Professional Documents
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Error Elimination
Error Elimination
Error elimination
Q: What’s the best way to reduce human
error in production?
Submitted via the QP reader survey
8 QP • www.qualityprogress.com
rs
An emphasis on doing it right the first time
can play a key role in reducing human errors.
• Designing nonsymmetrical parts. Conformance question other auditing body. Some auditing bodies
• Creating features such as drill or dowel Q: Recently, a new firm began auditing our will follow up on closed corrective action
holes to prevent variations in a sym- organization, and I’m noticing differences in reports during their next scheduled surveil-
metrical assembly. requirements compared with our previous lance audit. This allows enough time for the
• Designing fasteners of the same thread auditor. At the closing of an annual surveil- organization to evaluate the effectiveness
size to prevent the application of incor- lance audit for a three-year certificate, if a of the corrective action taken.
rect torque. nonconformance is issued at the closing In most cases, the auditee is required
• Designing parts that combine two ele- meeting: to complete the correction action report
ments—such as a washer head and a • What is the expectation for response to identifying the root cause and the cor-
screw.2 the auditor for a minor nonconformance rective actions taken to prevent a recur-
The initial cost of developing a system to and a major nonconformance? rence. This information is assessed by the
prevent errors may be low or high depend- • How many days are expected for the auditing body to confirm that a root cause
ing on the situation. You will need to weigh initial response for each? was identified and that the action taken
the severity and probability of the error to • How many times during the next 12 matches the root cause. This is normally
justify the need. months should we expect the auditor to done in the form of a desk review.
For situations in which it is cost prohibi- revisit the site to verify corrective action Due to the costs involved and other
tive to design a system to prevent errors, for each? logistics, it’s rare for any auditing body to
you can use a qualified and competent em- Deborah Magoon want to come out to verify each corrective
ployee with the right attitude to significantly Grand Rapids, MI action taken. This is usually something for
reduce those errors. the internal audit staff to perform as part of
Besides designing a system to prevent A: Clause 8.2 of ISO 9001:2008, internal its audit activities.
errors, it’s possible to reduce the num- audits, does not specify or prescribe any Bill Aston
ber of errors if the workload is planned time limits. Clause 8.2.2 only requires the Managing director
in a way that distributes it evenly among management for the responsible area—the Aston Technical Consulting Services
your employees, thus reducing stress and process owner—to take corrective action Kingwood, TX
fatigue. without undue delay.
Organizational culture and an overall With regard to audit follow-up visits, Bibliography
International Organization for Standardization, ISO
emphasis on doing it right the first time this depends strictly on the registrar or 9001:2008—Quality management systems—Requirements.
February 2012 • QP 9