QUALITY
• MSA elements
AS13004: Process Failure Mode and Effects Analysis (PFMEA) and Control Plans 2 Days | Classroom Seminar I.D.# C1889 In the Aerospace Industry there is a growing focus on Defect Prevention to ensure that quality goals are met. Process Failure Mode & Effects Analysis (PFMEA) and Control Plan activities described in AS13004 are recognized as being one of the most effective, on the journey to Zero Defects. This two-day course is designed to explain the core tools of Process Flow Diagrams, Process Failure Mode & Effects Analysis (PFMEA) and Control Plans as described in AS13004. It will show the links to other quality tools such as Design FMEA, Characteristics Matrix and Measurement Systems Analysis (MSA). The course will include hands on examples of PFMEA deployment in a variety of typical manufacturing environments (including processing, machining and assembly) to illustrate how the technique is to be deployed. It will also describe the use of Reference Process FMEAs that can be used to minimize the duplication and reduce the time taken to produce an effective PFMEA whilst maintaining the required rigor. • Evaluate and contribute to the Design FMEA activity • Complete a Process Flow Diagram (PFD) in line with AS13004 requirements • Lead the development of a Process FMEA on a manufacturing / assembly process • Assess Process Risks and prioritize actions • Identify appropriate risk mitigation improvement actions • Learn how to develop a Control Plan from the Process FMEA information • Create Reference Process FMEAs for future use in creating Part Specific PFMEAs • Set out a deployment strategy for your business for AS13004 Topical Outline DAY ONE • Introduction −− Scope & purpose of the AS13003 Standard Learning Objectives By attending this seminar, you will be able to:
−− Design factors −− Analysis of results −− Mitigation strategies for failed results −− Environmental factors −− Use of red across results in MSA
DAY TWO • MSA process flow
−− MSA process flow −− Appropriate gage selection −− Variation analysis −− Analyze results and take action • Audit checklist for MSA • MSA case studies −− First case study −− Second case study
−− Third case study −− Fourth case study −− Fifth case study
Instructor: Fee: $1415
Suzanne Hill
1.3 CEUs
URL:
sae.org/learn/content/c1889/
AS9100D Internal Audit Program Implementation 3 Days | Classroom Seminar I.D.# C1713
One of the most important requirements for AS9100 series and other quality standards, is to create, implement and maintain an effective Internal Audit Program. An improperly designed and implemented Internal Audit Program could result in non-conformances leading companies to improperly identifying and describing non-conformances, applying incomplete or inadequate root cause analyses, establishing ineffective corrective actions, implementing incomplete Internal Auditor Qualification Programs, etc. A well-developed auditing program enables the monitoring of and improvements to the effectiveness of the Quality Management System (QMS) which will reduce risk and cost of non-conformances. This unique three-day seminar will cover how to create, implement and maintain an effective Internal Audit Program, including the preparation, the follow-up and closure of the internal audit and an internal auditor qualification program. The information presented in this seminar is related to the AS9100D Internal Auditor Training course but extends to the entire Internal Auditor Process including creation, implementation, and sustainment.
−− Applicability −− Types of data
• Attribute data • Variable data −− Overview of Measurement system analysis (MSA) −− Organization and competence requirements −− Quality System • Measurement system analysis requirements
−− Pre-requisites −− Considerations −− Minimum requirements
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3 ways to get a no-obligation price quote to deliver a course to your company: Call SAE Corporate Learning at +1.724.772.8529 | Fill out the online quote request at sae.org/corplearning | Email us at Corplearn@sae.org
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