January 27, 2021 | Lean Manufacturing

# Six Sigma Principles and Tools

Welcome to the third installment of our series on Lean and Six Sigma. As we saw in the first post, "What Are Lean & Six Sigma Methodologies?", Lean and Six Sigma are complimentary continuous improvement methodologies that reduce the overall waste and variability in production processes respectively. The second post, "Lean Principles and Tools," went into some depth on a few of the key principles, tools and methodologies in Lean. Here we conclude our series with a high-level discussion of Six Sigma. There are many tools in the Six Sigma toolkit (Failure Mode Effects Analysis (FMEA), IPO Diagram, Confidence Intervals, Histograms, Pareto Charts, F-Tests, Design for Six Sigma (DFSS), and many more) that will not be discussed here. The focus here is to discuss the statistical realities that make Six Sigma effective.

Six Sigma aims to identify and eliminate the root cause(s) of defects and waste using statistical tools to identify the variations causing defects. In Six Sigma methodology, the only way to effectively solve a problem is to permanently eliminate its root cause.

It is a measurement-based strategy that focuses on process improvement striving to achieve not more than 3.4 defects per million opportunities. A Six Sigma defect is defined as anything outside of customer specifications. A Six Sigma opportunity is then the total quantity of chances for a defect to occur.

**Six Sigma Doctrine**

Six Sigma is based on three key ideas that comprise the Six Sigma Doctrine:- Continuous efforts to achieve stable and predictable process results (i.e., reduce process variation) are of vital importance to business success.
- Manufacturing and business processes have characteristics that can be measured, analyzed, controlled and improved.
- Achieving sustained quality improvement requires commitment from the entire organization, particularly from top-level management.

Six Sigma Methodology: The DMAIC Process

DMAIC is a Six Sigma problem-solving methodology that is driven by data. The five-phase process is described by each letter of the acronym:

**Define**- Describe the problem, project goals, areas of improvement, or customer requirements.**Measure**- Measure process performance.**Analyze**- Analyze and identify possible root causes for defects and variations.**Improve**- Improve operations by eliminating the root causes.- Control - Quality control the improvement process.

*Let's break the phases down further:*

### Define

Once the problem, goal, or area of improvement is described, it is critical to attempt to identify the various input and output variables that are related to the behavior of the process. Often the output variables are the one(s) that are out of the specifications. It is important to identify which input variables can be causing the variation with the output variable(s).

### Measure

Once the input variables that are causing the output behavior are identified, it is possible to develop a measurement plan that provide enough data to start the analysis. This phase is where data is collected on the key input and output variables. This is also the phase where performance baselines are developed for use in measuring the improvements made later. As a rule, at least 30 observations are required to provide enough data to represent the process behavior.

### Analyze

Once the data is collected, it is analyzed to determine the most likely three to five potential root causes. This is accomplished by continued data collection and review to understand the contribution of each potential root cause using statistical tools, plots and charts. The DMAIC process is iterative and repeats until all valid root causes are identified.

### Improve

Based on the valid root causes identified in the Analyze phase, the process is adjusted until the excessive variation is eliminated. The Measure and Analyze phases are repeated until the desired outcome is achieved.

### Control

When the desired outcome is achieved, the improvements are institutionalized so that the source of the excessive variation is eliminated. This step should be accompanied by a control plan to ensure that the outputs continue to be at an acceptable quality level. The Control Plan includes implementing Statistical Process Control to monitor the process and ensure that it continues to function properly over time. This control plan should also include countermeasures if a problem occurs.

**In Summary:** DMAIC is a problem-solving methodology that helps the practitioner approach a problem with excess variation and systematically solve it.

## Statistical Process Control

Statistical Process Control is a tool that measures whether or not a process is meeting product or process standards. If a process is capable and stable over time, the outcomes that the process was designed to produce will be achieved.

Let’s use an example to better understand these important concepts. Think about baking muffins.

### Process Capability and Variation

A process is transforming inputs into outputs. In this case, the ingredients are the inputs. It is known that the oven needs to reach a given temperature for a specific amount of time with the muffin batter inside to get the ideal muffins.

Let’s assume that the oven is working correctly. It is capable of producing what we want - warm muffins baked exactly and perfectly. Does the fact that the oven is working correctly guarantee that the baked goods will come out right?

Of course not.

What if the oven is working correctly, but one's muffin-starved, anxious children keep opening the door to see if the muffins are done yet? The muffins will turn out only half-baked when the timer goes off. This is an example of a special cause of variation — we are not getting the desired outcome because the process is out of control. The process is capable, it will give us what we want when it is employed properly, but it is not in control.

If we ensure the oven is working optimally — at the right temperature and with the oven door *closed* for the prescribed time — the process will be back into control. We now have a process that is both capable and in control, and we can reasonably expect it to produce an ideal dozen muffins.

If all special causes of variation as above have been eliminated, then the process is deemed in control and all of the variations that are experienced are variations that are inherent to the process itself. These include small variations in measured ingredients and slight variations in oven temperature. But, the process is robust enough to produce the desired outcome even with these sources of (inherent) variation.

**In Summary: **Process Capability is a measure of how capable the process is to produce the desired outcome — i.e., it can tell us what percentage of defects the process will inherently produce if it is in control. Desired outcome: a dozen perfectly baked muffins.

### Standard Deviation

Now that you know how to bake the ideal muffin, we’ll introduce Standard Deviation.

Standard Deviation (Ϭ) is a measure of variation and the number used to calculate Process Capability. It is calculated as the square root of the variance.

Dr. William Shewhart, the Father of Quality, began developing control charts in the early 1920s. He realized that if key process output variables were measured, and they created a distribution that would graph like the bell-shaped curve above, then the variation being displayed was random and, therefore, inherent to the process.

In other words, the process is behaving or operating in the manner it was designed to work. If the data is not random, then there must be a logic to explain that behavior. That is what a special cause of variation is.

Then there’s the Empirical Rule. This rule tells us that, for a Random Distribution:

- 68% of the observations will be within plus or minus 1 Standard Deviation
- 95% of the observations will be within plus or minus 2 Standard Deviations
- 99.7% of the observations will be within plus or minus 3 Standard Deviations

Shewhart also designed control charts (see below) that include control limits. Control limits are usually a distance of plus or minus three Standard Deviations from the mean. And, we know that if the data points are within the control limits, then our quality level is at least 99.7% good.

Statistical Process Control uses this knowledge to an advantage. Two graphs (run charts) are monitored by entering data and observing where the data points are located relative to the mean (average) and the control limits. As long as the plots fall within the control limits, then the process is deemed to be in control. So, for the muffin example, the run chart on oven temperature would show the special cause of variation in temperature due to the frequent opening of the oven door as outside of the normal range — the normal range of variation being from the random temperature variation as the heat source in the oven turns on and off for instance.

Please notice that there is no attention paid to the specifications or specification limits (tolerances). A process that is in control is producing what it was designed (not necessarily intended) to produce. Thus, it may actually be producing bad outputs.

### Process Capability Index and Controls

In Six Sigma, the Process Capability Index (Cpk) is a statistical tool used to measure the ability of a process to produce products within a client’s tolerance range. The higher the Cpk, the narrower the process distribution compared to the tolerance range, and the more uniform the output.

Cpk is calculated using the following formula, where UCL refers to the upper control limit and LCL refers to the lower control limit:

**Cpk = min(UCL - μ, μ - LCL) / (3σ)**

The higher the Cpk, the better (closer to 2.0 is excellent) where a Cpk of 1.33 essentially indicates the lowest value for a process that is in control and meets specification.

By now we know if a process is capable and in control, it will, by definition, produce the outcome that the process was designed to produce. We discussed how to measure Process Control with SPC and the importance of keeping a process in control.

The specification limits relate to the process’s tolerances. For instance, a screw could be dimensioned to be 3 inches (3”) in diameter. But, how do we accommodate the inherent variation in the process to produce the pin? We do that by providing tolerances. It is determined that a screw of 3”, plus or minus three-thousandths of an inch (.003 inch) in diameter, is good enough. All screws within that range of diameters will work successfully for its application.

According to NIST (National Institute of Standards and Technology):

“Process capability compares the output of an in-control process to the specification limits by using capability indices. The comparison is made by forming the ratio of the spread between the process specifications (the specification “width”) to the spread of the process values, as measured by 6 process standard deviation units (the process “width”).”

The Process Capability Index is used to determine how close the output is to the existing target and how consistent average performance is. Therefore, it can be used to predict future output performances and consistency.

## Process Capability Index And Standard Deviation

For our purposes, all we need to know is that we can determine the ability of a process to produce good parts. This is the same as answering the following:

- What percentage of the output will meet the customer’s specifications?*
- How many screws will be larger than the 3 inches plus the three thousandths in diameter (3.003 inches)?
- How many screws will be smaller than the 3 inches and less than three thousandths in diameter (2.997 inches)?

You may remember that:

The three Standard Deviation measures of variation signify a quality level of 99.7% of good work produced. This is the equivalent of a Process Capability measure of one.

**The literature is pretty much in agreement:**

We need a Process Capability (Cp and Cpk) measure of at least 1.33.

This allows for what is known as shift and drift where the normal variation of the process causes some defects that would not occur if there were no variation.

But there will always be variation. The key is to maintain good process control to avoid defects.

**Again, according to NIST:**

“A process capability index uses both the process variability and the process specifications to determine whether the process is ‘capable’.”

## Shift & Drift

The main issue in maintaining good process control is that, over time, any process will shift and drift, no matter how tight the initial settings were. When this occurs, the key point to remember is that as the process average moves, so does the entire variable range, while the specification limits stay stationary.

If the process moves beyond the specification limits, the process will be making defective products. You want to maintain index levels of 1.00 or better. This is achieved with good centering of the process average and minimizing variability.

**In Summary:** Using Six Sigma, it is possible to understand if a process is capable and to measure Process Control and Process Capability. As long as an "in control" process is capable of producing the desired outcome (Process Capability Cpk of at least 1.33), then it must perform properly as long as it is in control. For more information about Six Sigma, or Lean, please visit www.cmtc.com and select the "Services" option.

## Who We Are At CMTC

CMTC offers technical assistance, workforce development, and consulting services to small and medium-sized manufacturers (SMMs) across California to help SMMs increase their productivity and global competitiveness.

For more information about CMTC, visit our website at www.cmtc.com or contact us at 310-263- 3060.

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