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Statistical analysis of process capability data

Part two of a three part series.

The following is an excerpt from The Quality Engineering Handbook by Thomas Pyzdek, © Quality Publishing. It may be ordered from the Quality Publishing Order Form.

Control chart method: attributes data

1. Collect samples from 25 or more subgroups of consecutively produced units. Follow the guidelines presented in Part 1 of the Process Capability Series, "How to Perform a Process Capability Study"
2. Plot the results on the appropriate control chart (e.g., c chart). If all groups are in statistical control, go to the step #3. Otherwise, identify the special cause of variation and take action to eliminate it. Note that a special cause might be beneficial. Beneficial activities can be "eliminated" as special causes by doing them all of the time. A special cause is "special" only because it comes and goes, not because its impact is either good or bad.
3. Using the control limits from the previous step (called operation control limits), put the control chart to use for a period of time. Once you are satisfied that sufficient time has passed for most special causes to have been identified and eliminated, as verified by the control charts, go to the step #4.
4. The process capability is estimated as the control chart centerline. The centerline on attribute charts is the long-term expected quality level of the process, e.g., the average proportion defective. This is the level created by the common causes of variation.

If the process capability doesn’t meet management requirements, take immediate action to modify the process for the better. "Problem solving" (e.g., studying each defective) won’t help, and it may result in tampering. Whether it meets requirements or not, always be on the lookout for possible process improvements. The control charts will provide verification of improvement.

Control chart method: variables data

1. Collect samples from 25 or more subgroups of consecutively produced units, following the 10-step plan described in Part 1 of the Process Capability Series, "How to Perform a Process Capability Study"
2. Plot the results on the appropriate control chart (e.g., Xbar and R chart). If all groups are in statistical control, go to the step #3. Otherwise, identify the special cause of variation and take action to eliminate it.
3. Using the control limits from the previous step (called operation control limits), put the control chart to use for a period of time. Once you are satisfied that sufficient time has passed for most special causes to have been identified and eliminated, as verified by the control charts, estimate process capability as described below.

The process capability is estimated from the process average and standard deviation, where the standard deviation is computed based on the average range or average standard deviation. When statistical control has been achieved, the capability is the level created by the common causes of process variation. The formulas for estimating the process standard deviation are:

R chart method:

s chart method:

The values d2 and c4 are constants from Table 10 in the appendix of The Complete Guide to the CQM.

Process capability indexes

Only now can the process be compared to engineering requirements. One way of doing this is by calculating "Capability Indexes.’ Here are several popular capability indexes (for normal distributions) and their interpretation.

Z_MIN = Minimum{Z_L, Z_U}

The next article in this series: "Interpreting Capability Indexes"

Follow this link to read Part 1 of the Process Capability Series, "How to Perform a Process Capability Study"