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Process System CapabilityProcess System CapabilityAn introduction to 9103An introduction to 9103
‘‘VARIATION MANAGEMENT OF VARIATION MANAGEMENT OF KEY CHARACTERISTICS’KEY CHARACTERISTICS’
Bernard LAURAS
AIRBUS
Objectives of this Objectives of this presentationpresentation
• Show importance of managing Key Characteristics Show importance of managing Key Characteristics and Increase your understanding of 9103 content. and Increase your understanding of 9103 content.
• Share experiences of implementing 9103 including Share experiences of implementing 9103 including who was involved and what they got out of it.who was involved and what they got out of it.
• Inspire you that 9103 has broader benefits and is Inspire you that 9103 has broader benefits and is not just a Customer requirement.not just a Customer requirement.
• Illustrate that small organisations can do this type of Illustrate that small organisations can do this type of activity.activity.
• 9103 should help resolve the first 4 main causes of 9103 should help resolve the first 4 main causes of
Quality problems identified by AIA (Aerospace Quality problems identified by AIA (Aerospace
Industry Association)Industry Association)
– Personnel fail to understand the design requirementPersonnel fail to understand the design requirement
– Process changed without understanding the impactProcess changed without understanding the impact
– Process to review initial production fails to detect defectsProcess to review initial production fails to detect defects
– Design requirements exceed the capability of the Design requirements exceed the capability of the
manufacturing processmanufacturing process
Why do we need such Why do we need such presentation ?presentation ?
9103 exists, so why the problems ?
9103 exists, so why the problems ?
Why do we need such Why do we need such presentation ?presentation ?
• 9103 not sufficiently and adequately 9103 not sufficiently and adequately deployeddeployed
Value not clearly identified Value not clearly identified or understoodor understood All functions to be involved, All functions to be involved, not only Qualitynot only Quality
Training requiredTraining required Need to explain how to Need to explain how to apply 9103 based upon apply 9103 based upon supplier & product complexitysupplier & product complexity
Lack of skillsLack of skills
Lack of buy-inLack of buy-in
What are Key Characteristics ?What are Key Characteristics ?
Key Characteristics are the main ones guaranteeing Key Characteristics are the main ones guaranteeing full Customer satisfaction, that means ensuring all his full Customer satisfaction, that means ensuring all his
needs are effectively & permanently metneeds are effectively & permanently met
Why do we need to focus on Why do we need to focus on key characteristics ?key characteristics ?
• To enhance confidence that true Customer To enhance confidence that true Customer expectations are metexpectations are met
• To drive the continuous improvement of To drive the continuous improvement of manufacturing processes through adequate manufacturing processes through adequate planningplanning
• To reduce costs by eliminating wastes and To reduce costs by eliminating wastes and unnecessary effortsunnecessary efforts
Scope of 9103Scope of 9103
• Primarily intended to Primarily intended to apply to new partsapply to new parts but but should should also be applied through out the life of also be applied through out the life of the programmethe programme to ensure that to ensure that changes are changes are taken into consideration.taken into consideration.
• Establishes requirements for management of Establishes requirements for management of key characteristics variation key characteristics variation
– Specifies Specifies general requirementsgeneral requirements
– Provides a Provides a processprocess
Process for Key Characteristic Process for Key Characteristic Variation Management : 7 stepsVariation Management : 7 steps
Understand key characteristics and
required performance
Plan a process that will produce acceptable
performance
Operate the process to generate data
Continue to monitor the performance
Analyse data to identify appropriate
action
Take action from study (operate, redesign and
improve)
Is a process change
required?
Yes No
Stage 1Stage 1
Understand key characteristics and
required performance
Plan a process that will produce acceptable
performance
Operate the process to generate data
Continue to monitor the performance
Analyse data to identify appropriate
action
Take action from study (operate, redesign and
improve)
Is a process change
required?
Yes No
Understand key characteristics and
required performance
Stage 1 - Understand Key Stage 1 - Understand Key Characteristics and Required Characteristics and Required PerformancePerformance
• Establish an appropriateEstablish an appropriatecross-functional teamcross-functional team
– Design Engineer:Design Engineer: Potential design failure Potential design failure modes, modes, causes and effects.causes and effects.
– Manufacturing Engineer: Manufacturing Engineer: Process issues, potential Process issues, potential failures, failures, causes and effects.causes and effects.
– Inspection Department:Inspection Department: Definition of inspection methods and Definition of inspection methods and criteria.criteria.
– Buyer (Purchasing):Buyer (Purchasing): Feedback from Supply Chain and Feedback from Supply Chain and flow down of requirements.flow down of requirements.
– Quality Engineer (Facilitator):Quality Engineer (Facilitator): Feedback from similar product, Feedback from similar product, customer returns, guarantee customer returns, guarantee
that that process is adequately process is adequately followed.followed.
Adapt it to your C
ompany…
Adapt it to your C
ompany…
and don’t forget th
e Operators
and don’t forget th
e Operators
who effectively do the job !
who effectively do the job !
Stage 1 - Understand Key Stage 1 - Understand Key Characteristics and Required Characteristics and Required PerformancePerformance
• Establish an appropriateEstablish an appropriatecross-functional teamcross-functional team
– Design Engineer:Design Engineer: Potential design failure Potential design failure modes, modes, causes and effects.causes and effects.
– Manufacturing Engineer: Manufacturing Engineer: Process issues, potential Process issues, potential failures, failures, causes and effects.causes and effects.
– Inspection Department:Inspection Department: Definition of inspection methods and Definition of inspection methods and criteria.criteria.
– Buyer (Purchasing):Buyer (Purchasing): Feedback from Supply Chain and Feedback from Supply Chain and flow down of requirements.flow down of requirements.
– Quality Engineer (Facilitator):Quality Engineer (Facilitator): Feedback from similar product, Feedback from similar product, customer returns, guarantee customer returns, guarantee
that that process is adequately process is adequately followed.followed.
• Look at product, process & Customer requirements: Look at product, process & Customer requirements: What What does he want and how we can do it ?does he want and how we can do it ?
Listen to
your C
ustomer
Listen to
your C
ustomer
Speak with
your C
ustomer
Speak with
your C
ustomer
Stage 2Stage 2
Understand key characteristics and
required performance
Plan a process that will produce acceptable
performance
Operate the process to generate data
Continue to monitor the performance
Analyse data to identify appropriate
action
Take action from study (operate, redesign and
improve)
Is a process change
required?
Yes NoPlan a process that will
produce acceptable performance
Stage 2 - Plan Manufacturing Stage 2 - Plan Manufacturing ProcessesProcesses
• Ensure process owner exist for Ensure process owner exist for each key characteristiceach key characteristic
• Establish a minimum acceptable Establish a minimum acceptable capability ratio (Ck, Cpk, …) for capability ratio (Ck, Cpk, …) for each key characteristiceach key characteristic
• Identify sources of variation and Identify sources of variation and potential risks… and mitigate thempotential risks… and mitigate them
• Relate process data back to what Relate process data back to what designers want…designers want…
• Identify key manufacturing processes Identify key manufacturing processes impacting key characteristicsimpacting key characteristics
• … … and designers: Also understand and designers: Also understand capability of manufacturing Processescapability of manufacturing Processes
Stage 3Stage 3
Understand key characteristics and
required performance
Plan a process that will produce acceptable
performance
Operate the process to generate data
Continue to monitor the performance
Analyse data to identify appropriate
action
Take action from study (operate, redesign and
improve)
Is a process change
required?
Yes NoOperate the process to generate data
Stage 3 - Operate on Trial Stage 3 - Operate on Trial Basis to Generate DataBasis to Generate Data
Date (Rev)
STAGE 5
Hist / New Date Gauge Gauge # MSA % n Freq. Mean Cp Cpk Type Frequency
1 New 14/ 03/ 2001 CMM 86373 11.4 20 100% xmR Yes 0.326 1.15 1.47 Yes Comp 10% Quarterly
2 Hist 14/ 03/ 2001 Micr 10265 15.8 500 20% xmR Yes 0.05 1.98 1.54 No Manual 20% Quarterly
PROCESS CONTROL DOCUMENT Page 2 of 2
Capability Review Freq.
Ongoing Monitoring Methods
Control Chart/Other
STAGE 3 STAGE 4 STAGE 6
Results of Study
StableY / N
Calculations
Process Control Document Number
Action from Study,
Y/N
0.0015
Part Number / Latest Change Level Date (Original)
Estimated St Dev
CCF No.
Preliminary Process Capability Study -Type of Control Chart
0.034
ABC123
ABC123
FK5678, Rev 2.0 28/ 08/ 0114/ 03/ 01
Date (Original) Date (Rev) Flowchart Created? Yes/No
Cp Cpk
1 L/ E fi lm cooling hole position EDM H006 Rev. 4 01/ 02/ 01 1.33 1.33 Manuf acturer defined Yes Yes
Conformance Control Feature Are Sources of Variation Identified?
Yes/No
Is Risks Mitigation Specified?
Yes/No
Minimum Requirement
Origin of CCF
Process Owner
Producer Approvals and Date
Name:
CCF No
Manufacturer Code Name:
Process ID OperationNumber
Work Instruction No. /Change Level
CCF Name
PROCESS CONTROL DOCUMENT Page 1 of 2
STAGE 1
Part Name / Description
Producer / Plant
Process Control Document Number
Name:
STAGE 2
Customer Approvals and Date
Name:
ABC123 14/ 03/ 01
High Pressure Turbine Blade, Trent 900, FK5678
Rolls-Royce HPTB Facility,Derby TBF12
Michael Edwards 28/ 08/ 01
M Engineer 25/ 08/ 01
C Owner 26/ 08/ 01
T Rent 27/ 08/ 01
• Create Data collection plan for Create Data collection plan for all key characteristics (who, what, all key characteristics (who, what, where, frequency, conditions,…)where, frequency, conditions,…)
•Produce parts/components to Produce parts/components to specified work instructions in specified work instructions in a representative environmenta representative environment
•Measure key characteristics and collect Measure key characteristics and collect data to document any deviationsdata to document any deviations
• Perform First Article Inspection (9102 Perform First Article Inspection (9102 Refers).Refers).
Stages 4 and 5Stages 4 and 5
Understand key characteristics and
required performance
Plan a process that will produce acceptable
performance
Operate the process to generate data
Continue to monitor the performance
Analyse data to identify appropriate
action
Take action from study (operate, redesign and
improve)
Is a process change
required?
Yes No
Analyse data to identify appropriate action
Take action from study (operate, redesign and
improve)
Stages 4 & 5 - Analyse Data and Stages 4 & 5 - Analyse Data and launch appropriate Actionlaunch appropriate Action
• Process not stable : Perform Process not stable : Perform root cause analysis with root cause analysis with proper tools and document it.proper tools and document it.
Review control charts to determine if process is stableReview control charts to determine if process is stable
• When process is stable, calculate process capability and When process is stable, calculate process capability and compare with what is required to meet Customer needscompare with what is required to meet Customer needs
• Remove or minimise causes… Remove or minimise causes… and verify effectiveness of and verify effectiveness of corrective actionscorrective actions
•88
•90
•92
•94
•96
•98
•100
•1 •2 •3 •4 •5 •6 •7 •8 •9 •10 •11 •12
ActualLCL (Lower Control Limit)
UCL
LCL
UCL (Upper Control Limit)
Stages 4 & 5 - Analyse Data and Stages 4 & 5 - Analyse Data and launch appropriate Action launch appropriate Action (Continued)(Continued)
• Launch a new root cause Launch a new root cause analysis analysis •Prioritise causes of variation Prioritise causes of variation and identify most influential onesand identify most influential ones• Investigate centering of the Investigate centering of the processprocess
If process stable but not capableIf process stable but not capable
LSL(Lower Spec Limit)
USL(Upper Spec Limit)
LSL(Lower Spec Limit)
USL(Upper Spec Limit)
•••90
•••92
•••94
•••96
•••98
•••100
•••102
•••104
•••1 •••2 •••3 •••4 •••5 •••6 •••7 •••8 •••9 •••10 •••11 •••12•••90
•••92
•••94
•••96
•••98
•••100
•••102
•••104
•••1 •••2 •••3 •••4 •••5 •••6 •••7 •••8 •••9 •••10 •••11 •••12
LCL (Lower Control Limit)
UCL (Upper Control Limit)
Stages 4 & 5 - Analyse Data and Stages 4 & 5 - Analyse Data and launch appropriate Action launch appropriate Action (Continued)(Continued)
• Prioritise causes of variationPrioritise causes of variation• Identify most influential root Identify most influential root causescauses• Investigate centering of the Investigate centering of the processprocess
If process stable but not capableIf process stable but not capable
LSL(Lower Spec Limit)
USL(Upper Spec Limit)
LSL(Lower Spec Limit)
USL(Upper Spec Limit)
•••90
•••92
•••94
•••96
•••98
•••100
•••102
•••104
•••1 •••2 •••3 •••4 •••5 •••6 •••7 •••8 •••9 •••10 •••11 •••12•••90
•••92
•••94
•••96
•••98
•••100
•••102
•••104
•••1 •••2 •••3 •••4 •••5 •••6 •••7 •••8 •••9 •••10 •••11 •••12
LCL (Lower Control Limit)
UCL (Upper Control Limit)
When actions are taken that change the
When actions are taken that change the
manufacturing processes, repeat th
e
manufacturing processes, repeat th
e
process starting at Stage 2 (P
lan
process starting at Stage 2 (P
lan
Manufacturing Process).
Manufacturing Process).
Stage 6Stage 6
Understand key characteristics and
required performance
Plan a process that will produce acceptable
performance
Operate the process to generate data
Continue to monitor the performance
Analyse data to identify appropriate
action
Take action from study (operate, redesign and
improve)
Is a process change
required?
Yes NoContinue to monitor the Performance
Stage 6 - Continue to Monitor the Stage 6 - Continue to Monitor the PerformancePerformance
When characteristics are meeting Customer’s requirements, When characteristics are meeting Customer’s requirements, continue to measure periodically to detect possible long term continue to measure periodically to detect possible long term variations and identify opportunities for improvement.variations and identify opportunities for improvement.
Process Capability
UpperProcess
Limit
LowerProcessLimit
THE VOICE OF THE PROCESS
UpperSpecification
Limit
Drawing Tolerance
LowerSpecificationLimit
THE VOICE OF THE CUSTOMERTHE VOICE OF THE CUSTOMER
What w
e
do want
Stage 6 - Continue to Monitor Stage 6 - Continue to Monitor PerformancePerformance
UpperSpecification
Limit
LowerSpecificationLimit
THE VOICE OF THE CUSTOMERTHE VOICE OF THE CUSTOMER
Process CapabilityTHE VOICE OF THE PROCESS
UpperProcess
Limit
LowerProcessLimit
Drawing Tolerance
What w
e do
not want
UpperSpecification
Limit
LowerSpecificationLimit
THE VOICE OF THE CUSTOMERTHE VOICE OF THE CUSTOMER
Process CapabilityTHE VOICE OF THE PROCESS
UpperProcess
Limit
LowerProcessLimit
Drawing Tolerance
What w
e do
not want
When characteristics are meeting Customer’s requirements, When characteristics are meeting Customer’s requirements, continue to measure periodically to detect possible long term continue to measure periodically to detect possible long term variations and identify opportunities for improvement.variations and identify opportunities for improvement.
Stage 7Stage 7
Understand key characteristics and
required performance
Plan a process that will produce acceptable
performance
Operate the process to generate data
Continue to monitor the performance
Analyse data to identify appropriate
action
Take action from study (operate, redesign and
improve)
Is a process change
required?
Yes No
Is a process change
required?
Stage 7 – Is a process change Stage 7 – Is a process change required ?required ?
• If no change is required, continue to If no change is required, continue to monitor process performance per Stage 6.monitor process performance per Stage 6.
• If a change is required, repeat Stages 1 to If a change is required, repeat Stages 1 to 5 prior to implementing any change.5 prior to implementing any change.
• Document any planned manufacturing Document any planned manufacturing process changes, including reasons for process changes, including reasons for change.change.
On target with On target with minimum variationminimum variation
Plan
DoControl
Act
Continuous Continuous ImprovementImprovement
9103 successful Management…
… A never ending process
Summary : Don’t forget these Summary : Don’t forget these key factors of success…key factors of success…• Manage Keys characteristics during all life of the Manage Keys characteristics during all life of the
programme, in particular when introducing a changeprogramme, in particular when introducing a change• Involve all concerned functionsInvolve all concerned functions• Focus on key characteristics and associated Focus on key characteristics and associated
processes… but don’t forget the others !processes… but don’t forget the others !• Record all what you do… and keep historyRecord all what you do… and keep history ::
– Potential loss of experience during the programme lifePotential loss of experience during the programme life– Change of rationale for a characteristics being key or notChange of rationale for a characteristics being key or not
• Feedback from manufacturing & supply chain to Feedback from manufacturing & supply chain to engineeringengineering
… … and flow them down internally and and flow them down internally and within your Sub-Tierswithin your Sub-Tiers
Next StepNext Step
• Training module, guidance material, on line Training module, guidance material, on line training packs, etc …will be created by IAQG training packs, etc …will be created by IAQG
0 10 20
120
170
220
270Individual and MR Chart
Obser.
Indi
vidu
al V
alue
1
Mean=200.2
UCL=253.3
LCL=147.0
0
30
60
90
Mov
.Ran
ge
1
1
R=20
UCL=65.35
LCL=0
0 10 20
Last 20 Observations
150
175
200
225
Observation Number
Val
ues
130 270
Capability PlotProcess Tolerance
I I I
I I I
I ISpecifications
Within
Overall
140 190 240
Normal Prob Plot
130 180 230
Capability Histogram
WithinStDev:Cp:Cpk:
17.73051.321.31
OverallStDev:Pp:Ppk:
19.33771.211.20
Output from Minitab Software
Any Questions ?Any Questions ?
They will be answered at the endThey will be answered at the end
of the 3 presentationsof the 3 presentations
Existing experience of 9103 Existing experience of 9103 ImplementationImplementation
Brian HarveyBrian Harvey - Clamonta - Clamonta
Dave Wentworth - Delta Industries Dave Wentworth - Delta Industries