Ch 8: Measuring and Controlling Quality

Lakukan tugas rumah & ujian kamu dengan baik sekarang menggunakan Quizwiz!

Defects (or Errors) per Million Opportunities

(Number of defects discovered / opportunities for error) * 1,000,000

Cpu

(USL - u (process average))/ 3 sigma (upper one-sided index)

Process Capability Index (Cp)

(Upper Specification Limit (USL) - Lower Specification Limit (LSL) / 6 sigma (sigma being the standard deviation of the process)

Non-conformances per unit (NPU)

(or Defects per Unit in manufacturing) = Total number of non-conformances / Number of units inspected 260/100 = 2.6 NPU

Proportion nonconforming

(or Proportion Defective in manufacturing) = Number of nonconforming units found / Number of units inspected. Usually displayed as a percentage. For example: (8 / 100)*100 = 8%

Cpl

(u (process average) - LSL)/3 sigma (lower one-sided index)

One often uses judgement about the nature of operations and the costs involved in making these decisions.

1: If the cost of investigating an operation to identify the cause of an apparent out-of-control condition is high, wider control limits should be adopted. Conversely, if the cost is low, narrower limits should be selected. 2: If the cost of the defective output generated by an operation is substantial, narrower control limits should be uses. Otherwise, wider limits should be selected. 3: If he cost of both types of errors are significant, wide control limits should be chosen and a larger sample size should be used. Also, more frequent samples should be taken to reduce the duration of any out-of-control condition that might occur. 4: If past experience with an operation indicates that an out-of-control condition arises quite frequently, narrower control limits should be considered. In the event that the probability of an out-of-control condition is small, wider limits might be preferred.

When a process is in statistical control, the points on a control chart fluctuate randomly between the control limits with no recognizable pattern:

1: No points are outside of the control limits. 2: The number of points above and below the center line is about the same. 3: the points seem to fall randomly above and below the center line. 4: Most points, but not all, are near the center line, and only a few are close to the control limits.

Process Capability Study

A carefully planned study designed to yield specific information about the performance of a process under specified operating conditions.

Three types of studies are often conducted

A process characterization A peak performance study A component variability study

A Repeatability and Reproducibility (R&R) Study

A study in a measurement system using statistical analysis. This study can quantify the error, uncertainty or maximum resolution of a test or inspection system

Throughput Yield (TY)

An estimate of the number of units that have no non-conformances: TY = e^-NPU

Nonconformance

Any defect or error associated with a unit of work

Variable Measurement

Applies to dimensional quantities such as length, weight, time, or any other value on a continuous scale of measurement

When implementing SPC, practitioners must consider the four issues

Basis for Sampling Sample Size Sampling Frequency Location of Control Limits

The steps in a process capability study are similar to those of any systematic investigation, and include the following

Choose a representative machine or segment of the process Define the process conditions Select a representative operator Provide materials that are of standard grade, with sufficient materials for uninterrupted study Specify the gauging or measurement method to be used Collect the measurements and interpret the data

Several reason why high rates occur

Complexity Defect Rate Inspection Rate

Hugging the Center Line

Control limits may be too wide, or miscalculated

Location of Control Limits

Control limits need not adhere to the statistical "3 standard deviations" formula. It may be desirable to use wider or narrower control limits to reduce the costs associated with drawing the wrong conclusions

Practical Guidelines

Cost models attempt to find the best combination of SPC design parameters (center line, control limits, sample size, and sampling interval) that minimize expected cost or maximize expected profit.

($$) Appraisal Costs

Costs associated with efforts to ensure conformance to requirements, generally through measurement and analysis of data to detect non-conformances (inspections, which are costly

External Failure Costs

Costs due to customer complaints and returns Product recall costs and warranty claims Product liability costs

($$$) Internal Failure Costs

Costs incurred as a result of unsatisfactory quality found before the delivery of a product to the customer (this would be final inspection or final burn-in, quite expensive, since the product is now in its finished state)

Manufacturing classifications of defects

Critical Defect Major Defect Minor Defect

ISO 11462-1 standard addresses which elements

Definition of SPC goals Conditions for a successful SPC system Elements of the SPC system

Manufacturing, Variables Data

Diameters of machined ball bearings measured with a micrometer -> average diameter and the range of measurements (Statistical Process Control xbar and R-Chart) or standard deviation (Statistical Process Control x-bar and s-Charts) of a sample of ball bearings

Example of term indicator

For instance, though you cannot directly measure dissatisfaction, you can use the number of complaints or lost customers as indicators of dissatisfaction

Sudden shift in the Process Average

If eight consecutive points fall on one side of the center line, one could conclude that the mean has shifted

($) Prevention Costs

Investments made to keep non-conforming products from occurring and reaching the customer, including the following specific costs (designing in the quality in the product, this is usually the less expensive option)

Measurement System Evaluation

Low-technology instruments High-technology instruments Total observed variation in production output

Statistical Process Control (SPC)

Methodology for monitoring a process to identify special causes of variation and signal the need to take corrective action. SPC provides a means by which a firm can demonstrate its quality capability.

($,$$$) External Failure Costs

Occurs after poor-quality products reach the customer (this is the most expensive of all quality costs)

nonconforming Unit of Work

One unit of work that has one or more defects or errors

When special causes of variation are present, the process is said to be

Out of Control

Manufacturing, Attributes Data

Percentage of faucets that have cosmetic defects (Statistical Process Control Fraction Nonconforming (p) Chart)

Services

Percentage of orders filled accurately (Statistical Process Control Fraction Nonconforming (p) Chart), or the time taken to fill and ship a customer's order (Statistical Process Control x-bar and R-Chart)

For attribute data, the two important quality measures are

Proportion nonconforming Non-conformances per unit (NPU)

Prevention costs include (list)

Quality planning costs Process control costs Information systems costs Training and general management costs

When a worker or an inspector measures the same part multiple times the results will usually show some variability. Thus

Repeatability, or equipment variation (EV) Reproducibility, or appraiser variation (AV) A Repeatability and Reproducibility (R&R) Study

Internal Failure Costs includes (list)

Scrap and rework costs Costs of corrective action Downgrading costs Process failures

SMART, an acronym for good measurements

Simple (easy and cost-effective to obtain) Measurable (clear and un-ambiguous) Actionable (information to make good decisions for process management) Related (clearly related to what is important to customers - both external and internal - and for running the business)

When the variation in the process is due to common causes of variation alone, we say that the process is in

Statistical Control, or just Control

Definition of SPC goals

Such goals might include reducing variation around target values and compensating for process variation to ensure product conformity, reducing costs, indicating how the process is likely to behave in the future, and quantifying process capability

Sampling Frequency

Taking large samples on a frequent basis is desirable but clearly not economical. Samples should be close enough to provide an opportunity to detect changes in process characteristics as soon as possible and reduce the chances of producing a large amount of non-conforming output. However, they should not be so close that the cost of sampling outweighs the benefits that can be realized.

Appraisal Costs

Test and inspection costs Instrument maintenance costs Process measurement and control costs

First wrong conclusion

The belief that a special cause is present when in fact one does not exist

Process Capability

The capability of a process to produce output that conforms to specifications

Sample Size

The choice of sample size represents a trade-off between cost and information. Small sample sizes reduce costs associated with the time that workers must spend collecting data; however, they provide less statistical information. Large samples are more costly but allow smaller changes in process characteristics to be detected with higher probability

Precision

The closeness of repeated measurements to each other. Precision relates to the variance of repeated measurements

Accuracy

The difference between the true value and the observed average of a measurement

Complexity

The number of defects caught by an inspector decreases with more parts and less orderly arrangement

Unit of Work

The output of a process or an individual process step

Attribute Measurement

The presence or absence of non-conformances in a unit of work, or The presence or absence of non-conformances in a unit of work, or the number of non-conformances in a unit of work. Often collected by visual inspection and expressed as proportions and counts. Collecting attribute data is usually easier because an assessment can usually be done more quickly by a simple inspection or count, whereas variable data require the use of some type of measuring instrument. However, attribute measurement requires a much larger sample size than variable measurement to obtain the same amount of statistical information. This difference can become significant when inspection of each item is time-consuming or expensive

Basis for Sampling

The purpose of a control chart is to identify the variation in a system that may change over time. In determining the method of sampling, samples should be chosen to be as homogenous as possible so that each sample reflects the system of common causes or assignable causes that may be present at that point in time. Also, the chance of observing differences between samples should be high, the chance of observing differences within a sample should be low. Samples that satisfy these criteria are called rational subgroups

Repeatability, or equipment variation (EV)

The variation in multiple measurements of a quality characteristic by an individual worker or inspector using the same instrument. Repeatability indicates how consistent a measuring instrument is. It is influenced by the condition of the measurement instrument, environmental conditions such as noise or lighting, the workers overall health and eyesight, and the process used to take the measurement such as how the part is positioned in the gage

Reproducibility, or appraiser variation (AV)

The variation when using the same measuring instrument by different individuals to measure the same parts. Reproducibility indicates how consistent workers or inspectors are in using measurement instruments. It is influenced by the training of workers in the use of the instrument, clarity of the directions or procedures of the measurement process, calibration of gages between workers, gage maintenance, and worker health

Measurement System

The workers who take the measurements + the instructions they use + the instruments they use

Elements of the SPC system

These address the processes an organization should implement and actions it should take to ensure that a successful SPC system includes both operational sand support activities. These elements include a process documentation and control plan, definition of process targets and limits, data collection, measuring equipment, data recording and analyses, process control, short- and long-term process capability assessment, communication of results, and process improvement implementation and project management activities

Conditions for a successful SPC system

These conditions include integration with a formal quality management system, management support, use of information for data-driven decisions and management reviews, and ensuring the competence of those who will be using the tools.

Process Performance Indexes

Used if the process include special causes of variation, which represents the actual, rather than the ideal, performance in a non-controlled environment. In reality, this makes little sense; many experts do not recommend this because it is important to control a process and remove special causes in order to achieve high levels of quality and customer satisfaction

SPC was first proposed by

Walter Shewhart in the 1920s

Second wrong conclusion

When special causes are present but are not signaled in the control chart.

Defect Rate

When the product defect is low, inspectors tend to miss more defects than when the defect rate is higher

Defect

a term most often used in Manufacturing

Error

a term most often used in Services

Measurements must be both

accurate and precise

Cycles

are short, repeated patterns in the chart, alternating high peaks and low valleys

Costs of corrective action

arising from time spent determining the causes of failure and correcting production problems

A component variability study

assesses the relative contribution of different sources of total variation. A component variability study uses a designed experiment to evaluate the sources of variability

Test and inspection costs

associated with incoming materials, work-in-process, and finished goods, including equipment costs and salaries (inspectors, supervisors, quality managers and quality engineers)

Efficient national and international trade requires weights and measures organizations that

assure uniform and accurate measures used in trade, national or regional measurement standards laboratories, standards development organizations, and accredited and internationally recognized calibration and testing laboratories

How can Complexity, Inspection Rate, and Inspection Rate be mitigated?

by using automated technology, or minimizing the number of quality characteristics that must be inspected, reducing time pressures, using repeated inspections by other inspectors, and improving the design of the workspace to facilitate the inspection task

SPC relies on

control charts

Product recall costs and warranty claims

cost of repair or replacement as well as associated administrative costs

Process control costs

costs spent on analyzing production processes and implementing process control plans

High-technology instruments

depend on modern electronics, microprocessors, lasers or advanced optics

A peak performance study

determines how a process performs when only common causes of variation are present. Typically this is done over a short time interval under carefullycontrolled conditions.

Instrument maintenance costs

due to calibration and repair of measuring instruments

Good data and measurement systems are the basis for

effective quality control as well as for quality improvement.

Accuracy is measured as the amount of

error in a measurement in proportion to the total size of the measurement

Information systems costs

expended to develop data requirements and measurements

The lack of accuracy reflects a systematic bias in the measurement such as

gage that is not properly calibrated, worn, or used improperly by the worker

Metrology is also vital to

global competitiveness

Quality control seeks to ensure that processes perform in a stable and predictable fashion by

identifying when corrective action is needed

Training and general management costs

including internal and external training programs, clerical staff expenses, and miscellaneous supplies

Managers usually react to high failure costs by

increasing inspection

If special causes are present, the control chart will

indicate them, and corrective action can be taken quickly

Process Capability (indexes)

is measured by computing numerical indexes. The distribution of process output (length, time, weight, etc.) can differ in both location and spread relative to the specifications

Cp

is the ratio of the specification range to the process variation.

if the variation in the measurement system is high

it is difficult to separate the true variation in the process from the variation in the measurement system, resulting in misleading conclusions about quality

The overall increase of inspection typically results of

little, if any, improvement in overall quality or profitability

Quality costs are the responsibility of

management

Low-technology instruments

manual devices such as gages and rulers

Scrap and rework costs

material, labor, and overhead

Many government regulations (such as those in Drugs, Biologics, and Medical Devices) and commercial contracts require regulated organizations or contractors to verify that

measurements are traceable to a reference standard.

Timely

measurements need to be available and communicated to workers and managers when they need the results from the measurements

Cpk

minimum (Cpu or Cpl)

Metrology is the science

of measurement and is defined broadly as the collection of people, equipment, facilities, methods, and procedures used to assure the correctness or adequacy of measurements

Major Defect

one not critical but likely to result in failure or to materially reduce the usability of the unit for its intended purpose

Minor Defect

one not likely to materially reduce the usability or the item for its intended purpose, nor have any bearing on the effective use or operation of the unit.

Critical Defect

one that judgement and experience indicate will surely result in hazardous or unsafe conditions for individuals using, maintaining, or depending on the product and will prevent proper performance of the product

Metrology is vital in

our daily lives

Low precision is the result of

random variation that is built into the instrument, such as friction among its parts

Product liability costs

resulting from legal actions and settlements

Costs due to customer complaints and returns

rework on returned items, cancelled orders, and freight premiums

A control chart is

run chart to which two horizontal lines, called control limits are added; the Upper Control Limit (UCL) and the Lower Control Limit (LCL).

Quality planning costs

salaries of individuals associated with quality planning and problem-solving teams, the development of new procedures, new equipment design, and reliability studies

Most control charts today are implemented via

software; nevertheless, they are quite easy to do by hand

Thus, an objective of quality assurance is to minimize measurement error. In many industries, in-process measures are collected through

some type of manual inspection process. Processes that rely on visual interpretation of product characteristics or manual reading of gauges and instruments may encounter error rates of from 10 to 50 percent

A process characterization

study is designed to determine how a process performs under actual operating conditions, which may include both common and special causes of variation. It is typically performed over a moderately long time interval to capture any and all variations that might occur

Downgrading costs

such as revenue lost when selling a product at a lower price because it does not meet specifications

The difference between Accuracy and Precision is often illustrated by

target

The term indicator is often used for measurements

that are not a direct or exclusive measure of performance

Measurement is

the act of collecting data to quantify the values of product, service, process, and other business metrics

The only information needed to conduct a process characterization study is

the mean, standard deviation, and histogram of a sample of measurements

If there is little variation in the measurement system

the observed measurements reflect the true variation in the process

Trends

the result of some cause that gradually affects the measurement and causes the points on a control chart to gradually move up or down

Control limits are chosen statistically

to provide a high probability that points will fall between these limits if the process is in control.

Measures and indicators refer

to the numerical results obtained from measurement

Total observed variation in production output

true process variation + variation due to measurement

dashboards

typically consist of a small set of measures (five to six) that provide a quick summary of process performance

Process failures

unplanned machine downtime or unplanned equipment repair

The ISO standard ISO 11462-1 provides guidance for organizations wishing to

use SPC to meet statistical methods

In practice, an increase in prevention

usually generates larger savings in all other cost categories

Calibration is the process of

verifying the capability and performance of an item of measuring and test equipment compared to traceable measurement standards

To evaluate the Process Capability

we need the specifications for the output, and statistical information about the actual process performance

Process measurement and control costs

which involve the time spent by workers to gather and analyze quality measurements


Set pelajaran terkait

Chapter 32 Environmental Emergencies

View Set

*OB Quiz 1 Possible Questions- Chapters 1-5

View Set

Why was Cortez able to conquer the Aztec Empire? What important goods were involved?

View Set

Ch 15 Endometriosis and Adenomyosis

View Set

Chapter 6 Meiosis is the basis of sexual reproduction

View Set

AP Biology Unit 7 Introduction to Natural Selection

View Set