LPA - Layer Process Audit Guidelines
LPA - Layer Process Audit Guidelines
Why LPA’s?
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What do you want this program to
deliver?
• What are LPA’s good at addressing?
– Repetitive issues involving known solutions
– High risk / liability items involving known solutions
– Items easily verified without special training
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Possible Targeted Items
• Safety
– Proper PPE / Guarding
– Completion of required daily inspections
• Morale
– Bring focus and voice to operator issues/concerns.
• Cost
– FTQ goals
• Quality
– Proper product identification
– Error proofing verification (i.e. the rabbit test)
– Improved work standardization
– Calibration
– Training
– Control of Non-conforming Product
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Key Items for Success
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Benefits
• Reduced OSHA injury rates
• Improved DMR rates
• Increase ability of detecting product or
process problems internally
• Highlighted variances in set-ups and driving
to improve standardization
– Training gaps identified
• Verification that process controls are being
followed
• Bring all areas of the organization into
operations
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Definition
• Layered Process Audits is a process to ensure
compliance to procedure for shop floor standards
and standard work
• It is a series of audits done by multiple layers of an
organization to reinforce standards and standard
work
• The audits are completed by levels up to and
including top plant management
• Results of these audits are measured for
completion % and compliance %
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Why do we do layered process
audits?
• Ensure key procedures are being followed
• Instill the importance of following procedures on
the shop floor
• Monitor the execution of corrective actions
• Ensure a high level of process control by
identifying &controlling high risk/significant
process elements
• Identify opportunity for improvements and provide
a process for effective follow up
• Encourage people involvement in quality,
leadership and shop floor
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How LPA’s link in the Quality System
– Quality
• Ensure the corrective action for previous quality issue is in
place and functioning as desired
– Error Proofing Verification
• Ensure the EPV is being used and is working
– Control of Non-Conforming product
• Ensure specific CNCP procedures are being followed
– Standard work
• Ensure work being done to established standard
– Process control
• Check process control compliance to PCP
– Fast Response
• Entry criteria to FR as well as a exit criteria
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Minimum Requirements
Additional Comments/Observations:
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Minimum Requirements
Executive
Managers
/ Directors
As
Quarterly
available/
minimum
• Every shift
Plant
Plant
Manager
staff – Team leader
1 1time
time/week
/ month
• Weekly
– Department supervisor
Dept.
Managersupervisor/mgr
/ Engineers
21 times/week
time/week
• Weekly
– Plant staff member
Supervisor
Team/ Team
LeaderLeader
Daily
Every
/ Weekly
Shift
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Minimum Requirements
All auditors must have backup (to consistently complete all scheduled
audits regardless of absences).
Audit content is owned by manufacturing. Audit system is facilitated by
Quality
All upper level audits (above lowest level) are reviewed with the department
representative immediately following the audit.
Best practice: audits are completed with department representative
(department manager, team leader, LMA).
Who
Best practice: other pre and post production operations are included in LPA
process and audited (shipping, production control, engineering, launch
processes, receiving inspection)
.
Additional Comments/Observations:
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Step by step-Develop a checklist
A list of high risk items to be verified during Layered Process
Audits shall be established. Minimum elements to include
are:
– Gages functioning and calibration confirmation
– FTQ
– Past corrective actions and repeat issues.
– Process parameters
– Work instructions
– Training effectiveness
– Product identification / control of non-conforming product
– Documentation/record completion
– Customer feedback
– Error Proofing Verification
Layered Process Audits shall verify appropriate Quality
documentation. Always think about high risk items!
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Step by step
• Develop LPA work instruction and form
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Example Audit Questions
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Example Audit Questions
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Example Audit Questions
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Audit Questions
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Step by Step- Conduct audit and
display the results
LPA results must be visible at the location being audited (line or
department)
There is a consistent audit form (single audit documentation) throughout
the plant **
There is a consistent audit findings visual display (one week audit
summary) in each department throughout the plant **
Findings identified with consistent marking
O = conforming
Format
X = nonconforming
? = nonconforming but corrected
All LPA corrective actions taken during the audit are documented on the
audit form (single audit documentation).
There is the same LPA content for all audit levels.
Additional Comments/Observations:
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Step by Step- Ask corrective action and
follow up
The following must be fed into Fast Response on a weekly or shorter basis
Any High Risk finding
Any non-conformance that was not corrected at the time of the audit
Follow-Up
Additional Comments/Observations:
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Step by Step- Summarize audit finding
and track
Additional Comments/Observations:
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Key Learning Points-Take away
• LPA is a process to ensure compliance to procedure
for shop floor standards and standard work
• LPA process involves all levels of plant management
performing the same audit
• LPA results are measured for completion and
compliance
• LPA is an input to Fast Response, Fast Response
exit criteria include LPA
• Do it step by step
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Key Learning Points-Step by step
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