IS09001:2000
TS16949:2002
Process Improvement
Six Sigma
EFQM
Health & Safety
Environmental

PROCESS IMPROVEMENT

 

MEASUREMENT SYSTEMS ANALYSIS - (MSA) 2 DAYS

Objectives:

This two-day course is designed to equip delegates with the methodologies applicable to any company that uses measuring devices. The quality of measurement is an important issue for any situation where measurements are used for decision maker purposes and to avoid any unnecessary errors. Delegates will be able to: Help their organisation satisfy TS 16949 : 2002 requirements, help to avoid errors and disputes with customers due to inadequate measurement capabilities, apply suitable techniques to their work processes

Contents:

Formulation of a plan and action plan for applying the learning to their work processes. Reviewing the variation categories of error in a measurement system and covering the methodologies for studying a measurement system such as average and range technique, analysis of variance (ANOVA) and graphical methods. Analysis of results will be taken such as components of variation, discrimination ratio and probable error

 
   

GLOBAL 8DS – PROBLEM SOLVING : 2 DAYS

Objectives:

This course is designed for delegates to understand, describe and participate in this world-class problem solving technique. The course is particularly useful in identifying problems, pitfalls and changes in performance that deviate from the expected level. Delegates will learn to review processes where the root cause can occur and develop an action plan to support the company’s continuous improvement programme.

Contents:

Day 1- Background to Global 8Ds, analysis of the 8D process, model training exercises.

Day 2 – Review of 8D course material, resolving real delegate company problems, exit strategy and final remarks.

 

PRODUCTION PART APPROVAL PROCESS – (PPAP) : 1 DAY

Objectives:

This course is designed for delegates to: Know the purpose of PPAP Systems, have understanding of when PPAP is required, Know the production run and minimum sizes for PPAP sampling, have awareness of the contents of the PPAP file, understand supplier submission levels, appreciate the requirements and retention periods for PPAP records

Contents:

Introduction to PPAP, purpose to PPAP, requirements for part approval, document and sample retention requirements, submission levels, process capability and R & R studies, part submission.

 

STATISTICAL PROCESS CONTROL : 2 DAYS

Objectives:

To provide managers and staff with basic awareness of statistical tools which can be utilised to support ongoing business and process improvement.

Contents:

Calculation of mean and standard deviation, practical application, basic features of probability worksheet, machine capability study – normal distribution and skew distribution, calculation of control limited, completion of X & R process control charts, conclusions: process control attributes, countable data, control chart, conformance criteria, sampling, chart for % defectives, deficient corrections, numbers of defectives, number of defects, defects per item, attribute chart choice, chart interpretation action.

 

FAILURE MODE EFFECT ANALYSIS – (FMEA) : 1 DAY

Objectives:

The course considers the use of FMEA as an analytical tool for engineers to ensure that every conceivable failure of a process or design has been considered, addressed and quantified.
The course uses the thought process of the engineer’s experience based on previous problems and technical knowledge. The technique then provides a framework for formalising and controlling this information once identified and quantified. Using case studies, the following provides a summary of the essential course elements:

Contents:

Process/Design function, frequency of occurrence of failure, failure mode, severity of failure, effects of failure, detection of failure, causes of the failure and calculating risk priority.

 

ADVANCED PRODUCT QUALITY PLANNING – (APQP) : 1 DAY

Objectives:

This course provides the way for suppliers to effectively communicate product quality planning requirements for their sub-contractors.

Delegates will also be able to: Understand the requirements and preferred approaches, appreciate the cost savings of advance planning, relate product quality planning to various TS 16949 : 2002 and production part approved requirements, reinforce the links between FMEA and control plans

Contents:

APQP and control plan manual summary of contents, introduction to product planning factors, organisation requirements for advanced product quality planning and scope of activities, illustration of the methodology and information required to complete a control plan, evaluate and choose critical product and process control characteristics, cost of benefits of accepting improved product planning systems

 
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