do I do a Reverse FMEA with all the other checks audits, and details we have to do on a program by program basis?

This 1-day workshop will walk through the fundamentals of Reverse FMEA, giving you a sound foundation for what the methodology is, and demystify the Reverse FMEA process by showing you that many of the things included in the Reverse FMEA are already being performed inside your organization, it is just a matter of clearly identifying what the methodology is asking you to do.

Delivery Options

Choose from our available Open Enrollment dates or request a private training session below.

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Regular Price

Course Description

After we become clear on what the methodology is asking you to do, we will dive into the HOW, and step-by-step complete a Reverse FMEA looking at the activity through the lens of a Process Audit –a very common practice in all manufacturing worlds.

Through connection of the details around the method and the application to your everyday tasks –you will have a sound strategy moving forward to meet the obligation without burdening your organization with additional workload.

Course Details

Length

1 Day (8 Hours)



Prerequisites

none



Required

none



Recommended

Existing knowledge of automotive requirements.

Learning Objectives

  • Identify the key linkages between ISO/TS - IATF 16949:2016 and APQP, FMEA, MSA and SPC
  • Evaluate the 5 phases of APQP
  • Define PPAP submission requirements
  • Design a functional timing plan for production and delivery of a simulated product
  • Name the features of developing a manufacturing system and its control plans, and validating the manufacturing process

Who Should Attend

Recommended for quality managers and quality team leaders, third-party auditors of ISO/TS - IATF 16949:2016, anyone involved in the implementation of ISO/TS - IATF 16949:2016, individuals and cross-functional teams implementing the quality planning process to meet ISO/TS - IATF 16949:2016, and anyone who wants a better understanding of the quality planning process.

Agenda

Day 1

  • Basics of Quality Planning and APQP
  • APQP 1.0 – Plan and Define
  • APQP 2.0 – Product Design and Development
  • APQP 3.0 – Process Design and Development

Day 2

  • APQP 4.0 – Product and Process Validation
  • Production Part Approval Process
  • APQP 5.0 – Production, Feedback and Assessment
  • Key Linkages and APQP Examples
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