Cost of Quality - 3 September, 2010 - Dr. Paramjit Kaur
Cost of Quality - 3 September, 2010 - Dr. Paramjit Kaur
Cost of Quality - 3 September, 2010 - Dr. Paramjit Kaur
ASSIGNMENT
COST OF QUALITY
SUBMITTED TO:
SUBMITTED BY:
DHEERAJ AGGARWAL KRITI SINGHAL PANKAJ JUNEJA SANCHIT AGARWAL SONALI SHARMA
Content 1) 2) 3) 4) 5) 6)
Introduction ..03 Quality ..03 Quality Control ..04 Evolution of cost of quality ..07 Cost of Quality Models ..07 P-A-F Method ..08 a) Prevention Costs ..08 b)Appraisal Costs ..08 c) Failure Costs ..09 I)Internal Failure ..09 ii)External failure Costs ..09 7) Total Quality Cost ..10 8) Crosbys Model ..11 9) Opportunity and Intangible Costs ..11 10) Team Approach Method ..13 11) Process Cost Model ..13 12) Activity Based Quality Model ..14 13) Techniques to Measure Cost Of Quality ..15 a) Control Chart ..15 b) Control Limit ..15 c) Pareto Diagram ..16 i) Count Pareto ..16 ii) Cost Pareto ..16 d) Cost and effect diagram ..17 14) Typical Uses ..20 15) Typical Results Achieved ..21 16) Typical Symptoms ..22 17) Typical Problems Encountered ..23 18) Things to Consider Before Implementing Cost of Quality (COQ).24 19) Quality Management ...26 20) Cost of Poor Quality ...29 21) Reducing the Failure of Cost of Quality ....30 22) Defect Removal Activities 30 23) Goal of Cost of Quality 32 24) Companies Visited 33 i) Mahindra & Mahindra 33 ii) Rana Polycot Ltd. 39 iii) Sigma Freudenberg Nok Pvt. Ltd.....................42 iv) Maruti Suzuki Ltd. 46 v) Parabolic Drugs Limited 49
INTRODUCTION
Quality has become so important to success that currently many prestigious, internationally recognized awards are given to companies for quality by nearly every country and many professional organizations. For example, the Malcolm Baldrige Quality Award, created by the United States Congress in 1987, recognizes US firms with outstanding records of quality improvement and quality management. The Deming Prize created in Japan by the Japanese union of scientists and engineers long before the Baldrige Quality Awards is awarded to companies around the world that excel in quality improvement. The international Organization for Standardization, based in Europe, has developed international standards for quality management called ISO 9000. The ISO standards first gained popularity in Europe but are now global guidelines for the design, development, production, final inspection and testing, installation, and servicing of products, processes, and services. To be certified, a company must document its quality systems and pass a rigorous third-party audit of its manufacturing and customer- service processes. Organizations proudly display their quality awards and certificates as evidences of their commitment to product and services quality. Many organizations have adopted Baldrige or Deming prize criteria as their internal quality management guidelines even if they do not seek to win a prize for their efforts. TCSI, for example, has adopted criteria from both the Baldrige and Deming awards and has obtained ISO 9000 certification. The company does not plan to apply for any awards, however, because CEO Cooper and CFO Freeman believe the prizes themselves are unnecessary to the companys success and that the lengthy application and evaluation processes would distract the growing business. Freeman would rather spend his time managing TCSIS quality than applying for quality prizes. QUALITY Quality means getting everyone to do what he or she has agreed to do and do it right the first time. Quality is an effective system of integrating quality improvement efforts of various groups of the organization so as to provide products or services at a level at which all customers are satisfied. Quality is defined as a process of matching or achieving the standard already laid down for various functions or services. This can be brought about by Total Quality Management
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(TQM). Deming and Juran have defined TQM as the strategic commitment to improve quality by combining statistical quality control methods with a cultural commitment to seeking incremental improvements that increase productivity and lower cost. Quality is something which is complex and varies from one industry to another. Quality needs to be model on the basis of customer need, context of the market, industrial goals, system requirements etc. Quality gurus have given definitions that cover the meaning of quality. Some of them have been considered as the starting point to define quality, for example the definitions given by Philip Crosby and Joseph M. Juran. Still the major problem with software engineering is that the term quality cannot be defined with absolute clarity. The experts disagree both on the definition of quality and how to achieve it. Quality is the conformance to requirements. Requirements must be clearly stated so that people involved can clearly understand that. Then in the development process, measurements are taken continually to determine conformance to those requirements. The non-conformance will be treated as absence of quality or defect. Quality of a good is its Fitness for use.Customer requirements and expectations involves whether the products or service fit for their uses. Since the different customer may use the products in different ways, it means that products must possess multiple elements of fitness for use. Each of these elements is a quality characteristic and they can be categories into two types that is quality of design and quality of conformance.
QUALITY CONTROL
The purpose of quality control is to uncover defects and have them corrected so that defect-free products will be produced. Quality control is limited to looking at products. It is a function that should be performed by the workers. Tasks such as systems reviews and software testing are quality control tasks. In other words Quality control is operational techniques and activities that are used to fulfill requirements for product quality. It involves techniques that monitor a process and eliminate causes of unsatisfactory performance at all stages of the quality loop. Quality Control (QC), in real meaning, relates to the inspection of finished goods prior to shipment.
In the usual term in manufacturing, QC involves taking a sample of finished goods from an assembly line, testing them for quality, and extrapolating the general quality of the production run from the quality of that sample. Quality Control is also about monitoring a process to determine if the standards set for the process were being followed (such as for an assembly line). In software applications, this term tends to take on the role of referring to the testing of the application. In the IT world, still many IT professionals think Quality Control to be same as software Testing. This concept can be workable if the word "testing" is broadened out to include executable (source code) and non-executable (artifacts) aspects of a product. QualityControl tends to find the defects in a product by a monitoring, audit, and assessment of process. Quality Testing is then considered the procedures by which those defects are actually found. Thus, that is why some people make the distinctions between quality control and quality testing. The latter tends to be the "find-and-isolate" procedure and the former tends to be the "monitor-and-assess" procedure. In other words, one might say that Quality Control is used as a feedback mechanism for the Quality Testing process. Both of which are derived from the Quality Assurance process, which dictates the actions of the Quality Test and Quality Control procedures. Quality control is used to verify that deliverables are of acceptable quality and that they meet the completeness and correctness criteria that were established in the quality planning process. If no such criteria were established, then this becomes more of an ad hoc process. The Cost of Quality is often referred to as the cost of doing things wrong. Every time a business makes a mistake it costs money to make the mistake and then correct it. The cost of doing it wrong is the hit; the activities to correct it usually match that which should have been done correctly so dont count. Well, not directly anyway but fixing the issue could have impacts that push the Cost of Quality up.
Cost of quality can be defined as all the costs attributable to the production of quality which is not 100 percent perfect. Murthy (1983) and CEM (1996) classify costs of quality into the following types: Appraisal Costs, which are the costs of inspection, testing and other tasks to ensure that the product or process is acceptable, prevention costs, which are the sum of all costs to prevent defects, internal failure are the costs incurred within the system and external failure costs that are costs of defects that pass through the system.
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Quality Costs represent the difference between the actual cost of a product or service and what the reduced cost would be if there were no possibility of substandard service, failure of products, or defects in their manufacturing. Improving quality is considered by many to be the best way to enhance customer satisfaction, to reduce manufacturing costs and to increase productivity. Any serious attempt to improve quality must take into account the costs associated with achieving quality, since nowadays it does not suffice to meet customer requirements, it must be done at the lowest possible cost as well. This can only happen by reducing the costs needed to achieve quality, and the reduction of these costs is only possible if they are identified and measured. The identification itself is not straightforward because there is no general agreement on a single broad definition of quality costs. However, CoQ is usually understood as the sum of conformance plus non-conformance costs, where cost of conformance is the price paid for prevention of poor quality (for example, inspection and quality appraisal) and cost of nonconformance is the cost of poor quality caused by product and service failure (for example, rework and returns). "Highest quality is lowest cost" is a Japanese manufacturing aphorism based on the premise that the highest quality manufacturer will earn a reputation that makes buyers prefer, price being reasonably similar, to buy its goods. This means that the manufacturer will produce more than its competitors, and thus will both have economies of scale and be able to accept a lower profit per unitthus the highest quality goods will have a lower cost by driving other goods from the market. The production of higher quality goods can also reduce quality costs. From the purchaser's point of view the highest quality goods will have the fewest problems, and the cost of dealing with a problem far outweighs the extra purchase cost. The Cost of Quality ("COQ") measurement can track changes over time for one particular process, or be used as a benchmark for comparison of two or more different processes (eg. two machines, different production lines, sister plants, two competitor companies, etc.). Usually, Cost of Quality ("COQ") is measured in currency (eg. $), requiring all losses and wastes to be converted to their liquidated cost equivalent (i.e. man-hrs lost or spent are converted to $ by multiplying by the hourly rate, $/hr).
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Why is Cost of Quality ("COQ") Important? Cost of Quality ("COQ") can be used to identify the global optimum for a process, and monitor that process' progress towards its global optimum. Global optimum is defined as the best possible outcome from all physically possible operating modes, combinations, and permutations of the current process.
P-A-F METHOD
The traditional P-A-F method suggested by Juran (1951) and Feigenbaum (1956) classifies quality costs into prevention, appraisal and failure costs. Prevention costs are associated with actions taken to ensure that a process provides quality products and services, appraisal costs are associated with measuring the level of quality attained by the process, and failure costs are incurred to correct quality in products and services before (internal) or after (external) delivery to the customer.
PREVENTION COSTS are those associated with preventing defects before they happen. This is a proactive approach to defect prevention rather than defect correction and removes the idea of quality efforts essentially being reactive in efforts to "put out fires." Prevention costs involve investments aimed at getting work done right the first time and preventing quality problems from ever coming up, as far as it is possible. It is long-term strategy adopted by the organization for the continuous improvement in their processes. The elimination of the rework goes hand in hand with increase in quality, and decreases in schedule and cost; this is the fastest, cheapest, and highest approach to building software. They include:
Staff Training Requirement Analysis Fault-Tolerant Design Defensive Programming Usability Analysis Clear Specification Accurate internal communication
APPRAISAL COSTS include cost incurred in detecting the error. Appraisal techniques are used for the verification and validation. These techniques help organization to increase in quality with lesser cost. Examples of appraisal costs include code inspections, testing, software design reviews. They may be summarized as:-
Design review Code inspection Usability Testing Calibration cost Laboratory expenses
FAILURE COSTS: The cost resulting from products or services not conforming to requirements or needs of the customer. Failure costs are divided into A. Internal failure costs and B. External failure costs.
INTERNAL FAILURE COSTS: Failure costs occurring prior to delivery or shipment of the product, of finishing of a service to the customer. Examples are the costs of: Scraps and rejects Repair and Rework Downtime Bug fixes Wasted in-house user time Wasted tester time Wasted marketer time Wasted advertisements Direct cost of late shipment Opportunity cost of late shipment Retesting Material review Sales and discounts for inferior product
EXTERNAL FAILURE COSTS: Failure costs occurring after delivery of shipment of the product and during or after furnishing of a service to the customer. Examples are the costs of:
Warranty costs and Off warranty repairs and replacement Customer complaints Product liability Transportation losses Technical support calls Preparation of support answer books Refunds and replacement with updated product Lost sales Lost customer goodwill Costs imposed by law Customer returns
TOTAL QUALITY COSTS: It is the sum of the above costs. It represents the difference between the annual cost of a product or service and what the reduced cost would be if there were no possibility of substandard service, failure of products or defects in their manufacture. Most COQ systems are defined by use of 4 categories of costs: COQ Category Typical Descriptions (may vary between different Organizations) Costs associated with internal losses (i.e. within the process being analyzed) Costs external the process being analyzed (i.e. occur outside, not discovered External within). by, or These costs affect third are usually parties (eg. customer complaints, latent defects found by the
Internal
customers). Some External costs may have originated from within, or been caused, created by, or made worse by the process being analyzed. They are defined as External because of where they were discovered, or who is primarily or initially affected.
customer, warranty
Costs associated with the prevention of future planning, mistakePreventive losses: (eg. unplanned or undesired problems, losses, proofing, scheduled lost opportunities, breakdowns, work stoppages, waste, maintenance, quality etc.) assurance KPI's, inspection, quality check, dock audits, third Assessment Costs associated with measurement and assessment of party audits, measuring the process. devices, reporting systems, data collection systems, forms COQ systems are sometimes assisted by specially designed COQ Software
CROSBYS MODEL
The cost categories of Crosbys model (Crosby, 1979) are similar to the P- A-F scheme. Crosby sees quality as conformance to requirements, and therefore, defines the cost of quality as the sum of price of conformance and price of non-conformance (Crosby, 1979). The price of conformance is the cost involved in making certain that things are done right the first time and the price of non-conformance is the money wasted when work fails to conform to customer requirements.
Several references propose CoQ models that include the additional category of intangible costs. These are costs that can be only estimated such as profits not earned because of lost customers and reduction in revenue owing to non-conformance. The importance of opportunity and intangible costs for quality costing has been describe a less formal method based on collecting quality costs by department.
Cost area
Examples Materials scrapped or junked Labor and burden on product scrapped or junked Labor, materials, and burden necessary to effect repairs on salvageable product Extra operations added because of presence of defectives Burden arising from excess production capacity necessitated by defectives Excess inspection costs
Discount on seconds Tangible costs sales accounts Customer complaints Charges to quality guarantee account Delays and stoppages caused by defectives Customer good will Loss in morale due to friction between Intangible costs Departments
Existing accounting systems are usually considered as poorly fitted for generating reports on quality measurements .They do not provide appropriate quality related data, and benefits
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resulting from improved quality are not measured .Although most CoQ measurement methods are activity/process oriented, traditional cost accounting establishes cost accounts by the categories of expenses instead of activities. Thus, many CoQ elements need to be estimated or collected by other methods.
There is no consensus method on how to allocate overheads to CoQ elements adequate method to trace quality costs to their sources.
and
no
An activity-based costing (ABC) model was developed by Cooper and Kaplan to solve this problem. Under ABC, accurate costs for various cost objects b y t r a c i n g r e s o u r c e c o s t s t o their r e s p e c t i v e activities and the cost of activities to cost objects a r e a c h i e v e d . The ABC approach is actually not a CoQ model. It is an alternative approach that can be used to identify, quantify and allocate quality costs among products, and therefore, helps to manage quality costs more effectively. The long- term goal of ABC systems is to eliminate non-value added activities and to continuously improve processes, activities and quality so that no defects are produced.
No matter which quality costing approach is used, the main idea behind the CoQ analysis is the linking of improvement activities with associated costs and customer expectations, thus allowing targeted action for reducing quality costs and increasing quality improvement benefits.
Therefore, a realistic estimate of CoQ, which is the appropriate tradeoff between the levels of conformance and non-conformance costs, should be considered an essential element of any quality initiative and a crucial issue for any manager. A number of organizations are now seeking both theoretical advice and practical evidence about quality related costs And the implementation of quality costing systems.
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Statistical quality control (SQC), which is also called statistical process control (SPC), is a formal means of distinguishing between random and non-random variations in an operating process. A control chart, one of the tools in SQC, is a graph of a series of successive observations of a particular step, procedure, or operation taken at regular intervals of time. It indicates upper and lower statistical control limits, and an average line, for samples or subgroups of a given process. If all points on the control chart are within the limits, variation may be ascribed to common causes and the process is deemed to be "in control." If points fall outside the limits, it is an indication that special causes of variation are occurring, and the process is said to be "out of control." Control Limit: A statistically-determined line on a control chart used to analyze variation within a process. If variation exceeds the control limits, then the process is being affected by special causes and is said to be "out of control." A control limit is not the same as a specification limit.
If analysis of the control chart indicates that the process is currently under control (i.e. is stable, with variation only coming from sources common to the process) then data from the process can be used to predict the future performance of the process. If the chart indicates that the process
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being monitored is not in control, analysis of the chart can help determine the sources of variation, which can then be eliminated to bring the process back into control. A control chart is a specific kind of run chart that allows significant change to be differentiated from the natural variability of the process. The control chart can be seen as part of an objective and disciplined approach that enables correct decisions regarding control of the process, including whether or not to change process control parameters. Process parameters should never be adjusted for a process that is in control, as this will result in degraded process performance. PARETO DIAGRAM Observations outside control limits serve as inputs for Pareto diagrams. A Pareto diagram is a simple bar chart that ranks related measures in decreasing order of occurrence. The principle was developed by Vilfredo Pareto, an Italian economist and sociologist who conducted a study in Europe in the early 1900s on wealth and poverty. The purpose of a Pareto diagram is to separate the significant aspects of a problem from the trivial ones. By graphically separating the aspects of a problem, a team will know where to direct its improvement efforts. Reducing the largest bars identified in the diagram will do more for overall improvement than reducing the smaller ones. There are two ways to analyze Pareto data depending on what you want to know: COUNT PARETO: Use this type of Pareto analysis to learn which category occurs most often, you will need to do a counts Pareto diagram. To create a counts Pareto, you will need to know the categories and how often each occurred. COST PARETO: Use this type of Pareto analysis if you want to know which category of problem is the most expensive in terms of some cost. A cost Pareto provides more details about the impact of a specific category, than a count Pareto can. For example, suppose you have 50 occurrences of one problem and 3 occurrences of another. Based on a count Pareto, you would be likely to tackle the problem that occurred 50 times first. However, suppose the problem that occurred 50 times costs only $.50 per occurrence ($25 total) and the problem that occurs 3 times costs $50 each time ($150 total). Based on the cost Pareto, you may want to tackle the more
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expensive problem first. To create a cost Pareto, you will need to know the categories, how often each occurred, and a cost for each category.
CAUSE & EFFECT DIAGRAMS The Cause & Effect (CE) diagram, also sometimes called the fishbone diagram, is a tool for discovering all the possible causes for a particular effect. The effect being examined is normally some troublesome aspect of product or service quality, such as 'a machined part not to specification', 'delivery times varying too widely', 'excessive number of bugs in software under development', and so on, but the effect may also relate to internal processes such as 'high rate of team failures'. The major purpose of the CE Diagram is to act as a first step in problem solving by generating a comprehensive list of possible causes. It can lead to immediate identification of major causes and point to the potential remedial actions or, failing this, it may indicate the best potential areas for
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further exploration and analysis. At a minimum, preparing a CE Diagram will lead to greater understanding of the problem. The CE Diagram was invented by Professor Kaoru Ishikawa of Tokyo University, a highly regarded Japanese expert in quality management. He first used it in 1943 to help explain to a group of engineers at Kawasaki Steel Works how a complex set of factors could be related to help understand a problem. CE Diagrams have since become a standard tool of analysis in Japan and in the West in conjunction with other analytical and problem-solving tools and techniques. CE Diagrams are also often called Ishikawa Diagrams, after their inventor, or Fishbone Diagrams because the diagram itself can look like the skeleton of a fish. The steps for using cause and effect diagrams are as follows: The problem under investigation is described in a box at the head of the diagram. A long spine with an arrow pointing towards the head forms the backbone of the "fish." The direction of the arrow indicates that the items that feed into the spine might cause the problem described in the head. A few large bones feed into the spine. These large bones represent the main categories of potential causes of the problem. Again, the arrows represent the direction of the action; the items on the larger bones are thought to cause the problem in the head. The smaller bones represent deeper causes of the larger bones they are attached to. Each bone is a link in a Cause-and-Effect chain that leads from the deepest causes to the targeted problem.
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Quality processes cannot be justified simply because "everyone else is doing them" - but return on quality (ROQ) has dramatic impacts as companies mature. Research shows that the costs of poor quality can range from 15%-40% of business costs (e.g., rework, returns or complaints, reduced service levels, lost revenue). Most businesses do not know what their quality costs are because they do not keep reliable statistics. Finding and correcting mistakes consumes inordinately large portion resources. Typically, the cost to eliminate a failure in the customer phase is five times greater than it is at the development or manufacturing phase. Effective quality management decreases production costs because the sooner an error is found and corrected, the less costly it will be.
No matter which quality costing approach is used, the main idea behind the CoQ analysis is the
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linking of improvement activities with associated costs and customer expectations, thus allowing targeted action for reducing quality costs and increasing quality improvement benefits.
Therefore, a realistic estimate of CoQ, which is the appropriate tradeoff between the levels of conformance and non-conformance costs, should be considered an essential element of any quality initiative and a crucial issue for any manager. A number of organizations are now seeking both theoretical advice and practical evidence about quality related cost and the implementation of quality costing systems.
Typical Uses Cost of Quality ("COQ") is used to collect cost data on a sampling basis (eg. all data occurring during a 24 hr period, calculated once each quarter), or on a continuous basis (eg. Cost of Quality ("COQ") is calculated with all data occurring in the month, and reported monthly). After confirming that the data is accurate and comprehensive, and consistent with previous definitions and implementations, it is analyzed for opportunities and trends. Based upon statistical analysis (eg. regression analysis, indexes, correlations, Pareto analysis, factor analysis, etc.), conclusions and recommendations are presented to managers of the process being analyzed. In some cases (supported by process modeling, heuristics, prior experience, or intuition) the optimum Cost of Quality ("COQ") can be predicted, and the process design necessary for achieving this global optimum Cost of Quality ("COQ") can be defined. A plan can then be defined to modify the current process, phase by phase, so as to move towards this global optimum process. Management responsible for the process can decide on if, how, and when they will run the current process, or modify the process for even better results. All projects are analyzed for their impact on Cost of Quality ("COQ"), and projects that show high ROQ are implemented on a priority basis (ROQ%= $Cost of Quality ("COQ") savings/$Implementation cost*100%). COQ Software is
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often used to enhance the COQ data collection, reduce the cost of running a COQ system, and ensure excellent data as fast and cheap as possible. Typical Results Achieved When all costs are included, Cost of Quality ("COQ") as a % of gross sales $ will probably be around 30% to 35% for a profit orientated organization, 40% to 60% for a not-for-profit organization (i.e. hospitals, charities, government, etc.). Many organizations take only a sub-set of the costs, including only those that tend to fluctuate, or that often need management intervention. The others are assumed to be constant. When manufacturing companies often earn only 5% NPBT (Net Profit Before Tax), a 35% Cost of Quality ("COQ") indicates that 40% of gross revenue is generated by the company as profit, but only 5% of that gets trapped as NPBT. Therefore, the profit yield is only 12.5% (87.5% of the available profit is lost before it gets to the bank). For improvements in Cost of Quality ("COQ"), some manufacturers have been able to reduce manufacturing costs by as much as 7.65% per year, every year, for more than 10 years. For Six Sigma processes, Cost of Quality ("COQ") is usually reduced to less than 1% of gross sales $. This indicates that, as large and unbelievable as Cost of Quality ("COQ") $ seems to most managers, it is a real number that can be eliminated through hard work and dedication. Obviously, as more and more improvements are made, it becomes more difficult to find the next saving. This is when an excellent Cost of Quality ("COQ") system can help point out the remaining opportunities.
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Currently have no Cost of Quality ("COQ") system, but could benefit from a welldesigned & implemented Cost of Quality ("COQ") system
Have a Cost of Quality ("COQ") system, but that Cost of Quality ("COQ") system is poorly designed, or poorly implemented.
Slow rate of improvement Low or no profitability Bureaucracy or complexity of business processes continue to get worse and worse Changes in one area tend to have disastrous effects in other areas Management get personally involved in quality problems only during a major crisis Management is running out of ideas on where to cut costs any further All employees are not actively and personally involved in driving the Organization's Mission forward
Many individuals and departments disagree on what are the top priorities for the Organization
Sub-processes and Departments are operated in a manner that is detrimental to the Organization's overall best interest.
For organizations not using COQ Software, there are often higher costs for running the COQ system, inconsistent implementation, and non-optimum results from the COQ system.
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Typical Problems Encountered Because of poor design or poor implementation of Cost of Quality ("COQ") systems, the Cost of Quality ("COQ") systems often suffer from one or more of the following problems:
COQ data collection is watered-down, or has superficial implementations that quickly become make-work exercises with little or no benefit, other than to fill filing cabinets or hard disk drives on computers.
Efforts are directed at where it is easy to collect data, or easy to implement changes, instead of focusing on the Cost of Quality ("COQ") priorities (eg. largest cost category, most variation, largest business risk, etc.)
The Cost of Quality ("COQ") input data are often incomplete. The Cost of Quality ("COQ") definitions are often un-clear, or not fully understood, resulting in varying interpretation and implementation over time. This variability tends to add significant noise to the Cost of Quality ("COQ") data, clouding the interpretation and hiding significant trends for extended periods of time.
Management does not actively use the Cost of Quality ("COQ") data in an effective manner. Decisions are often made without neither realizing nor considering the impact on Cost of Quality ("COQ"), thereby neutering the Cost of Quality ("COQ") system to irrelevancy.
When Cost of Quality ("COQ") is not utilized during project approval decisions, as management makes changes (supposed "improvements"), Cost of Quality ("COQ") $ tend to shift from one category to another, with little net effect. For example, a new machine is purchased to reduce scrap. Higher setup, first-off, inspection, and maintenance costs offset the scrap savings, with no net improvement in Cost of Quality ("COQ").
Cost of Quality ("COQ") costs oscillate between the four Cost of Quality ("COQ") categories on a revolving basis, with little or no reduction in the total Cost of Quality
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("COQ"). For example, money is spent to increase surveillance, which indicates a problem exists with internal &/or external failure costs. Surveillance costs are stopped, but prevention actions are taken to reduce failure costs, thereby increasing prevention costs. The preventive actions are not comprehensive or not consistently implemented, so the internal and/or external failures eventually come back. The rising internal &/or external failures prompt another round of surveillance activities, with additional assessment costs incurred.
The collection of Cost of Quality ("COQ") data becomes more and more costly and bureaucratic over time, making it slower to respond to significant changes, and less useful.
Statistical analysis of Cost of Quality ("COQ") data is not performed. Early recognition of trends is missed, and random variations are mistaken for significant signals; starting "wild goose" chases, wasting time & resources, and distracting everyone from the real issues.
Cost of Quality ("COQ") system is isolated from other KPI (Key Performance Indicators) systems, missing the opportunity for more in-depth understanding of cause-effect relationships for the Cost of Quality ("COQ") results.
For any measurement system, it should cost less than ~1% of the savings generated by the use of the measurement.
Things to Consider Before Implementing Cost of Quality ("COQ") 1. Is the management team committed to making rapid changes for maximum profitability, within the imposed constraints (eg. Company's Mission, laws & regulations, stakeholder satisfaction, etc.)?
2. Are there "sacred cows", legacy systems, departmental silos, and empire building that are exempt from re-evaluation?
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3. Are the hard costs (payroll, raw materials, utilities, etc.) more easily measured (or more important) than the soft costs (morale, employee satisfaction, market share, plant capacity utilization, customer's losses, supplier's losses, societal losses)?
4. Are the current management measurement systems (eg. KPI's, scrap, rework, excess freight charges, stock outages, absenteeism, productivity, profitability, etc.) Compatible with Cost of Quality ("COQ")? Can these other systems be adapted to include Cost of Quality ("COQ") without neither duplication nor conflict?
5. Will people be receiving mixed messages and conflicting signals between Cost of Quality ("COQ") and the traditional management measurements?
6. Is there management commitment to do something about the Cost of Quality ("COQ") data on a timely basis?
7. Is there COQ Software available that suits your current and future needs for maximum value from data at minimum cost? 8. If analysis of the control chart indicates that the process is currently under control (i.e. is stable, with variation only coming from sources common to the process) then data from the process can be used to predict the future performance of the process. If the chart indicates that the process being monitored is not in control, analysis of the chart can help determine the sources of variation, which can then be eliminated to bring the process back into control. A control chart is a specific kind of run chart that allows significant change to be differentiated from the natural variability of the process. 9. The control chart can be seen as part of an objective and disciplined approach that enables correct decisions regarding control of the process, including whether or not to change process control parameters. Process parameters should never be adjusted for a process that is in control, as this will result in degraded process performance 10. If analysis of the control chart indicates that the process is currently under control (i.e. is stable, with variation only coming from sources common to the process) then data from the process can be used to predict the future performance of the process. If the chart
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indicates that the process being monitored is not in control, analysis of the chart can help determine the sources of variation, which can then be eliminated to bring the process back into control. A control chart is a specific kind of run chart that allows significant change to be differentiated from the natural variability of the process. 11. The control chart can be seen as part of an objective and disciplined approach that enables correct decisions regarding control of the process, including whether or not to change process control parameters. Process parameters should never be adjusted for a process that is in control, as this will result in degraded process performance
Quality management: - It is a method for ensuring that all the activities necessary to design, develop and implement a product or service are effective and efficient with respect to the system and its performance. Quality management can be considered to have three main components:1. Quality control 2. Quality assurance 3. Quality improvement. 4. Quality management is focused not only on product quality, but also the means to achieve it. Quality management therefore uses quality assurance and control of processes as well as products to achieve more consistent quality. Quality Management is all activities of the overall management function that determine the quality policy, objectives and responsibilities and implement them by means such as quality control and quality improvements within a quality system. 5. Quality management is not a recent phenomenon. Advanced civilizations that supported the arts and crafts allowed clients to choose goods meeting higher quality standards than normal goods. In societies where art and craft (and craftsmanship) were valued, one of the responsibilities of a master craftsman (and similarly for artists) was to lead their studio, train and supervise the work of their craftsmen and apprentices. The master craftsman set standards, reviewed the work of others and ordered rework and revision as necessary. One of the limitations of the craft approach was that relatively few goods could be produced; on the other hand an advantage was that each item produced could be individually shaped to suit the client.
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This craft-based approach to quality and the practices used were major inputs when quality management was created as a management science. 6. During the industrial revolution, the importance of craftsmen was diminished as mass production and repetitive work practices were instituted. The aim was to produce large numbers of the same goods. The first proponent in the US for this approach was Eli Whitney who proposed (interchangeable) parts manufacture for muskets, hence producing the identical components and creating a musket assembly line. The next step forward was promoted by several people including Frederick Winslow Taylor a mechanical engineer who sought to improve industrial efficiency. He is sometimes called "the father of scientific management." He was one of the intellectual leaders of the Efficiency Movement and part of his approach laid a further foundation for quality management, including aspects like standardization and adopting improved practices. Henry Ford also was important in bringing process and quality management practices into operation in his assembly lines. In Germany, Karl Friedrich Benz, often called the inventor of the motor car, was pursuing similar assembly and production practices, although real mass production was properly initiated in Volkswagen after world war two. From this period onwards, North American companies focused predominantly upon production against lower cost with increased efficiency. 7. Walter A. Shewhart made a major step in the evolution towards quality management by creating a method for quality control for production, using statistical methods, first proposed in 1924. This became the foundation for his ongoing work on statistical quality control. W. Edwards Deming later applied statistical process control methods in the United States during World War II, thereby successfully improving quality in the manufacture of munitions and other strategically important products. 8. Quality leadership from a national perspective has changed over the past five to six decades. After the Second World War, Japan decided to make quality improvement a national imperative as part of rebuilding their economy, and sought the help of Shewhart, Deming and Juran, amongst others. W. Edwards Deming championed Shewhart's ideas in Japan from 1950 onwards. He is probably best known for his management philosophy establishing quality, productivity, and competitive position. 9. In the 1950s and 1960s, Japanese goods were synonymous with cheapness and low quality (Just as Chinese goods are today), but over time their quality initiatives began to be successful,
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with Japan achieving very high levels of quality in products from the 1970s onward. For example, Japanese cars regularly top the J.D. Power customer satisfaction ratings. In the 1980s Deming was asked by Ford Motor Company to start a quality initiative after they realized that they were falling behind Japanese manufacturers. A number of highly successful quality initiatives have been invented by the Japanese for example: - Taguchi, QFD, Toyota Production System. Many of the methods not only provide techniques but also have associated quality culture aspects (i.e. people factors). These methods are now adopted by the same western countries that decades earlier derided Japanese methods. 10. Customers recognize that quality is an important attribute in products and services. Suppliers recognize that quality can be an important differentiator between their own offerings and those of competitors (quality differentiation is also called the quality gap). In the past two decades this quality gap has been greatly reduced between competitive products and services. This is partly due to the contracting (also called outsourcing) of manufacture to countries like India and China, as well internationalization of trade and competition. These countries amongst many others have raised their own standards of quality in order to meet International standards and customer demands. The ISO 9000 series of standards are probably the best known International standards for quality management. 11. The International Organization for Standardization (ISO) created the Quality Management System (QMS) standards in 1987. These were the ISO 9000, ISO 9001, ISO 9002 and ISO 9003which all were 1987 series of standards comprising which were applicable in different types of industries, based on the type of activity or process: designing, production or service delivery. The standards have been regularly reviewed every few years by the International Organization for Standardization. The version in 1994 and was called the ISO 9000:1994 series; comprising of the ISO 9001, 9002 and 9003. The last revision was in the year 2000 and the series was called ISO 9000:2000 series. However the ISO 9002 and 9003 standards were integrated and one single certifiable standard was created under ISO 9001:2000. Since December 2003, ISO 9002 and 9003 standards are not valid, and the organizations previously holding these standards need to do a transition from the old to the new standards. The ISO 9004:2000 document gives guidelines for performance improvement over and above the basic standard (i.e. ISO 9001:2000). This standard provides a measurement framework for improved
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quality management, similar to and based upon the measurement framework for process assessment. 12. The Quality Management System standards created by ISO are meant to certify the processes and the system of an organization and not the product or service itself. ISO 9000 standards do not certify the quality of the product or service. 13. Recently the International Organisation for Standardisation released a new standard, ISO 22000, meant for the food industry. This standard covers the values and principles of ISO 9000 and the HACCP standards. It gives one single integrated standard for the food industry and is expected to become more popular in the coming years in such industry. 14. ISO has a number of standards that support quality management, one group describes processes (including ISO 12207, ISO 15288) and another describes process assessment and improvement ISO 15504. The Software Engineering Institute has its own process assessment and improvement methods, called CMMi (Capability Maturity Model - integrated) and IDEAL respectively. 15. COST OF POOR QUALITY (COPQ): Cost of poor quality (COPQ) or poor quality costs (PQC) are defined as costs that would disappear if systems, processes, and products were perfect. COPQ was popularized by IBM quality expert H. James Harrington in his 1987 book Poor Quality Costs. COPQ is a refinement of the concept of quality costs. In the 1960s, IBM undertook an effort to study its own quality costs and tailored the concept for its own use. While Feigenbaum's term "quality costs" is technically accurate, it's easy for the uninitiated to jump to the conclusion that better quality products cost more to produce. Harrington adopted the name "poor quality costs" to emphasize the belief that investment in detection and prevention of product failures is more than offset by the savings in reductions in product failures.
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Conventional wisdom would tell us that when you have some costs you can directly control (Appraisal Costs) and others that you cannot (Failure Costs), that you should keep a tight reign on the controllable costs and hope for the best with the others. Like most paragraphs that begin with a statement about conventional wisdom, this one argues against that strategy. The fact is that you can exercise indirect control over your organizations Failure Costs by appropriately managing the Appraisal Costs. This is not to say that you should allow your Appraisal Costs to run wild. But it also infers that you may not want to cut them too deeply. All of your Failure costs (every dollar of them) are caused by a finite number of defects in your software. Every defect that you can remove more economically than you currently do represents money on your companys bottom line. Every defect you can remove in a more timely way represents hours or days (or weeks!) of schedule saved. Every defect that you avoid shipping to you customer, and every useful feature that you do ship is priceless good will that builds your reputation in the marketplace. The key is to find more efficient methods to detect and remove defects.
This is a list of the various methods that different organizations use to remove defects from their software. They are listed roughly in order from most effective to least effective (in terms of both time and cost per defect removed). Beside each is the word Appraisal or Failure, indicating how most of the effort involved in that activity would be classified.
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Activity
Cost of Effectivenes
Personal Reviews (PSP reviews) Software Inspections (Fagan Peer Reviews Compiling Unit Testing Beta Testing System Testing (and performance & Acceptance Testing Walkthroughs
Testing is a relatively ineffective way to remove defects, but it is still a necessary part of your development lifecycle. Rather than continuing to make it your main defect removal mechanism, you would do better to use it to gage of the effectiveness of your earlier defect removal activities like reviews, inspections and unit testing.
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The most costly condition occurs when a customer finds defects. Had the manufacturer or service organization found the defects, through much inspection, testing and checking, a less costly condition would have resulted. If the manufacturing or service organizations quality program had been geared toward defect prevention and continuous quality improvement, defects and their resulting costs would have been minimized, which is, obviously, the most desirable condition. The most costly condition occurs when a customer finds defects. Had the manufacturer or service organization found the defects, through much inspection, testing, and checking, a less costly condition would have resulted? If the manufacturing or service organization's quality program had been geared toward defect prevention and continuous quality improvement, defects and their resulting costs would have been minimizedobviously, the most desirable condition.
Recent successes have resulted in revisions to the classic model of optimum quality costs. Previously, prevention and appraisal costs were portrayed as rising asymptotically as defectfree levels were achieved there is increasing evidence that the processes of improvement and new loss prevention are themselves subject to increasing cost effectiveness. New technology has reduced inherent failure rates of materials and products, while robotics and other forms of automation have reduced human error during production, and automated inspection and testing have reduced the human error of appraisal. These developments have resulted in an ability to achieve perfection at finite costs.
The goal of any quality cost system, therefore, is to facilitate quality improvement effort that will lead to operating cost reduction opportunities.
Take direct attack on failure costs in an attempt to drive them to zero; Invest in the right prevention activities to bring about improvement;
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Reduce appraisal costs according to results achieved; and (4) continuously evaluate and redirect prevention efforts to gain further improvement. This strategy is based on the premise that For each failure there is a root cause Causes are preventable Prevention is always cheaper
In a practical sense, real quality costs can be measured and then reduced through the proper analysis of cause and effect. As failures are revealed through appraisal actions or customer complaints, they are examined for root causes and eliminated through corrective action. Elimination of root causes means p e r m a n e n t removal. The further along in the operating process that a failure is discoveredthat is, the nearer to product or service use by the customerthe more expensive it is to correct.
Usually, as failure costs are reduced, appraisal efforts can also be reduced in a statistically sound manner. The knowledge gained from this improvement can then be applied, through prevention activities or disciplines, to all new work. As straightforward as this approach may appear, it cannot work unless there is first a basic quality measurement system that clearly identifies the correctable elements of performance failures which represent the best potential for cost improvement. Such a system is designed to use the data from inspections, tests, process control measurements or evaluations, quality audits, and customer complaints as a measure of company performance and a source of determining cost reduction projects. This measurement is a basic and important part of
quality management. The potential for improvement can be determined by a system of accurate and dependable quality cost measurement and analysis.
Since every dollar of quality cost saved can have a positive effect on profits, the value of clearly identifying and using quality costs should be obvious. By minimizing quality costs, quality performance levels can be improved.
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Swaraj Division Plant 2 Chappercheri , Chandigarh Group of Colleges, Landran, Mohali, Punjab.
Farm Equipment Sector (FES) is a part of US $6.3 billion Mahindra group, which is amongst the top 10 industrial houses in India. The group has a leading presence in key sectors of the Indian economy, including the financial services, trade, retail and logistics, automotive components, after-market, information technology and infrastructure development.
The Mahindra group's Farm Equipment Sector (FES) is amongst the top three tractor brands in the world. It has won the Japan Quality Medal in 2007. It also holds the distinction of being the first tractor company globally to win the Deming Application Prize in 2003. FES is the first tractor company worldwide to win these honors. This shows the strong focus of FES on Quality and Customer Satisfaction. Today, the domestic market share of FES is around 42%. (Mahindra brand: 30% and Swaraj brand: 12%).
FES has 6 state-of-the-art manufacturing plants (including 2 plants of Swaraj) in India, 2 plants in China, 3 assembly plants in USA and 1 assembly plant in Australia. FES has its presence in around 25 countries across six continents with more than 1000 dealers world-wide. FES has a subsidiary agricultural tractor manufacturing company in India known as Mahindra Gujarat Tractor Limited (MGTL). FES has a Sustainability Committee in place to take care of the implementation of GRI requirements.
Some facts about the company: Industry Revenue Net income Automotive Farm Equipment 31,568.54 crore (US$ 6.85 billion) (2010). 2,871.49 crore (US$ 623.11 million) (2010).
Employees 16,000
MAHINDRA SWARAJ: Swaraj Group, part of Mahindra & Mahindra (FES Sector) is a dynamic and growing group, wherein focus is laid on generating economic prosperity for stakeholders, while growing harmoniously with the community and environment. Swaraj is one of the leading tractor manufacturers in India and the company is totally indigenous. Nearly 6, 00,000 Swaraj tractors operate in the field providing durable delight to the discerning farming community of India. Swaraj has over 600 dealers across the country. Swaraj Group has achieved
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ISO 14001:2004 & OHSAS 18001:2007 Certification and TS 16949 certification for Swaraj Automotives Ltd.
MANUFACTURING AND QUALITY CHECK PROCESS There are manufacturing shops like welding, assembly, paint shop, etc. 1. LMS (light machine shop): gears 2. HMS (Heavy Machine Shop): differential housing, gear box housing. 3. Assembly Shop 4. Paint Shop
There is buyout components quality check. Too many vendors are there. Standard Vendors are not checked. When everyday all shops start working, first testing is done at that point. Secondly when lots of material is there for example 40 gears are there in a lot, then 1-2 gears are picked at random and are tested. Third stage of testing is testing of finished product in stages eg. the car is tested on conveyor belt system.
At the Swaraj Division, 6 Quality posts were there out of which quality post QP- 4,5and 6 are merged. Finally there is final advice and touch up area. This is basically the rework area. QP1QP4: testing of the various parts of the product is done to test whether there is any defect or not. Travel Card is used for this evaluation process. There is a quality check team in every shop which consists of around 3-4 Diploma Engineer Trainee. Rework done is categorized as major rework, i.e. checking the noise in the differential, etc and minor rework includes repainting, etc. Training of the employees is basically done through session videos.
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Roller Testing: In this car is basically at one position and it is made to move in order to check the hydraulics, idle engine RPM, dent, left out paint area, etc. Road Test: In this testing the overall product is checked for tyre alignment, engine working, etc. Then there is Pre- Dispatch Inspection (PDI): Gate checking to check that the material that is being dispatched is in proper condition. Two copies of PDI report is there, one for the owner and the other for the dealer.
Quality Costing: Prevention cost Quality training Reliability engineering Pilot studies System Development Total Prevention Cost Appraisal Costs Material Inspection Supplies Inspection Reliability Testing Total Appraisal Cost Internal failure Costs Scrap Repair Rework Downtime Total Internal Costs External Failure Costs Off warranty repairs and replacements Customer Complaints 560000 8.21 865000 765000 980000 290000 2900000 12.68 11.17 14.36 4.25 42.75 Quarterly Cost (Rs.) 90000 400000 145000 200000 835000 Percentage Total (%) 1.32 5.86 2.12 2.93 12.24
500000
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7.33
Product Liability Transportation Losses Total External Failure Total Quality Costs Kaizen costing Poka yoke: full proof Quality Circle IQS( Initial Quality Service)
The Swaraj Division has a capacity of 1 lac units. However currently it is producing 60,000 tractors. There are seven different models of tractors that are designed and manufactured in this unit. Harvesters, combines and forklifts are also manufactured in this division. Units of harvesters manufactured 500 pa and forklifts produced are 1000 per annum.
Person Contacted: Ravinder Assistant Manager, M & M Ltd Swaraj Division. Phone +91-172-2273404
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Quality: The Companys quality department ensures that these processes support standard in the procurement of raw material, error profiling and proofing, best methods for checking product defects and regular quality audits.
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COST OF QUALITY MEASUREMENT For the year 2009-10 COST OF QUALITY INTERNAL QUALITY COST Costs related to scrap Rework Cost Invisible waste unused Special Tests (Problem examination) Product waste and reprocess Salaries of quality department Total Internal Cost EXTERNAL QUALITY COST Product Insurance premiums Total External Cost PREVENTION COST & APPRAISAL COST Quality System Audit Cost Training cost Repair Maintenance cost (of plant) Costs of special audit Total Prevention Cost Total cost of quality Production Value % of Production Value Person contacted: Mr. R.C Sharma Senior Manager (Finance) 1.2 cr 1.2 cr (Rs.) p.a.
1,00,000 6,00,000 2,30,000 35000000 600000 3.654 cr 6.325 cr (approx) 180 cr 3.51 %
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SIGMA FREUDENBERG NOK PVT. LTD. (An Indo German Japanese Joint Venture) - Established in 1964 World leader in sealing technology TS-16949, ISO-14001, OHSAS-18001 & ISO-9001 Certified Company
About The Company: In August' 2000 Delhi based Sigma Corporation, Freudenberg Germany & NOK Japan formed a joint venture company, Sigma Freudenberg NOK Pvt. Ltd. (SFN) to manufacture the Freudenberg & NOK range of seals in India and to act as a sole marketing arm of both partners for their products manufactured worldwide in India. This joint venture in India is closing one of the last gaps in the international set up of the Freudenberg NOK Group of Companies, since it is the 28th country and the 46th factory to manufacture the sealing range of their products. Being the unchallenged market leader in sealing technology, the Freudenberg & NOK, group of companies together with their Indian partner, Sigma will bring the latest technology in design, material, application engineering and production to India to support their Indian customers with state of the art seals, giving them a competitive edge in a more and more competitive environment. Freudenberg & NOK will support the company with all know how available and guarantee the implementation with a full time Technical Director from Germany, having more than 30 years experience in other group companies worldwide. The core team of the factory has been trained in Germany for 6 months and the sales engineers have been intensively trained by experienced design Engineers from Freudenberg & NOK. Production started in November 2001 and will continue to increase over the next years. Together with the trading business, Sigma Freudenberg NOK (SFN) will be able to offer a unique range of seals for every kind of application in the Engineering Industry. Access to all R&D centres within the group leads to the best and most economical solutions for the Indian customers. The involvement of Sigma Freudenberg NOK from the first design step onwards gives the customer, access to the worldwide knowhow of the Freudenberg & NOK group, whereas the management expertise of the Sigma Group ensures the best possible implementation of the Freudenberg & NOK know how and technology in the Indian Company.
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Sigma Freudenberg NOK is actively participating globally to continuously improve its performance in all business areas by adopting "GROWTTH" as its key strategy. Our success, along with ongoing organization streamlining and continuous improvement measures, are powerful indicators of our ability to meet the challenges of the market with close customer focus.
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Cost Of Quality(Rs.) JUNE 2010 Internal Quality Cost Costs related to scrap Rework Cost Unplanned sorting inspection Repeat inspections and tests Waste Discrepancies in quantities (Inventory Correction) Special Tests (Problem examination) Costs resulting from customer complaints which will not be compensated, e.g. costs of travelling, special examination, sorting tests, non-chargeable stoppage, etc. Costs resulting from extra transport under responsibility of FDS Salary of Q.A. Dept. Total Internal Cost External Quality Cost Scrapping of returned goods Rework of returned goods Costs of inspection and testing, rework, assembly and disassembly at the customers end Recall from field Chargeable subsequent expenditures at the customers, e.g. after process interruption Costs of warranty claims less insurance payments, if applicable Travel expenses and expense allowances Costs of special inspection and testing Product liability insurance premiums Total External Cost
3,00,000 27,33,713
20,000 20,000
Prevention Cost and appraisal cost Quality System Audit Cost Calibration Cost Supplier Development Cost Total Prevention Cost Production Value % of Production Value
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Clients: ABB Harig Rane TRW ABI Showa Tech Hindustan Hydraulics Simpsons Ashok Leyland Int. Combuston UT Bosch Knorr Voltas BHEL Komatzu Vickers Bajaj Tempo L & T Veljan Brakes India LML Wipro Delphi Automotive Systems Lincon Hellious Dantal Mahindra & Mahindra Eicher New Holland Escorts Oscar Hegglunds Royal Enfield
Contact at: Head Off. & Plant B-70, Industrial Area, Phase-VII, Sector-73, Mohali-160055(India)
Contact person: Mr. Anil Gupta (Senior Manager Finance & Accounts) Mr. Rajesh Garg (Head QA - dept)
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Manufacturing excellence This feat is entirely based on the company's constant endeavour to meet aspirations of a large and diverse demography, by providing the best through innovative products and services. Today, each car from the Maruti Suzuki factories at Gurgaon, and Manesar, Haryana, North India are the tangible evidence of Quality, manufacturing standards and efficiency. Lean manufacturing Maruti Production System or MPS draws learning's from its parent company Suzuki Motor Corporation's concepts on `lean manufacturing' under Suzuki Production System i.e. SPS. Setting trends in new products and achieving customer delight starts with Manufacturing Excellence and Maruti's manufacturing excellence hinges around four important pillars-Cost, Quality, Safety and Productivity. Cost Every employee working on the line is 'cost sensitive' and functions in capacity of a Cost Manager. He is a key contributor in suggesting how to keep costs of production under control. Quality A product of poor quality requires repeated inspections, entails wastage in terms of repairs and replacements. "Do it right first time", is the principle followed to avoid wastage. To ensure quality, robots were devices and deployed especially where they reduced worker fatigue and were critical in delivering consistent quality. With consistent improvements in the plant the company was able to manufacture over 600,000 vehicles in 2006-07 with an installed capacity of just 350,000 vehicles per year.
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COST OF QUALITY Prevention cost Quality training Reliability engineering Pilot studies System Development Total Prevention Cost Appraisal Costs Material Inspection Supplies Inspection Reliability Testing Total Appraisal Cost Internal failure Costs Scrap Repair Rework Special Tests (Problem examination) Costs resulting from customer complaints which will not be compensated, e.g. costs of travelling, special examination, sorting tests, non-chargeable stoppage, etc. Total Internal Costs External Failure Costs Off warranty repairs and replacements Customer Complaints Product Liability Total External Failure Total Quality Costs 1520000 9.63 1000000 1140000 1560000 1310000 1110000 6.34 7.22 9.88 8.3 7.03 Cost per annum(Rs.) 240000 1200000 600000 960000 3000000 Percentage Total (%) 1.52 7.60 3.80 6.08 19.01
6120000
38.78
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Regd. Office: SCO 99-100, 3rd & 4th Floor, Sector 17-B, Chandigarh-160017(India) Ph. : +91-172-3914646, 3914647 Fax: +91-172-3914645 Works: Village Sundhran, P.O. Mubarakpur, Derabassi(Pb.) 45, Industrial Area, Phase II, Panchkula. Website: www.parabolicdrugs.com
About the Company: Parabolic Drugs Limited is one of the fast growing API (Active Pharmaceutical Ingredients) and API intermediate manufacturing and marketing company in with increasing international presence and a strong R&D foundation, based at Chandigarh, India. Commissioned in 1998, PDL has two fully functional, state of the art manufacturing units, a WHO-GMP certified Unit based in Derabassi (Punjab) and a world class Semi Synthetic Penicillin manufacturing plant at Panchkula, (Haryana) with one of its products been approved for sales to USA, respectively. PDL has a dedicated Custom Synthesis and Research & development Centre at Barwala (Haryana), fully equipped with latest analytical facilities and backed up with GMP pilot plant for scale up of technologies and filing of DMFs. Over the last twelve years of its existence, PDLs management has created a scalable business model in the API & API Intermediate segment to offer a product basket of Semi Synthetic Penicillins (oral & Sterile) and Cephalosporins (oral) and Cephalosporin Sterile. The Companys foray into Custom Synthesis & Contract Manufacture for innovator companies in US and Europe began in 2009 and it has made sizable inroads in the segment, having successfully executed orders for US based counterparts and many custom synthesis projects in process. This phenomenal growth has been driven by a vision of INR 1000 Crores, Global API and CRAMS Company by the year 2011-2012 under the leadership of Mr. Pranav Gupta, a young and dynamic first generation entrepreneur. The Company came out with its initial Public Office and got listed at NSE & BSE w.e.f. July 1st, 2010. It has recorded a turnover of Rs 559 crores in FY 2009 10 with a CAGR of 60% over the last five years. The Company has set forth huge expansion plans, including inorganic growth. Parabolic Drugs Limited (PDL) received its certification of European Union in july 2010, for its Cephalasporin manufacturing facility in Derabassi, Punjab.The company has received approval
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for three of its molecules namely, Cefuroxime Axetil, Cefpodoxime Proxetil and Cefixime Trihydrate. This will enable the company to sell its products into Europe, Canada and Australian markets, thus giving a boost to Companys vision of building its business in regulated markets. With this EU-GMP certification of its Derabassi facility, PDL has expanded its sales reach in the highly regulated markets and has positioned itself as a strong API company. The company has a stronghold in antibiotic space and marking its presence in the Custom Synthesis and Contract manufacturing (CRAMS) segment. PRODUCTS: SSP(Semi Synthetic Penicillin) , CEPH(Cephalosporin), 6API Some basic facts about the company HQ Region Industry Type Founded Chandigarh Area, India Pharmaceuticals Public Company 1996
KEY FINANCIAL HIGHLIGHTS(FY-10) Gross Sales: Q4 FY10 up 35.90% to Rs. 183.78 Crores; FY10 up 30.10% to Rs.559.00 Crores
Launch of 5 new products in Cephalosporin antibiotic APIs, oral and sterile range Penetration of new geographies exports made to 45 countries in fiscal 2010 Net Profit: Q4 FY10 up 105.71% to Rs. 11.52 Crores; FY10 up 42.84% to Rs. 34.20 Crores. Key Highlights
Received Certificate of Suitability (COS) from the European Directorate for the Quality of Medicines (and Healthcare), France (EDQM) for its DMF filed for Cefuroxime Axetil Amorphous - granting permission to sell the product in the regulated markets of the European Union Executed 8 custom synthesis contracts for global innovator and biotech companies since January 2010 Signed long term sales contracts with Ranbaxy, Lindopharm Germany and Chemworth USA
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Commercial production at phase I of the Chachrauli facility for manufacturing nonantibiotic products to start in September 2010. Company has a pipeline of 20 nonantibiotic products Expect total capacity expansion of 80% in the next twelve months time.
QUALITY PROCESS OF API (ACTIVE PHARMACEUTICAL INGREDIENTS) BUSINESS 1. Incoming Quality Control: Raw materials are imported from China, Hong Kong, Taiwan and also domestically. First Quality Check when the vendors deliver the raw material. 2. Second testing : When the raw material is received at the plant. 3. Processing check: in conformance with the SOP(Standard Operating Procedure): whether the raw material that is received is actually the desired one or not. 4. Employees quality oriented training program: rigorous training of employees. 5. Quality Assurance: checking the product that is being delivered to external agencies after processing. 6. Cost incurred in terms of customer audit and accredit ion costs: the quality is maintained under various regulatory accreditions like WHOGMP(World Health Organization good manufacturing practice), EUGMP(European good manufacturing Practice) and ISO 14001: 2004
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COST OF QUALITY FOR YEAR 2009 Cost (in % of actual cost of quality) Appraisal Costs Testing cost Incoming Quality control cost Infrastructural quality standards Total Appraisal costs Prevention cost GMP training Employee Quality oriented training Research and development for quality enhancemeny Customer audits Quality audits Total Prevention costs Internal failure Costs Rework Total Internal Costs External Failure Costs Total Quality Costs Total Cost Cost of Quality as a Percentage of total cost 8% 10% 15% 33%
40 40 8 800
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