Login

 

 

 

 

 

 

 

 

 

 

 

Six Sigma

The term Six Sigma refers to the ability of highly capable processes to produce output within specification. Six Sigma actually has its roots in the process capability system. In particular, processes that operate with six sigma quality produce at defect levels below 3.4 defects per (one) million opportunities (DPMO). Six Sigma's implicit goal is to improve all processes to that level of quality or better.

Here's an overview presentation about Six Sigma and is an example of the type of material that is available through this site..

Six Sigma has two key methodologies: DMAIC and DMADV, both formulated at early-adopter General Electric: DMAIC is used to improve an existing business process, and DMADV is used to create new product or process designs for predictable, defect-free performance.

DMAIC - Basic methodology consists of the following five steps:

DMADV - Basic methodology consists of the following five steps:

Some people have used DMAIC-R (Realise). Others contend that focusing on the financial gains realised through Six Sigma is counter-productive and that said financial gains are simply by products of a good process improvement. Six Sigma as applied to product and process design has spawned an alphabet soup of alternatives to DMADV.

The core of the Lean Six Sigma methodology is a data-driven, systematic approach to problem solving, with a focus on customer impact. Statistical tools and analysis are often useful in the process. However, it is a mistake to view the core of the Six Sigma methodology as statistics; an acceptable Six Sigma project can be started with only rudimentary statistical tools.

One of the key innovations of Six Sigma is the professionalization of quality management functions. Prior to Six Sigma, Quality Management in practice was largely relegated to the production floor and to statisticians in a separate quality department. Lean Six Sigma borrows martial arts ranking terminology to define a hierarchy (and career path) that cuts across all business functions and a promotion path straight into the executive suite.

Six Sigma identifies several key roles for its successful implementation.

In many recent programs, Green Belts and Black Belts are empowered to initiate, expand, and lead projects in their area of responsibility.

All tools used in Lean Six Sigma programs are actually a subset of the Quality Engineering discipline and can be considered a part of the ASQ Certified Quality Engineer body of knowledge. The goal of Six Sigma, then, is to use the old tools in concert, for a greater effect than a sum-of-parts approach.

The use of ‘Black Belts’ as itinerant change agents is controversial as it has created a cottage industry of training and certification. This relieves management of accountability for change; pre-Six Sigma implementations, exemplified by the Toyota Production System and Japan's industrial ascension, simply used the technical talent at hand—Design, Manufacturing and Quality Engineers, Toolmakers, Maintenance and Production workers—to optimize the processes.

The expansion of the various ‘Belts’ to include ‘Six Sigma Green Belt’, ‘Master Black Belt’ and ‘Gold Belt’ is commonly seen as a parallel to the various ‘Belt Factories’ that exist in martial arts.

Sigma (the lower-case Greek letter σ) is used to represent standard deviation (a measure of variation) of a population (lower-case 's', is an estimate, based on a sample). The term ‘six sigma process’ comes from the notion that if one has six standard deviations between the mean of a process and the nearest specification limit, there will be practically no items that fail to meet the specifications. This is the basis of the Process Capability Study, often used by quality professionals. The term ‘Six Sigma’ has its roots in this tool, rather than in simple process standard deviation, which is also measured in sigmas. Criticism of the tool itself, and the way that the term was derived from the tool, often sparks criticism of Six Sigma.

The widely accepted definition of a six sigma process is one that produces 3.4 defective parts per million opportunities (DPMO). A process that is normally distributed will have 3.4 parts per million beyond a point that is 4.5 standard deviations above or below the mean (one-sided Capability Study). This implies that 3.4 DPMO corresponds to 4.5 sigmas, not six as the process name would imply. This can be confirmed by running on QuikSigma or Minitab a Capability Study on data with a mean of 0, a standard deviation of 1, and an upper specification limit of 4.5.

In a Capability Study, sigma refers to the number of standard deviations between the process mean and the nearest specification limit, rather than the standard deviation of the process, which is also measured in ‘sigmas’. As process standard deviation goes up, or the mean of the process moves away from the center of the tolerance, the Process Capability sigma number goes down, because fewer standard deviations will then fit between the mean and the nearest specification limit (Cpk Index). The notion that, in the long term, processes usually do not perform as well as they do in the short term is correct. That requires that Process Capability sigma based on long term data is less than or equal to an estimate based on short term sigma. However, the original use of the 1.5 sigma shift is as shown above, and implicitly assumes the opposite.

As sample size increases, the error in the estimate of standard deviation converges much more slowly than the estimate of the mean. Even with a few dozen samples, the estimate of standard deviation often drags an alarming amount of uncertainty into the Capability Study calculations. It follows that estimates of defect rates can be very greatly influenced by uncertainty in the estimate of standard deviation, and that the defective parts per million estimates produced by Capability Studies often ought not to be taken too literally.

Estimates for the number of defective parts per million produced also depends on knowing something about the shape of the distribution from which the samples are drawn. Unfortunately, there are no means for proving that data belong to any particular distribution. One can only assume normality, based on finding no evidence to the contrary. Estimating defective parts per million down into the 100s or 10s of units based on such an assumption is wishful thinking, since actual defects are often deviations from normality, which have been assumed not to exist.