Professional Documents
Culture Documents
1 Quality Management
What do you mean by “Interchangeable Parts”? Any Organisation
associated with the same?
2 Quality Management
What is the process of implementing TQM in above
cases?
What is SPC?
4 Quality Management
EVOLUTION OF QUALITY
TIME DEVELOPMENTS
Prior to 20th Quality is an Art. An era of workmanship
Century
1800s Interchangeable Parts
1924 Walter Shewhart :Statistical Approach to Quality/
Control Charts
1950 Visit of Deming in Japan at the invitation of
K.Ishikawa
1954 TQC in Japan ( Visit of Juran to Japan)
A.V.Feigenbaum conceptualized TQC / Systems Approach
to quality
1961 The Martin (Marietta) Co. in USA introduces the zero-
defects ‘approach’ while developing and producing
Missiles (Philip Crosby’s Approach to Quality).
5 Quality Management
EVOLUTION OF QUALITY
TIME DEVELOPMENTS
1962-70 The concept of Total Quality is affirmed and devised in Japanese
industries./Quality circle introduced in Japan ( By K. Ishikawa)
6 Quality Management
WALTER A SHEWHART
40,000 people, out of which 5,200 people were in the
Inspection Department (Western Electric, Hawthorne
Works)
In 1924 he proposed the Control Chart as a method to
determine when a process was in a state of Statistical
control
Economic Control of Quality of Manufactured Product,
published in 1931, is regarded as a complete and
thorough exposition of the basic principles of quality
control
Visited India in 1947-48 under the sponsorship of P. C.
Mahalanobis
Shewhart is referred to as the “father of statistical quality
control
7 Quality Management
PHASES OF QUALITY
9 Quality Management
PHASES OF QUALITY
Total Quality Management:
Management approach of an Organization ,centered on
quality, based on the participation of all its members and
aiming at long term Success through customer
satisfaction and benefits to all members of the
organization and to the society.(ISO).
10 Quality Management
SYSTEMS IN QUALITY MANAGEMENT
11 Quality Management
WHAT IS QUALITY
MANAGEMENT
12 Quality Management
6.50 6.55 7.00
13
THIS IS BECAUSE....
OF CERTAIN FACTORS WHICH
Affect the time he takes
He cannot control
Vary randomly
e.g. The traffic you encounter under normal course of travel
14
UNDER NORMAL SCHEME
OF OPERATION
Maximum deviation
Inherent
Variability
Aimed value
(white noise)
Minimum deviation
15
PROBABLY BECAUSE :
TODAY HE IS EARLY ! • His watch was running fast.
WHY ? • He got a lift.
• His bus driver took a shortcut.
• He stayed over in the colony.
• He had some important work to be finished
before 7.30.
16
GRAPHICAL DISPLAY OF
VARIABILITIES
CASE I
T
Assignable O
Assignable (Black noise)
Variability T
Variability A
L
Inherent
Variability
Aimed Value V
A
R
I
A
Assignable Assignable B
Variability Variability I
L
I
CASE II CASE III
T
Y
17
TYPES OF CAUSES
The variation which is due to natural variability (due to
background noise and cumulative effect of many small, essentially
uncontrollable causes) is called stable system of CHRONIC/
COMMON CAUSES
The occasional variation which may be present in the output of a
process and generally large when compared to the background
noise and usually Represents an unacceptable level of process
performance. This variation is Called ASSIGNABLE
/SPECIAL /SPORADIC CAUSES.
The process that is operating with only chance causes of variation
present is said to be in STATISTICAL CONTROL
A process that is operating in the presence of assignable causes is
said to be OUT OF CONTROL.
18
TYPES OF CAUSES
19
Total Process Variation
Common Cause Variation Special Cause Variation
nature System Deficiency Process Detail failure
Scope of Influence All production output are Not all production output
affected similarly are affected similarly
Sources Many small sources A few major sources
Process Behavior Stable and predictable Sporadic and unpredictable
Improvement action Requires fundamental Requires point of
change production change
Responsibility Management Supervisor/ Operators
20
Deming’s 14 Points for Management
21 Quality Management
W. EDWARD DEMING
1927 introduced to Shewhart in Bell Labs
From June–August 1950, Deming trained
hundreds of engineers, managers, and
scholars in statistical process control (SPC)
and concepts of quality
Deming Award
Deming’s 14 Points for Management
Deming’s 7 deadly disease
Deming’s System of Profound Knowledge
22 Quality Management
QUALITY CHAIN RECATION
23 Quality Management
Deming’s 14 Points for Management
1. Create constancy of purpose for improvement of Product and
services
9. Break down barriers between departments. (Everybody wins if the system wins)
11. Eliminate workstandards and numerical quotas(The focus is not on how many you
make, it is on how well you make them.)
12. Permit pride of workmanship (We need people to have pride in their work, not in
their ability to meet ratings)
14. Top management commitment and action for all above points
25 Quality Management
Deming’s 14 points for Management
26 Quality Management
JOSEPH M JURAN
28 Quality Management
JURAN TRIOLOGY
QUALITY PLANNING
The process for developing quality goals and a plan to meet them. It involves
understanding customer requirement and creating the process for meeting the
requirement
QUALITY CONTROL
On going measurement of process quality through measuring current performance
and the gap between performance and targets. Action steps are taken to close the
gaps and keep the process in statistical control.
QUALITY IMPROVEMENT
Identifying improvement projects based on quality control measurement, organizing
improvement teams, diagnosing and proposing solutions to the problem, proving
their effectiveness and implementing them with quality control measure in place for
the new process.
29 Quality Management
Juran’s Triology
Quality Planning Quality Control Quality Improvement
Determine who the Evaluate actual product Establish the infrastructure
Customers are performance
Determine the needs of the Compare actual performance Identify the improvement
customer to product goal projects
Develop product features Act on the difference Establish project Teams
that respond to customer’s
need
Develop processes able to Provide the teams with
produce the product feature resources, training and
motivation to:
Transfer the plans the (Diagnose the causes ,
operating forces Stimulate remedies,
Establish controls to hold the
gains)
30 Quality Management
Phillip Crosby
The Fun Uncle of Quality Management
FOUR ABSOLUTES OF QUALITY
32 Quality Management
KAORU ISHIKAWA
33 Quality Management
Japanese Approach to Quality
34 Quality Management
Cost of Quality
Joseph Juran first discussed cost of quality analysis in
1951 in the first edition of Quality Control Handbook.
Crosby’s categories
• Price of Conformance (POC/COC)
– Prevention costs
– Appraisal costs
• Price of Nonconformance (PONC/CONC)
– Internal defect costs
35 – External defect costs
Quality Management
PREVENTIVE COST
Costs relate to efforts to prevent failures. These are the costs that are
incurred on preventing a quality problem from arising. The cost of planning,
introduction and maintenance of a quality system, and costs of any action
taken to investigate, prevent or reduce non-conformities or defects would be
included in this category.
36 Quality Management
APPRAISAL COST
APPRAISAL COSTS relate to testing, execution an examination to assess
whether specified quality is being maintained. These are the costs that are
incurred in assessing that the products or service conform to the requirements.
costs can be contained or reduce when there is emphasis on quality
improvement. Also called Detection Cost.
Final Inspection
Drawing Checking
37 Quality Management
INTERNAL FAILURE COST
INTERNAL FAILURE COSTS: arise due to internal failures.
Such costs result from a product or service failing to meet the
quality requirement prior to delivery. These costs arise within
the organization because of the failure to achieve the specific
quality, before transfer of ownership to the customer.
38 Quality Management
EXTERNAL FAILURE COST
Pricing Errors
Penalties
39 Quality Management
COST OF POOR QUALITY CONTRIBUTION
Internal Failures 25 to 40 %
Appraisal 10 to 50%
Prevention .5 to 5%
Quality Management 40
Deming, Juran, Crosby on COQ
• Deming – the cost of nonconformance, and the
resulting loss of good will, is so high that
measuring it is not necessary
41 Quality Management
Something to think about
Net profits for many companies is less than 5% of sales
• COPQ on the average is 17% of sales
42 Quality Management
Process Capability
Six Sigma
The best performance:
VARIATION
1 1
68.27%
2 2
95.45%
3 3
99.73%
Do you mean to say, whether you like it or not, 99.73%
of the observations will lie within Average +/- 3 s.d.?
Characterization of the pattern
Variability is estimated through standard deviation.
Variation /
Standard deviation Mean or Average
Center / Location
Process capability refers to the natural variation of a process relative to the variation
allowed by the design specifications. It is defined as the ratio of the range of the design
specifications (the tolerance range) to the range of the process variation, which for
most firms is typically 6sigma.
Cp = Tolerance Range/ Process Range
Tolerances are design specifications reflecting customer requirements for a product.
They specify a range of values above and below a designed target value (also referred
to as the nominal value), within which product units must fall to be acceptable.
PROCESS CAPABILITY
Process Capability
= USL-LSL/6
Mean = 85.8
LSL USL
VARIATION
ACTUAL
PERFORMANCE
Vs.
SPECIFICATIONS
Or
Customer Requirements
PROCESS CAPABILITY
A second measure of process capability is the
process capability index (Cpk). The Cpk differs from
the Cp in that it indicates if the process mean has
shifted away from the design target, and in which
direction it has shifted—that is, if it is off center.
Exercise on Cp/Cpk
The Patanjali Food Company packages potato chips in bags.
The net weight of the chips in each bag is designed to be 9.0
oz, with a tolerance of +/- 0.5 oz.
The packaging process results in bags with an average net
weight of 8.80 oz and a standard deviation of 0.12 oz. The
company wants to determine if the process is capable of
meeting design specifications.
Interpretation of Cpk
Cpk < 1.00 Inadequate it indicates that the process is not adequate with
respect to the production tolerances
(specifications), and either process variation
needs to be reduced or process mean
1.33 < Cpk < 1.50 Satisfactory it indicates that process quality is adequate,
material substitution may be allowed, and no
stringent quality
control is needed.
1.50 < Cpk < 2.00 Excellent it indicates that process quality exceeds
"Satisfactory"
Actual vs Specified Comparison
6
Are you comfortable with the status quo? You want to reduce
the variability from to 1?
Reduce the variation by improving the process:
Are you comfortable with the status quo? You still want to
further reduce the variability from 1 to 2?
Reduce the variation by improving the process:
2 2 2 2 T=10 2
6 2
Tolerance(T)
LSL USL 0.6 ppm
Looking for reducing variability further 2 to 3 ?
Six Sigma without Shift:
Oh, Yes!
You have got it!!!
3 3 3 3
T=12 3
6 3 0.002 ppm
Tolerance(T) or 2 ppb
LSL USL
Wait a bit! Every time you are assuming that average has always
been maintain at target. Is it practical? What happens if the
average shifts to a distance of 1.5 3 from the target to the worse
side?
Process Shift
The reason for this discrepancy was determined by Motorola
in their early days in developing Six Sigma. Motorola
determined , through their own experience that process drifts
overtime and they referred to this phenomenon as “Long
Term Dynamic Mean Variation”. This variation generally
falls between 1.4 to 1.6 sigma.
Six Sigma with Shift (Short-term):
Let us assume, average can go as away as 1.5 times s.d.
from the target.
T=12 3
(with 1.5 3 shift)
3.4 ppm
4.5 3 1.5 3 1.5 3
Today we thought that
the sigma level to be of
6 3 Six, in the long run it
Tolerance(T)
LSL USL becomes 4.5 .
Six Sigma as a Goal
7
Yield = 1 –( 5 x 100 ) x 100