Learn the Failure Mode Effects Analysis (FMEA) Core Tool and help improve your 16949 Quality Management System
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This course is currently available at:
Waterton Training Centre
Waterton Industrial Estate, Bridgend, CF31 3WT
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Confirm the booking.
- IN-HOUSE (At Your Organisation)
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In-company courses can be arranged at your place of work and are extremely cost-effective on a ‘cost-per-attendee’ basis. LMR can tailor this course around your requirements.3 simple steps to get started:
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Confirm the booking.
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- CLASSROOM TRAINING (At One of Our Venues)
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This course is currently available at:
Waterton Training Centre
Waterton Industrial Estate, Bridgend, CF31 3WT3 simple steps to get started:
-
Tell us your requirements
(How many people and any specific requests) -
We will contact you with our proposal and price.
-
Confirm the booking.
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KEY FEATURES
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COURSE OVERVIEW
Learn the Failure Mode Effects Analysis (FMEA) Core Tool and help improve your 16949 Quality Management System
The Automotive Quality Core Tools are the building blocks of an effective quality management system. They include Advanced Product Quality Planning & Control Plan (APQP), Production Part Approval Process (PPAP), Failure Mode and Effects Analysis (FMEA), Measurement System Analysis (MSA), and Statistical Process Control (SPC).
Failure Mode and Effects Analysis (FMEA) is a logical technique utilised to identify and eliminate possible causes of failure. FMEA technique requires a sequential, disciplined approach to assess systems, products or processes in order to establish the modes of failure and the effects of failure on the system, product or process. This is to ensure that all possible failure modes have been fully identified and ranked in order of their importance.
FMEA techniques have been around for over 40 years. In recent years, use of FMEAs has gained popularity as a quality improvement tool. This interest is in large part due to the automotive industry and specifically its IAFT 16949 supplier requirements. Other major industries, including aerospace, medical products and electronics are also using FMEA techniques as part of their improvement and risk assessment strategies. Unlike many quality improvement tools, FMEAs do not require complicated statistics. FMEA studies can yield significant savings for a company as well as reduce the potential liability of a process or product that does not perform as promised.
The FMEA discipline requires the engineers to document their evaluation with regard to the failure mode, effect and criticality (FMECA). The analysis work can be applied at any stage; design, manufacture, test, installation or use, but it is best performed at the design stage.
In a simple system, FMEA may be performed on the total system or product but with more complex systems it may be necessary to break the product down into various sub-systems or sub-assemblies.
Increasingly, contracts are requiring Failure Mode and Effects Analysis (FMEA) to be performed as a condition of placing the order. Also, the use of FMEA minimises the company’s likely exposure to very expensive product liability claims.
FMEA techniques are applicable to all industry sectors, though companies supplying the automotive industry or seeking compliance and registration to ISO/TS 16949, are required to use FMEA techniques to achieve product assurance.
When properly applied the FMEA process can be used to:
Identify or eliminate the potential causes of failure during the product design process, thus speeding up the development process and reducing the number of late changes
Identify critical characteristics of sub-systems and components in a complex product or process
Develop an effective control plan that will reduce the risk of project or product failure due to late delivery and cost overruns
Improve customer satisfaction and reduce warranty costs
This two day practical FMEA training course introduces the principles behind the FMEA techniques and explains how they can be applied at each stage of product and process development. It will provide delegates with a basic knowledge of the FMEA methodology, how to apply it to product and process design, and demonstrate how the results of the FMEA are used to define the requirements for an effective product validation plan, and an effective control plan for the manufacturing process.
*This course can be tailored to your requirements and delivered ‘in-house’ at your premises or in one of our well equipped training venues.
WHO SHOULD ATTEND
- Product developers involved in developing new product introduction strategies and those concerned with ‘time-to-market’.
- Manufacturing and engineering managers who need to improve manufacturing capability, predict initial product yield and improve cross-functional technical communications.
- Design engineers responsible for new product design and introduction who need to improve customer definition and manufacturing feedback.
- Quality/Reliability managers and engineers who want to facilitate an awareness and application of these tools within their organisation.
- Process engineers who will be involved in formulating the manufacturing Control Plan.
- APQP Team Members
- Development Coordinators
- Process Engineers
- Quality Professionals
- PPAP Coordinators
- Project Managers
- Other manufacturing roles related to quality assurance
PREREQUISITES
Those attending this course are expected to have knowledge of the following:
- Participants should have experience working in quality assurance.
- Some experience in ISO-based quality management systems and Control Plan development is also recommended.
LEARNING OUTCOMES
At the successful completion of this course attendees will be able to:
- Explain the benefits and general framework of FMEA as a risk analysis tool
- Explain the purpose of conducting an FMEA.
- Identify the need for completing an FMEA
- Explain the methodology of the FMEA process
- Define FMEA customers
- Assemble an FMEA team
- Identifying the most appropriate Risk Analysis tool to employ
- Relate Process FMEAs to APQP and IATF 16949:2016
- Identify functions, potential failure modes and effects
- Determine potential causes
- Identify current prevention and detection process controls
- Identify improvement opportunities to reduce the risk of failure
- Utilize information gathered from performing an FMEA and construct a Control Plan
- Connect the Process Flow, Process FMEAs, Control Plans and Work Instructions
- Work though each step of conducting a PFMEA
- Use the FMEA Analysis Worksheet to document the results of the study
- Customize the Severity, Occurrence and Detection Ranking Scales
- Be aware of the other Risk Analysis techniques such as; Fault Tree Analysis, Hazard and Operability Studies (HAZOP), Hazard Analysis Critical Control Points (HACCP), PDPC.
- Be capable of interpreting for application purposes the FMEA process
- Be capable of completing an product and process FMEA
- Coherently answer questions regarding the FMEA
CERTIFICATION
Certificate of Completion
WHAT'S INCLUDED
- Detailed course notes
- Certificate of Completion
- Lunch and refreshments
COST
We can offer discounts for corporate clients. Please contact us for a quotation.