Roberto lopez LSSMBB [email protected] DMAIC project template.
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Transcript of Roberto lopez LSSMBB [email protected] DMAIC project template.
6 sigma steps (DMAIC)
• Define
• Measure
• Analyze
• Improve
• Control
• Define your business problem
• Measure your process (Y) performance
• Find the root causes (X’s) of the problem
• Improve, implement new solution
• Deliver Y performance over time
Description of the problem (what? where? since when? based on which data?Based on which facts?)
Voice Of Customer (Customer perception)Internal perception
Competitors benchmark
1 Pb Statement
Business Problem
Develop Goal statement/opportunity or objective in clear, concise, measurable termsDemonstrate alignment of the project with the company/business strategy
2 Goal Statement
Define
Why to do the project?
What if project not done?
Financial Business Case
Business Case
3 Business Case
What Comment Cost
K€
Project LaborProject MaterialsProject ContractorsEquipment investmentYearly operation costTOTAL Costs 0Incremental RevenuesLabor SavingsMaterial SavingsTOTAL Benefits (1 year) 0
ROI 0
Define
Green Belt/Black Belt role:Team members/role:
Black Belt:Master Black Belt:VP Quality / Quality Manager:
Manager:Key stakeholders from Business team:
Customers:Others:
4 Project scope
Project: in scope
D M A I CDates:Gantt
Project: out of scope
Project charter
5 Team
6
Planning
Define
7 (SIPOC)
Process map & CTQ’s
process as felt by the customer
Input Output
Supplier =My Company
Definition Specification Performance limit targets
CTQ*
Step 2Step 1 Step 3
measurement
*Critical To Quality
My Customer
Define
M-step 1:Selected CTQs
Selected Project CTQ(s):
Discrete/continuous CTQ?
CTQ Operational Definition(s):
What is it (measurement starting point and end point) ?
How to measure it?
What is a defect?
If applicable to your CTQ, LSL* contractual value or limit defined by customer:
If applicable to your CTQ USL* contractual value or limit defined by customer:
M-step 2:Define Performance standard
MeasureCTQ details
*LSL Lower Specification Limit*USL Upper Specification Limit
M-step 3: Measurement System Analysis
Measurement system analysis
Data Collection plan for Repeatability & Reproductibility study:Data sample size =Date of data collection:Where data have been collected?How data have been collected?How many operators? How many repeats per operator?
Gage R&R study – Continuous data:
-Tolerance (USL-LSL):
-Short method (yes/no):
-Gage R&R as %contribution: Gage R&R as %tolerance: Nb of distinct categories:
Gage R&R study – discrete data:If we have a Known sample (a reference), then how was built the known sample?
Conclusion/decision taken (evidence that the measurement of our CTQ is reliable):
MeasureGauge R&R
M-step 4: Baseline current (As Is) process capability
CTQ data collection plan•Data sample size =•Date of data collection:•Where data have been collected?•How data have been collected?
•Will you take the opportunity to collect obvious X’s when collecting your CTQ measurements?
•If yes, which X’s:
•Display an extract of the data collected:
MeasureCTQ data collection plan
Continuous CTQ•Sample size=•Short term data or Long term data?•Histogram with Normality test result and descriptive statistics:
•Type of the distribution (normal, other):•Trend represented by its (, median, Q1, Q3, other):
•Variability represented by its (P95, Q1/Q3, other):
PROCESS CAPABILITY MEASURE:NORMAL DistributionObserved DPMO=Potential DPMO=ZLT =ZST (ZLT+1.5)=
Conclusion•Problem with trend, variability or both?
M-step 4: Baseline current (As Is) process capability
Photography of current performanceMeasure
Non NORMAL DistributionObserved DPMO=Equivalent ZLT=Equivalent ZST (ZLT+1.5)=
Discrete CTQ•Sample size: •Short term data or Long term data?•Process capability
•Yield (%)=•%defects=•DPMO=•Opportunities per unit=•DPU=•Equivalent ZLT=
•Equivalent ZST (ZLT+1.5)=•95% confidence interval on DPMO:
MeasurePhotography of current performance
M-step 4: Baseline current (As Is) process capability
Continuous CTQ•Normal probability plot:
Conclusion (can we detect a true process and an unstable process?):
All type of CTQ•Stability over time/Run chart:
Conclusion:•Pb of technology (short term common causes)?•Pb of control (long term shift due to special causes)?•Both pbs?
A-step 5:As Is process Graph Analysis
AnalyzeGraph analysis
A-step 6: Define Performance Objectives of To Be process
Improvement GoalTarget (from benchmark) for:
Trend:Variability:LT DPMO or LT %defects=Yield (%)=ZLT=ZST=(ZLT+1.5)=
Gap (Improvement – Actual)DPMO gap or Defect reduction factor:Z gap=
6 Sigma tools necessary to meet performance objectives:• Ground fruit: Logic and Intuition• Low hanging fruit: Basic tools (Process Map, CE/CNX fishbone diagram, SOP, FMEA, Pareto, Histogram, Box plot)• Bulk of Fruit Process Characterization and Optimization• Sweet Fruit: Transform the project into a DFSS project
AnalyzeSet expected performance
A-step 7: Identify X’s (root causes)
Process (AS IS) detail analysis:•Detailed process map
Conclusion
•CTQ Intermediate distribution plot (continuous CTQ only)
Conclusion
Standard Operation Procedures analysis:•Exist:•Are applied:•Incitation to apply them exist:•Training has been given to operators:
Policy analysis:•Exist•Are applied
AnalyzeProcess analysis
List of potential significant X’s
Y/CTQ Output
Men
Machines
Materials
Methods
Measurements
Environment
Fishbone diagram of my Y
Label C/N/X on your fishbone, then rate every X impact vs implementation (table below)
1 2
3 4
Impact
High LowImplementation
Easy
Hard
AnalyzePotential root causes
A-step 7: Identify X’s (root causes)
Results of segmentation (continuous CTQ only) :(Box plots, Scatter plots, Distributions per X)
Conclusion:
AnalyzeSegmentation analysis
A-step 7: Identify X’s (root causes)
Pareto chart of the CTQ categories:
Conclusion:
Pareto chart of the defect categories:
Conclusion:
FMEA:
Conclusion:
AnalyzePareto analysis
A-step 7: Identify X’s (root causes)
Statistical Tests PerformedTest X Factors p value %contribution conclusion
one sample or two sample T-testAnnova one wayHomogeneity of varianceChi square testSimple regressionNon parametric data testANOVA 2 waysGLMDOE screening
Conclusion/Prioritized list of significant X’s:
Financial benefits confirmation (Update your Business case):
AnalyzeHypothesis testing
A-step 7: Identify X’s (root causes)
I-step 8:Screen potential causes.List improvement actions/projects
List of Vital few Xs (screening DOE): Improvement action plan (Who What When):
ImproveImprovement actions
I13
X tolerance settings:
I-step 9: Discover Variable relationships(if necessary)
Transfer function:
Proposed Solution: Optimal Settings
Confirmation runs capability:
I-step 10: Establish Operating Tolerances(if necessary)
ImproveImproved performance
ControlGage R&R on X’s
C-step 11:Define and Validate Measurement System on X’s(if necessary)
Control on one X (yes/no):
If yes, X measurement system analysis:
•Data Collection plan for Repeatability & Reproductibility study:Data sample size =Date of data collection:Where data have been collected?How data have been collected?How many operators? How many repeats per operator?
•Gage R&R study – Continuous data:
-Tolerance (USL-LSL):
-Short method (yes/no):
-Gage R&R as %contribution: Gage R&R as %tolerance: Nb of distinct categories:
•Gage R&R study – discrete data:If we have a Known sample (a reference), then how was built the known sample?
•Conclusion/decision taken (evidence that the measurement of our X is reliable):
C-step 12: Determine new Process Capability
Process or Product new capability:
Continuous CTQ:NORMAL DistributionObserved DPMO=Potential DPMO=ZLT =ZST (ZLT+1.5)=
Discrete CTQ:•Sample size:=•Short term data or Long term data?•Process capability•Yield (%)=•%defects=•DPMO=•Opportunities per unit=•DPU=•Equivalent ZLT=•Equivalent ZST (ZLT+1.5)=•95% confidence interval on DPMO
Statistical Confirmation of Improvement (by statistical test):
Confirmation of improved performanceControl
Non NORMAL DistributionObserved DPMO=Equivalent ZLT=Equivalent ZST (ZLT+1.5)=
C-step 13: Implement Process Control
Control Charts (SPC) in place/review mechanisms:
Mistake Proofing action taken:
FMEA control actions in place:
Process controlsControl