cqpr 2016 presentation

112
Business Excellence Consulting, Inc. Ph: 787.705.7272 – www.calidadpr.com Application of Six Sigma Tools in the Pharmaceutical Industry PRChem Annual Convention August 5th, 2016 Ritz Carlton Hotel and Casino, Isla Verde PR

Upload: duongnguyet

Post on 02-Jan-2017

214 views

Category:

Documents


0 download

TRANSCRIPT

Page 1: CQPR 2016 Presentation

Business Excellence Consulting, Inc.Ph: 787.705.7272 – www.calidadpr.com

Application of Six Sigma Tools in the Pharmaceutical Industry

PRChem Annual ConventionAugust 5th, 2016

Ritz Carlton Hotel and Casino, Isla Verde PR

Page 2: CQPR 2016 Presentation

Agenda

I. Six Sigma IntroductionII. Management and Organizational Infrastructure for Six SigmaIII. DMAIC Breakthrough MethodologyIV. Application of Tools: Define PhaseV. Application of Tools: Measure PhaseVI. Application of Tools: Analyze PhaseVII. Application of Tools: Improve PhaseVIII. Application of Tools: Control PhaseIX. Application of Tools for an Annual Product Review

2

Page 3: CQPR 2016 Presentation

This presentation is designed for those persons who are involved in implementing Six Sigma and want to understand its core concepts and benefits.

Provides an overview and orientation of Six Sigma methodologies and organizational requirements.

Audience

3

Page 4: CQPR 2016 Presentation

Course Objectives

ü Describe the Six Sigma Breakthrough strategyü Understand each participant’s role in the Six Sigma

Initiativeü Relate the roles and responsibilities of the

Champion, Black Belt, Green Belt and Team Members

ü Understand the DMAIC methodology and how it applies to improvement projects

4

Page 5: CQPR 2016 Presentation

Section I: Six Sigma Introduction

What is Six Sigma?

3-Sigma vs. 6-Sigma

Six Sigma Objective

What Makes Six Sigma Work?

DMAIC Roadmap

Page 6: CQPR 2016 Presentation

ü Management mandated and directed improvement program focused on breakthroughs in financial performance and customer satisfaction

ü Uses Champions, Black Belts and Green Belts to facilitate change

ü Focused on core business and Customer needs

ü A systematic method for process and product improvement

ü A Greek symbol for measuring performance variation

ü A metric for evaluating performance quality

ü A standard of excellence (3.4 defects per million opportunities)

What is Six Sigma?

6

Page 7: CQPR 2016 Presentation

3-Sigma vs. 6-Sigma

Page 8: CQPR 2016 Presentation

CenterProcess

ReduceSpread

Off-Target Too Much Variation

Centered On-Target

The objective is to understand customer requirements and reduce

process variation and defects

Six Sigma Objective

8

Page 9: CQPR 2016 Presentation

ü Select and work on the most important problems and projects to the business and Customer

ü Assure those projects impact customer satisfaction and financial performance

ü Allocate the time to get the work doneü Have your best people work on themü Provide those individuals with all the training, tools, and resources

they need to make the performance breakthroughü Provide Management direction, support and routine review of

performanceü Require a well thought out, objective and data driven solution ü Verify the dollar savings of your effortsü Sustain the benefits of the solution over time

What Makes Six Sigma Work?

9

Page 10: CQPR 2016 Presentation

Section II: Management Infrastructure for Six Sigma

Interrelationship of Six Sigma Infrastucture

Site Champion and Executive Staff

Hands on Champions

Master Black Belt

Black Belts / Green Belts

All Employees

Page 11: CQPR 2016 Presentation

Interrelationship of Six Sigma Infrastructure

Page 12: CQPR 2016 Presentation

Site Champion and Executive Staff

Functions

Set the vision

Create the mandate for improvement

Initiate and fund the activity

Establish and maintain the reporting structure

Responsibilities (10%+ of time)

Identify Champion/Sponsor in each functional area

Review of projects (members of Governance Boards)

Measure Project results

Training

2 day Champion Training12

Page 13: CQPR 2016 Presentation

Hands-On Champion (Sponsor)

Functions

Communicate the vision

Create the mandate for improvement

Provide direction and remove barriers

Achieve financial results and communicate success

Responsibilities (10%+ of time)

Identify Black Belts and Green Belts

Identify and approve all Six Sigma projects

Part of Governance Board

Measure Black Belt performance

Training

2 day Champion Training 13

Page 14: CQPR 2016 Presentation

Master Black Belt

Functions

Provide technical expertise on Six Sigma and Lean methodology to Black Belts and Green Belts

Work in support of the Black Belt and Champion

Assist in education and training activities

Responsibilities (100% of time)

Work daily with team members, Black Belts and Champions

Participate in the review of projects

Monitor all Six Sigma projects

Training

Black Belt Training, 2 years minimum as a Black Belt and a Masters Degree in a related field

14

Page 15: CQPR 2016 Presentation

Black Belts and Green Belts

FunctionsBlack Belts 100% dedicated to process improvement, Green Belts 20%Work on improvement projects with other Green Belts and Team MembersAchieve financial results for each project

Responsibilities (100 – 20%+ of time)Use the DMAIC methodology to create breakthroughs in performanceReport progress to the ChampionHold team meetings and provide project managementWork with the Master Black Belt

Training20 day Black Belt Training 10 day Green Belt Training

15

Page 16: CQPR 2016 Presentation

All Employees

Functions

Work to achieve excellence in daily work

Participate in Lean Six Sigma projects

Support team activities

Identify opportunities for improvement

Responsibilities (5-10%+ of time)

Participate in Lean Six Sigma activities as requested

Complete action items as assigned by the team

Attend team meetings

Training

1 day Lean Six Sigma Awareness training 16

Page 17: CQPR 2016 Presentation

Section III: DMAIC Breakthrough Methodology

Methodology

Process

Roadmap

Page 18: CQPR 2016 Presentation

DMAIC Methodology

18

Page 19: CQPR 2016 Presentation

DefineIdentify Project, Champion and Project OwnerDetermine Customer Requirements and CTQsDefine Problem, Objective, Goals and BenefitsDefine Stakeholder/Resource AnalysisMap the ProcessDevelop Project Plan

MeasureDetermine Critical Xs and YsDetermine Operational DefinitionsEstablish Performance StandardsDevelop Data Collection and Sampling PlanValidate the MeasurementsMeasurement Systems AnalysisDetermine Process Capability and Baseline

AnalyzeBenchmark the Process or ProductEstablish Causal Relationships Using DataAnalysis of the Process MapDetermine Root Cause(s) Using Data

ImproveDesign of ExperimentsDevelop Solution AlternativesAssess Risks and Benefits of Solution AlternativesValidate Solution using a PilotImplement SolutionDetermine Solution Effectiveness using Data

ControlStatistical Process ControlDetermine Needed Controls (measurement, design, etc.)Implement and Validate ControlsDevelop Transfer PlanRealize Benefits of Implementing SolutionClose Project and Communicate Results

DMAIC Roadmap

Page 20: CQPR 2016 Presentation

Section IV: Application of Tools -Define Phase

Project Charter

- Problem Statement

- Scope

- Goal Statement

- Resources

- Benefits

Project Charter Example

Page 21: CQPR 2016 Presentation

ü Problem

ü Objective & Scope

ü Goal/target

ü Resource requirements

ü Financial benefits

ü Strategic benefits

ü Team resources

ü Project approval

In this step you will establish direction for the project by documenting

Título del Projecto: Responsable: Espónsor del Projecto:

Caso de Negocios: (Resumen corto detallando los beneficios del proyecto, incluyendo la parte económica)

Escriba el caso de Negocios:

Descripción de la Oportunidad: (Detalle la oportunidad que el proyecto quiere mejorar)

Describa la Oportunidad:

Alcance del Projecto: (Defina los limites del proyecto)

Escriba los límites del Proyecto

Metas del Poyecto: Especifica Medible Alcanzable Relevante

Escriba las Metas del Proyecto

Miembros del Equipo (Listado de los miembros y sus funciones)

Listado de miembros del equipo aqui

Milestones/Deliverables: (Fecha que en que esperamos completar cada etapa)

D - M - A - M - C -

Project Charter

Page 22: CQPR 2016 Presentation

ü A description of the issue or problem

ü What, when, where and how the problem occurs

ü What is critical to quality (CTQ) from the customer perspective? What is nonconforming to specifications?

ü Define the boundaries of the problem, how big is the problem?

ü What are the consequences of the problem to the Company and or Customer?

ü Do not state a solution when describing a problem

Description of the “Pain”

Project Charter:Problem Statement

22

Page 23: CQPR 2016 Presentation

ü What process will the team focus on?

ü What are the boundaries of the process we are to improve? Where does the process begin? Where does it end?

ü Which customers will be affected / included

ü What is outside of scope for the team?

ü What constraints or timelines must the team work under?

Customer or Suppliers Site or Line Process

Process 1

Process 2

Process 3

Project Charter:Scope

Page 24: CQPR 2016 Presentation

Goal Statement Example:

Reduce Packaging Line #2 scrap by 33% at the end of 3Q 2016.

ü Describe, in measurable terms, what success will look like when you’ve solved the problem

ü Include a statement of the performance level that will satisfy your CTQ and the time frame in which you plan to implement the improvement. State targets and tolerances where appropriate.

Project Charter:Goal Statement

24

Page 25: CQPR 2016 Presentation

Determine the Stakeholders

Who will need to be involved and at what level for this project to be successful?

Determine Team Members

Who will need to be on the team and at what % of their time?

Determine any Capital or HR Requirements

What materials, testing, software programming, outside services or equipment will be needed? Are those costs acceptable to management?

Other Support to be Successful

Project Charter:Resources

25

Page 26: CQPR 2016 Presentation

ü Benefits may include any of the following:ü Hard dollar savings (cost reduction)ü Soft dollar savings (cost avoidance)ü Improved Customer satisfactionü Improvement in the performance metrics (cycle time, yield,

defects, etc.) ü Improved job satisfaction (reduction in frustration)ü When considering benefits… what must change for the

savings to occur?

Project Charter:Benefits

26

Page 27: CQPR 2016 Presentation

27

Page 28: CQPR 2016 Presentation

Section V: Application of Tools -Measure Phase

Measurement System Analysis

Process Capability

Graphical Tools:

- Histogram / Dotplot

- Boxplot

- Pareto- Scatterplot

Page 29: CQPR 2016 Presentation

Measurement System Analysis

29

Page 30: CQPR 2016 Presentation

30

Elements of Variation

Page 31: CQPR 2016 Presentation

◆ Each operator measures the same part several times.◆ Data must be balanced; that is, operators must measure

each part the same number of times.◆ Units must represent the whole range of expected

variation. It is recommended to select parts within the specification range, that is, parts from the lower specification limit, parts from the upper specification limit, and parts within the specification limits.

◆ Operators must measure the parts randomly. They must not know which part number they are measuring at any given time.

31

Gage R&R Basics

Page 32: CQPR 2016 Presentation

32

Gage R&R Metrics

◆ Repeatability—The variation caused by the instrument. It is the variation observed when an operator measures the same part repeatedly using the same measurement instrument.

◆ Reproducibility—The variation caused by the measurement system. It is the variation observed when several operators measure the same part using the same instrument.

◆ Percent precision-to-tolerance (% P/T)—The percentage of the specification tolerance occupied by the measurement system variation.

◆ Percent gage R&R (% R&R)—The percentage of the total variation occupied by the measurement system.

Page 33: CQPR 2016 Presentation

33

Performing a Gage R&R

Page 34: CQPR 2016 Presentation

34

Performing a Gage R&R

Page 35: CQPR 2016 Presentation

Process Capability

35

Page 36: CQPR 2016 Presentation

Analyzing Process Capability

Capable Process

Incapable Process 36

Page 37: CQPR 2016 Presentation

Process Capability Indices

37

Page 38: CQPR 2016 Presentation

Interpreting the Process Capability Indices

38

Page 39: CQPR 2016 Presentation

Process Capability Example

39

Page 40: CQPR 2016 Presentation

Process Capability Example cont.

40

Individuals

Moving Range

Page 41: CQPR 2016 Presentation

Process Capability Example cont.

41

Page 42: CQPR 2016 Presentation

Process Capability Example cont.

42

Page 43: CQPR 2016 Presentation

Process Capability Example cont.

43

Page 44: CQPR 2016 Presentation

Graphical Tools

44

Page 45: CQPR 2016 Presentation

Describing the Data:Histograms

45

Page 46: CQPR 2016 Presentation

Describing the Data:Dotplots

46

Page 47: CQPR 2016 Presentation

Comparing Groups:Boxplots

47

Page 48: CQPR 2016 Presentation

Prioritizing Our Actions:The Pareto Diagram

48

Page 49: CQPR 2016 Presentation

Analyzing Relationships:The Scatterplot

49

Page 50: CQPR 2016 Presentation

Section VI: Application of Tools -Analyze Phase

Hypothesis Tests:

- 1 sample t, 2 sample t, ANOVA

- 1 sample sign, Krustal-Wallis

- F test, Levene

Page 51: CQPR 2016 Presentation

◆ A hypothesis test is a method of making decisions using data from our processes.

◆ In statistics, a result is called statistically significant if it is unlikely to have occurred by common causes of variation alone, according to a predetermined threshold probability called the significance level.

51

Overview

Page 52: CQPR 2016 Presentation

◆ If the p-value is less than the required significance level, then we say the null hypothesis is rejected at the given level of significance. – Under this scenario, we might accept the alternate

hypothesis. ◆ If the p-value is not less than the required significance

level, then the test has no result. – The evidence is insufficient to support a conclusion.

52

Overview

Page 53: CQPR 2016 Presentation

◆ To summarize, here is a slogan you can use to remember when to reject or fail to reject the null hypothesis (H0):

“If p-value is low, the null hypothesis must go.”

◆ In other words, when the p-value for the null hypothesis is lower than a predetermined value, then the null hypothesis must be rejected.

53

Overview

Page 54: CQPR 2016 Presentation

◆ When dealing with hypothesis testing, there are four decisions that can be made.

◆ Two of those decisions are correct decisions, while two of them are wrong decisions.

◆ In statistics, those wrong decisions are called type I error and type II error.

54

Overview

Page 55: CQPR 2016 Presentation

55

Overview

Page 56: CQPR 2016 Presentation

◆ One-Sample t-Test– Comparing one average to a target value

◆ Two-Sample t-Test– Comparing the averages of two populations

◆ One-Way ANOVA Test– Comparing the averages of two or more populations, using

just one factor

56

Comparing Means

Page 57: CQPR 2016 Presentation

Three months ago, a company implemented a new CAPA investigation process after a massive training. The company wants to know if the training is paying off, that is, if the average closure time for the investigations has decreased significantly. Before training, average closure time was 20 days.

57

One-Sample t-Test Example

Page 58: CQPR 2016 Presentation

58

One-Sample t-Test Example

Page 59: CQPR 2016 Presentation

A company wants to compare how long it takes (in hours) for each shift in the quality control laboratory to perform an analytical test on a specific product. There are two shifts: shift 1 and shift 2. A given test is selected, and the times to complete that test are collected and analyzed with statistical software.

59

Two-Sample t-Test Example

Page 60: CQPR 2016 Presentation

Two-Sample t-Test Example

NOTE: A test for variances must be performed prior to the two-sample t-test

Page 61: CQPR 2016 Presentation

61

Two-Sample t-Test Example

Page 62: CQPR 2016 Presentation

A company wants to compare the performance of three shifts in terms of the manufacturing cycle time to determine if there are significant differences in their averages. After verifying the assumptions related to normality of the data and equal variances, the box plots shown in the next page were developed and a One-Way ANOVA performed.

62

One-Way ANOVA Example

Page 63: CQPR 2016 Presentation

63

One-Way ANOVA Example

Page 64: CQPR 2016 Presentation

64

One-Way ANOVA Example

Page 65: CQPR 2016 Presentation

Although it was proven that the average manufacturing cycle time for each shift was not statistically different, the performance among the shifts does not appear to be the same. For that reason, the company developed a quality index to measure their performance. The index is based on a scale of 1 to 5, where 1 means poor performance and 5 means excellent performance.

65

One-Way ANOVA Example

Page 66: CQPR 2016 Presentation

66

One-Way ANOVA Example

Page 67: CQPR 2016 Presentation

67

One-Way ANOVA Example

Page 68: CQPR 2016 Presentation

◆ One-Sample Sign Test– Comparing one median to a target value– Non-parametric equivalent to the one-sample t-test

◆ Two-Sample Mann-Whitney Test– Comparing the medians of two populations– Non-parametric equivalent to the two-sample t-test

◆ Krustal-Wallis Test– Comparing the medians of two or more populations, using

just one factor– Non-parametric equivalent to the ANOVA test

68

Comparing Medians

Page 69: CQPR 2016 Presentation

The median cycle time for investigation has been 25 days (50% of investigations needed more than 25 days to be completed). After new root cause analysis training, three months of data were used to evaluate the improvement (if any).

69

One-Sample Sign Test Example

Page 70: CQPR 2016 Presentation

70

One-Sample Sign Test Example

Page 71: CQPR 2016 Presentation

A pharmaceutical company wanted to determine if there are significant differences in the hardness of the tablet they manufacture using two different pieces of equipment. In order to analyze this, a period of one year of production was collected from each machine. After performing a normality test, it was noticed that data do not follow the normal distribution. The histograms in the next page show a p-value for the Anderson-Darling normality test of 0.0000 for each machine, indicating that the data do not follow the normal distribution.

71

Two-Sample Mann-Whitney Test Example

Page 72: CQPR 2016 Presentation

72

Two-Sample Mann-Whitney Test Example

Page 73: CQPR 2016 Presentation

73

Two-Sample Mann-Whitney Test Example

Page 74: CQPR 2016 Presentation

A pharmaceutical company wanted to analyze three different suppliers of a fluid used in their manufacturing process in order to select one of them. A critical characteristic of the fluid is viscosity, measured in centipoise (cP). The specifications for the viscosity of the fluid range from 2.4 to 3.6 cP. Data from the three suppliers were analyzed and a histogram and descriptive statistics of them generated.

74

Krustal-Wallis Test Example

Page 75: CQPR 2016 Presentation

75

Krustal-Wallis Test Example

Page 76: CQPR 2016 Presentation

76

Krustal-Wallis Test Example

Page 77: CQPR 2016 Presentation

◆ F-test– Comparing variances of two populations

◆ Bartlett Test– Comparing variances of two or more populations

◆ Levene Test– Comparing variances of two or more populations when

they do not fit a Normal distribution

77

Comparing Variances

Page 78: CQPR 2016 Presentation

A company wants to analyze two different adhesives for the transdermal patches they manufacture. Adhesives on a patch generally help maintain contact between the transdermal system and skin surface. The adhesiveness of the patches is critical in the drug delivery mechanism, its safety, product quality, and efficacy. As such, a good adhesive should easily adhere to the skin with an applied finger pressure and be tacky enough to maintain a strong holding force. The adhesive should also be easily removed from the skin without leaving a residue. The specification for the adhesiveness of the transdermal patch ranges from 300 to 3500 g/system.

78

F-test

Page 79: CQPR 2016 Presentation

79

F-test

Page 80: CQPR 2016 Presentation

80

F-test

Page 81: CQPR 2016 Presentation

Let us suppose that in the previous example the manufacturer would like to test a third adhesive. Since the F-test can only compare two variances at a time, we need to perform a Bartlett test.

81

Bartlett Test Example

Page 82: CQPR 2016 Presentation

82

Bartlett Test Example

Page 83: CQPR 2016 Presentation

83

Bartlett Test Example

Page 84: CQPR 2016 Presentation

84

Bartlett Test Example

Page 85: CQPR 2016 Presentation

A pharmaceutical company wants to evaluate the time it takes their analysts to perform a certain laboratory test. They have noticed too much variation in the time it takes the various shifts to complete the test and would like to investigate the reason for the variation. In order to start the analysis, the time it took each analyst to perform the laboratory test (in hours) is collected. Then, the data are segregated by shift.

85

Levene Test Example

Page 86: CQPR 2016 Presentation

86

Levene Test Example

Page 87: CQPR 2016 Presentation

87

Levene Test Example

Page 88: CQPR 2016 Presentation

88

Most Commonly Used Hypothesis Tests

Page 89: CQPR 2016 Presentation

Section VII: Application of Tools -Improve Phase

Lean Tools

Control Charts

Page 90: CQPR 2016 Presentation

◆ Value stream mapping◆ Minimization of non-value added activities◆ Set-up reduction (SUR)◆ The use of standard operating procedures◆ Total productive maintenance◆ Poka-yoke techniques to prevent or detect errors ◆ Workplace organization (5S approach)◆ Just-in-time principles◆ Continuous flow manufacturing concepts 90

Lean Techniques

Page 91: CQPR 2016 Presentation

Control Charts

91

Page 92: CQPR 2016 Presentation

Section VIII: Application of Tools -Control Phase

Rational Subgroups

Nonrandom Patterns

Variables Control Charts:

- IMR, Xbar & R, Xbar & s

Attributes Control Charts:- p, np, c, u

Page 93: CQPR 2016 Presentation

◆ One of the most important concepts in control charting is the rational subgroup.

◆ A rational subgroup is just a subset of a group intended to be as homogeneous as possible. In that way, we will be able to compare the variation within each subgroup and compare the variation between subgroups over an extended period.

◆ But how do we determine the appropriate subgroup size? That will depend on the process being studied. 93

The Rational Subgroup

Page 94: CQPR 2016 Presentation

94

Nonrandom Patterns

Page 95: CQPR 2016 Presentation

◆ Test 1—One point more than 3 sigma from centerline◆ Test 2—Nine points in a row on same side of centerline◆ Test 3—Six points in a row, all increasing or all decreasing◆ Test 4—Fourteen points in a row, alternating up and down◆ Test 5—Two out of three points in a row more than 2 sigma from

the centerline (same side)◆ Test 6—Four out of five points in a row more than 1 sigma from the

centerline (same side)◆ Test 7—Fifteen points in a row within 1 sigma from the centerline

(either side)◆ Test 8—Eight points in a row more than 1 sigma from the centerline

(either side)95

Nonrandom Patterns

Page 96: CQPR 2016 Presentation

◆ Individuals and Moving Range Chart» Subgroup size = 1

◆ X-bar and R Chart» Subgroup size from 2 to 5

◆ X-bar and s Chart» Subgroup greater than 5

96

Variables Control Charts

Page 97: CQPR 2016 Presentation

97

Variables Control ChartsA

vera

geR

ange

Page 98: CQPR 2016 Presentation

◆ p Chart: percent defectives◆ np chart: number of defectives◆ c chart: number of defects◆ u chart: avg. number of defects per unit

98

Attributes Control Charts

Page 99: CQPR 2016 Presentation

99

Attributes Control Charts

Page 100: CQPR 2016 Presentation

100

Attributes Control Charts

Page 101: CQPR 2016 Presentation

101

Attributes Control Charts

Example of p Chart

Page 102: CQPR 2016 Presentation

Section IX: Application of Tools for an Annual Product Review

Descriptive Statistics

Process Capability

Hypothesis Tests

Page 103: CQPR 2016 Presentation

103

Process Monitoring for an Annual Product Review (APR)

Page 104: CQPR 2016 Presentation

104

Process Monitoring for an Annual Product Review (APR)

Page 105: CQPR 2016 Presentation

105

Process Monitoring for an Annual Product Review (APR)

Page 106: CQPR 2016 Presentation

106

Process Monitoring for an Annual Product Review (APR)

Page 107: CQPR 2016 Presentation

107

Process Monitoring for an Annual Product Review (APR)

Page 108: CQPR 2016 Presentation

108

Process Monitoring for an Annual Product Review (APR)

Page 109: CQPR 2016 Presentation

Thanks !!!

109

Page 110: CQPR 2016 Presentation

Business Excellence Consulting Inc.

110

Page 111: CQPR 2016 Presentation

Business Excellence Consulting Inc.

111

Page 112: CQPR 2016 Presentation

Business Excellence Consulting Inc.

112

www.calidadpr.com