In this 2-hour seminar we will walk through the fundamentals of Reverse Process FMEA giving you a sound foundation for what the methodology is, demystify the Reverse Process FMEA by showing you that many of the things included are already being performed inside your organization–just a matter of clearly identifying what the methodology is asking you to do.
Included in the seminar is a basic overview where we look at WHAT exactly this methodology is asking you to do, and WHO is going to ask you to do it. From there we follow a simple example showing the intent and 4 best practices for making your Reverse Process FMEA both effective and efficient.
Once we know what the methodology is, and some simple ways to make it meaningful in your organization, we will cover the integration into the organization’s business management system. This will allow you to maximize the effort you put in the Reverse Process FMEA.
Lastly there will open Q&A on the topic with industry experts, to assist in your understanding and get your individual questions on the topics answered, leaving you confident and informed.
Select an existing open enrollment session, or contact us for additional training options.
Course Length
2 hours + Q&A with the experts
Individuals who complete the course will receive a certificate of completion.
Advanced Product Quality Planning (APQP) and Control Plans reduce the complexity of product quality planning for customers and suppliers by allowing customers to easily communicate their product quality planning requirements to their suppliers.
In this Virtual Seminar Replay participants will experience Plexus technical experts demonstrate application of Design and Process FMEA linkages, learn to create a Process FMEA using information gathered from a Design FMEA, and evaluate consistency of DFMEA and PFMEA linkages.
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?
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