The document discusses VDA 6.3, a standard for quality management system audits. It describes the standard's focus on assessing process performance rather than just conformance. The VDA 6.3 audit analyzes processes to detect risks and weaknesses. It evaluates four key elements: process responsibility, target orientation, communication, and risk identification. The audit also assesses processes across the product lifecycle from project planning to after-sales service. Organizations are rated on a color-coded scale after the audit to indicate capabilities and needs for improvement.
The document provides an overview of a webinar presented by Omnex on VDA 6.3 Management. Omnex is an international consulting, training and software development organization that specializes in integrated management system solutions. The webinar covered VDA 6.3 process auditing standards including the audit process, product life cycle, and a review of sections P2 through P5 which relate to project management, planning product development, carrying out development, and supplier management.
VDA 6.3 Training Material From VDiversify.com | VDA 6.3 Process Audit Trainin...VDiversify
油
Note: Whoever is using this Training Material on their Website shall Link back to www.vdiversify.com as the Original Author...
VDA 6.3 full form stands for Verband Der Deutschen Automobilindustrie.
VDA 6.3 is one of the excellent tools for in-depth manufacturing process audits within the automotive industry which acts as a guideline for performing audits.
The VDA 6.3 is now considered to be one of the most preferred or used manufacturing process audit tool which helps you find all kinds of gaps throughout the organization, especially in manufacturing lines or production areas which helps to close the gaps with proper robust corrective actions.
This document provides an introduction to statistical process control (SPC). It discusses the limitations of inspection and why SPC is better. It explains that SPC allows monitoring of processes to detect changes before defective products are produced. Various control chart templates are shown and key SPC concepts are defined, including sources of variation, the central limit theorem, and using average and range to monitor process behavior over time. Examples are provided to illustrate variability, distributions, and how control charts can be used.
The document discusses guidelines for auditing serial production processes. It will first examine the requirements of the "Red Book" and give importance to key questions. Process risks will be identified using a "Turtle Diagram" tool. Additionally, commonly found risks revealed by the diagrams will be added to the auditor's list of open-ended questions. The document provides an overview of serial production audits but notes that full expertise requires authorized training and practice. It then outlines several questions for evaluating different aspects of the serial production process.
The document provides information about Production Part Approval Process (PPAP). It discusses what PPAP is, its purpose, when it is required, benefits of PPAP submissions, elements of a PPAP submission including a production warrant, submission levels, and definitions of risk. Key points covered are that PPAP is used to reduce risks prior to product release, it provides evidence that requirements are understood and the process is capable of production, and it manages change and ensures product conformance.
Advanced product quality planning (APQP) is a framework for developing new products with a focus on meeting customer requirements. It involves 5 phases - planning, product design, process design, validation, and feedback. Key aspects of APQP include establishing cross-functional teams, using tools like FMEAs to prevent issues, designing control plans and statistical process control methods, conducting validation trials, and promoting continuous improvement. APQP aims to standardize quality planning processes for increased collaboration with suppliers.
This document discusses process audits in the automobile industry. It highlights two important mindsets before an audit: having ownership over your business and knowing what you know as well as what you don't know. It then provides details on typical organization structures for audits and compares different types of audits. The rest of the document focuses on executing process audits according to the VDA6.3 standard, including checking previous reports, analyzing data and processes, developing a detailed audit plan, and conducting the on-site audit. Benefits of using the VDA6.3 standard are also listed, such as providing a measurable assessment and identifying key processes to reduce risks.
Six Sigma is a data-driven approach to process improvement that aims to reduce defects. It uses statistical methods and the DMAIC framework (Define, Measure, Analyze, Improve, Control) to identify and address root causes of defects. The document provides an overview of Six Sigma, including its goals of reducing costs and improving customer experience. It also describes the five steps of DMAIC and some of the tools used in each step, such as process mapping in Define and data collection/analysis in Measure and Analyze to identify problems and root causes.
The document discusses the Production Part Approval Process (PPAP), including when PPAP submissions are required, the different submission levels, and the forms and documents required for each submission level. A PPAP submission is needed for new parts, design or process changes, changes in suppliers, inactive tooling, and more. The default submission level is level 3, which requires samples, supporting data, a design record, a process flow diagram, and more. Level 1 requires only a warranty, while level 2 adds limited data and samples.
Gray areas of vda 6.3 process auditors Kiran Walimbe
油
The document discusses several topics that are often unclear or lack detailed coverage during VDA 6.3 process auditing training, including:
1. NTF guidelines and the NTF process for analyzing customer complaints and implementing corrective actions.
2. The trigger matrix from VDA volume 2 which outlines how to handle different types of changes to products or processes.
3. Ergonomic design of workstations and workplace layouts to reduce injury risk and adapt to employees' needs.
The document discusses five core quality tools: APQP (Advanced Product Quality Planning), FMEA (Failure Modes and Effects Analysis), PPAP (Production Part Approval Process), MSA (Measurement Systems Analysis), and SPC (Statistical Process Control). It provides a brief overview of each tool, noting that APQP is used to develop products that satisfy customers, FMEA ensures potential problems are considered, PPAP ensures products meet specifications, MSA assesses measurement systems, and SPC enables process control and improvement. The document emphasizes that these five tools are considered core tools for quality management.
Dear All, I have prepared this presentation to get a better understanding of Statistical Process Control (SPC). This is a very informative presentation and giving information about the History of SPC, the basics of SPC, the PDCA approach, the Benefits of SPC, application of 7-QC tools for problem-solving. You can follow this technique in your day to day business working to solve the problems. Thanking you.
The document discusses the changes being made to the ISO/TS 16949 standard for quality management systems in the automotive industry. The standard is being changed to IATF 16949 and will be based on and require compliance with ISO 9001:2015. Some key changes include a new high level structure for management systems, greater emphasis on risk-based thinking and process approach, more leadership requirements, and addressing risks and opportunities rather than just preventative actions. The transition to the new standard focuses on integrating quality management into business strategies and emphasizing top management's responsibility for continual improvement.
IATF 16949:2016 is an automotive quality management system standard that is based on ISO 9001:2015 with additional automotive industry requirements. It aims to prevent defects, reduce variation and waste, and promote continual improvement. The standard contains 10 clauses covering quality management principles, leadership involvement, risk-based planning, resource management, production control, performance evaluation, and continual improvement. Key aspects include supplier management, design and development processes, internal auditing, management reviews, and corrective and preventive action.
This document outlines the 8D problem solving process used by Ford Motor Company to continuously improve quality and prevent issues from reoccurring. The 8D process involves 8 disciplines: 1) Define the problem/failure, 2) Establish an interim containment action, 3) Determine the root cause(s), 4) Choose a permanent corrective action, 5) Implement and validate the corrective action, 6) Implement actions to prevent recurrence, 7) Recognize the problem-solving team, and 8) Document lessons learned. Each discipline involves defining objectives, collecting data, verifying solutions, and ensuring the problem is fully resolved before progressing to the next step. The goal is to take a structured, cross-functional team approach
Advanced Product Quality Planning (APQP) is a structured approach to product and process development that aims to ensure suppliers understand customer requirements and are able to meet them. It involves 5 phases - planning and defining the program, product design and development, process design and development, product and process validation, and feedback and assessment. The key goals of APQP are up-front quality planning, satisfying the customer, and supporting continual improvement. Common roadblocks to effective APQP implementation include a lack of management commitment, unclear responsibilities, and insufficient resources or knowledge.
The document discusses Advanced Product Quality Planning (APQP). It describes APQP as involving organizing a team, defining the scope, involving customers and suppliers, and using simultaneous engineering. The benefits of APQP are listed as directing resources to satisfy customers, promoting early identification of required changes, and avoiding late changes to promote a quality product on time at the lowest price. Key stages and inputs of the APQP process are also outlined.
Global Manager Group has prepared presentation to provide information regarding documentation requirements for revised IATF 16949:2016 Certification. It described all primary documents like manual, procedures, plans, audit checklist, etc in details.
For further information about IATF 16949:2016 documentation requirements visit @ https://www.globalmanagergroup.com/
This document outlines a measurement system analysis (MSA) project to evaluate a measurement gauge. It will:
1. Determine which measurement system and gauge will be studied according to the MSA plan and gauge repeatability and reproducibility analysis.
2. Establish test procedures in different departments to analyze the gauge's repeatability and reproducibility.
3. Determine the number of sample parts, repeated readings, and operators used in the study.
The document also provides background definitions and concepts for measurement system analysis, including accuracy, precision, bias, repeatability, reproducibility and their impacts on process variation. Sources of variation are identified.
The document discusses the differences between chronic and sporadic problems and the appropriate approaches to address each type. It defines chronic problems as existing for some time and requiring improvement projects to attain breakthroughs. Sporadic problems are deviations that require troubleshooting to restore normal performance. The document outlines the sequence for breakthrough analysis including diagnosis to find root causes and developing remedies. It also summarizes the key steps in troubleshooting sporadic problems and the link between root cause analysis and the management by fact approach.
The document provides guidance on developing an effective control plan with three key sections:
1. The administrative section identifies critical information about the part or process including part numbers, suppliers, and required approval signatures.
2. The main section defines the key process parameters and controls for each step, including specifications, measurement techniques, sample sizes, frequencies, control methods, and reaction plans.
3. Effective control plans also include audit plans as a separate line to regularly validate that the documented controls match actual practice and ensure continuous improvement.
What is MSA .
1. Why we Need MSA
2. How to use data.
3.Measurement Error Sources of Variation
Precision (Resolution, Repeat ability, Reproducibility)
Accuracy (Bias, Stability, Linearity)
4.What is Gage R&R?
5.Explain MSA Sheet
The document discusses measurement system analysis (MSA) which is used to evaluate measurement systems and understand sources of variation. Key points:
- MSA assesses measurement quality and identifies sources of error like bias, repeatability, reproducibility, stability, and linearity.
- It is required to make informed process adjustments and avoid wrong decisions from low quality measurement data.
- MSA studies involve multiple appraisers measuring multiple parts multiple times to calculate variation percentages.
- A sample MSA study shows data collection, calculations for repeatability, reproducibility, and overall variation to evaluate the measurement system.
How to solve problems (or at least try) with 8DStefan Kovacs
油
This document provides an overview of the 8D problem solving method. It begins with the goals of learning how to use 8D for problem solving. It then discusses the history and development of the 8D method at Ford Motor Company in the 1980s. The document also includes definitions of key terms used in 8D. It describes the typical steps and process flow for 8D problem solving. Finally, it provides details of an 8D procedure used at an X factory, outlining the initiation and requirements for conducting 8D analyses.
This document defines key concepts in measurement system analysis including accuracy, precision, stability, bias, repeatability, and reproducibility. It provides guidelines for conducting a measurement system analysis, including determining the number of appraisers and parts to measure, ensuring the measurement procedure is documented and followed, and analyzing the results in terms of stability, bias, and gauge R&R to determine if the measurement system is capable and can be used for decision making. The goal is to qualify measurement systems and identify opportunities for improvement.
This document discusses measurement system analysis (MSA), which is used to evaluate statistical properties of process measurement systems. MSA determines if current measurement systems provide representative, unbiased and minimal variability measurements. The document outlines the MSA process, including preparing for a study, evaluating stability, accuracy, precision, linearity, and repeatability and reproducibility. Accuracy looks at bias while precision considers repeatability and reproducibility. MSA is required for certification and helps identify process variation sources and minimize defects.
Six Sigma is a data-driven approach to process improvement that aims to reduce defects. It uses statistical methods and the DMAIC framework (Define, Measure, Analyze, Improve, Control) to identify and address root causes of defects. The document provides an overview of Six Sigma, including its goals of reducing costs and improving customer experience. It also describes the five steps of DMAIC and some of the tools used in each step, such as process mapping in Define and data collection/analysis in Measure and Analyze to identify problems and root causes.
The document discusses the Production Part Approval Process (PPAP), including when PPAP submissions are required, the different submission levels, and the forms and documents required for each submission level. A PPAP submission is needed for new parts, design or process changes, changes in suppliers, inactive tooling, and more. The default submission level is level 3, which requires samples, supporting data, a design record, a process flow diagram, and more. Level 1 requires only a warranty, while level 2 adds limited data and samples.
Gray areas of vda 6.3 process auditors Kiran Walimbe
油
The document discusses several topics that are often unclear or lack detailed coverage during VDA 6.3 process auditing training, including:
1. NTF guidelines and the NTF process for analyzing customer complaints and implementing corrective actions.
2. The trigger matrix from VDA volume 2 which outlines how to handle different types of changes to products or processes.
3. Ergonomic design of workstations and workplace layouts to reduce injury risk and adapt to employees' needs.
The document discusses five core quality tools: APQP (Advanced Product Quality Planning), FMEA (Failure Modes and Effects Analysis), PPAP (Production Part Approval Process), MSA (Measurement Systems Analysis), and SPC (Statistical Process Control). It provides a brief overview of each tool, noting that APQP is used to develop products that satisfy customers, FMEA ensures potential problems are considered, PPAP ensures products meet specifications, MSA assesses measurement systems, and SPC enables process control and improvement. The document emphasizes that these five tools are considered core tools for quality management.
Dear All, I have prepared this presentation to get a better understanding of Statistical Process Control (SPC). This is a very informative presentation and giving information about the History of SPC, the basics of SPC, the PDCA approach, the Benefits of SPC, application of 7-QC tools for problem-solving. You can follow this technique in your day to day business working to solve the problems. Thanking you.
The document discusses the changes being made to the ISO/TS 16949 standard for quality management systems in the automotive industry. The standard is being changed to IATF 16949 and will be based on and require compliance with ISO 9001:2015. Some key changes include a new high level structure for management systems, greater emphasis on risk-based thinking and process approach, more leadership requirements, and addressing risks and opportunities rather than just preventative actions. The transition to the new standard focuses on integrating quality management into business strategies and emphasizing top management's responsibility for continual improvement.
IATF 16949:2016 is an automotive quality management system standard that is based on ISO 9001:2015 with additional automotive industry requirements. It aims to prevent defects, reduce variation and waste, and promote continual improvement. The standard contains 10 clauses covering quality management principles, leadership involvement, risk-based planning, resource management, production control, performance evaluation, and continual improvement. Key aspects include supplier management, design and development processes, internal auditing, management reviews, and corrective and preventive action.
This document outlines the 8D problem solving process used by Ford Motor Company to continuously improve quality and prevent issues from reoccurring. The 8D process involves 8 disciplines: 1) Define the problem/failure, 2) Establish an interim containment action, 3) Determine the root cause(s), 4) Choose a permanent corrective action, 5) Implement and validate the corrective action, 6) Implement actions to prevent recurrence, 7) Recognize the problem-solving team, and 8) Document lessons learned. Each discipline involves defining objectives, collecting data, verifying solutions, and ensuring the problem is fully resolved before progressing to the next step. The goal is to take a structured, cross-functional team approach
Advanced Product Quality Planning (APQP) is a structured approach to product and process development that aims to ensure suppliers understand customer requirements and are able to meet them. It involves 5 phases - planning and defining the program, product design and development, process design and development, product and process validation, and feedback and assessment. The key goals of APQP are up-front quality planning, satisfying the customer, and supporting continual improvement. Common roadblocks to effective APQP implementation include a lack of management commitment, unclear responsibilities, and insufficient resources or knowledge.
The document discusses Advanced Product Quality Planning (APQP). It describes APQP as involving organizing a team, defining the scope, involving customers and suppliers, and using simultaneous engineering. The benefits of APQP are listed as directing resources to satisfy customers, promoting early identification of required changes, and avoiding late changes to promote a quality product on time at the lowest price. Key stages and inputs of the APQP process are also outlined.
Global Manager Group has prepared presentation to provide information regarding documentation requirements for revised IATF 16949:2016 Certification. It described all primary documents like manual, procedures, plans, audit checklist, etc in details.
For further information about IATF 16949:2016 documentation requirements visit @ https://www.globalmanagergroup.com/
This document outlines a measurement system analysis (MSA) project to evaluate a measurement gauge. It will:
1. Determine which measurement system and gauge will be studied according to the MSA plan and gauge repeatability and reproducibility analysis.
2. Establish test procedures in different departments to analyze the gauge's repeatability and reproducibility.
3. Determine the number of sample parts, repeated readings, and operators used in the study.
The document also provides background definitions and concepts for measurement system analysis, including accuracy, precision, bias, repeatability, reproducibility and their impacts on process variation. Sources of variation are identified.
The document discusses the differences between chronic and sporadic problems and the appropriate approaches to address each type. It defines chronic problems as existing for some time and requiring improvement projects to attain breakthroughs. Sporadic problems are deviations that require troubleshooting to restore normal performance. The document outlines the sequence for breakthrough analysis including diagnosis to find root causes and developing remedies. It also summarizes the key steps in troubleshooting sporadic problems and the link between root cause analysis and the management by fact approach.
The document provides guidance on developing an effective control plan with three key sections:
1. The administrative section identifies critical information about the part or process including part numbers, suppliers, and required approval signatures.
2. The main section defines the key process parameters and controls for each step, including specifications, measurement techniques, sample sizes, frequencies, control methods, and reaction plans.
3. Effective control plans also include audit plans as a separate line to regularly validate that the documented controls match actual practice and ensure continuous improvement.
What is MSA .
1. Why we Need MSA
2. How to use data.
3.Measurement Error Sources of Variation
Precision (Resolution, Repeat ability, Reproducibility)
Accuracy (Bias, Stability, Linearity)
4.What is Gage R&R?
5.Explain MSA Sheet
The document discusses measurement system analysis (MSA) which is used to evaluate measurement systems and understand sources of variation. Key points:
- MSA assesses measurement quality and identifies sources of error like bias, repeatability, reproducibility, stability, and linearity.
- It is required to make informed process adjustments and avoid wrong decisions from low quality measurement data.
- MSA studies involve multiple appraisers measuring multiple parts multiple times to calculate variation percentages.
- A sample MSA study shows data collection, calculations for repeatability, reproducibility, and overall variation to evaluate the measurement system.
How to solve problems (or at least try) with 8DStefan Kovacs
油
This document provides an overview of the 8D problem solving method. It begins with the goals of learning how to use 8D for problem solving. It then discusses the history and development of the 8D method at Ford Motor Company in the 1980s. The document also includes definitions of key terms used in 8D. It describes the typical steps and process flow for 8D problem solving. Finally, it provides details of an 8D procedure used at an X factory, outlining the initiation and requirements for conducting 8D analyses.
This document defines key concepts in measurement system analysis including accuracy, precision, stability, bias, repeatability, and reproducibility. It provides guidelines for conducting a measurement system analysis, including determining the number of appraisers and parts to measure, ensuring the measurement procedure is documented and followed, and analyzing the results in terms of stability, bias, and gauge R&R to determine if the measurement system is capable and can be used for decision making. The goal is to qualify measurement systems and identify opportunities for improvement.
This document discusses measurement system analysis (MSA), which is used to evaluate statistical properties of process measurement systems. MSA determines if current measurement systems provide representative, unbiased and minimal variability measurements. The document outlines the MSA process, including preparing for a study, evaluating stability, accuracy, precision, linearity, and repeatability and reproducibility. Accuracy looks at bias while precision considers repeatability and reproducibility. MSA is required for certification and helps identify process variation sources and minimize defects.
The document discusses different static techniques used in software testing, including various types of reviews. It describes reviews as a way to uncover errors by presenting work to other parties. Various review types are covered, ranging from informal reviews with no process to more formal inspections with defined roles and processes. The key aspects and purposes of reviews, walkthroughs, technical reviews, and inspections are outlined.
Today it is crucial for organizations to pay even greater attention on quality management as the
importance of this function in achieving ultimate business objectives is increasingly becoming
clearer. Importance of the Quality Management (QM) Function in achieving basic need by
ensuring compliance with Capability Maturity Model Integrated (CMMI) / International
Organization for Standardization (ISO) is a basic demand from business nowadays. However,
QM Function and its processes need to be made much more mature to prevent delivery outages
and to achieve business excellence through their review and auditing capability. Many
organizations now face challenges in determining the maturity of the QM group along with the
service offered by them and the right way to elevate the maturity of the same. The objective of
this whitepaper is to propose a new model the Audit Maturity Model (AMM) which will
provide organizations with a measure of their maturity in quality management in the perspective
of auditing, along with recommendations for preventing delivery outage, and identifying risk to
achieve business excellence. This will enable organizations to assess QM maturity higher than
basic hygiene and will also help them to identify gaps and to take corrective actions for
achieving higher maturity levels. Hence the objective is to envisage a new auditing model as a
part of organisation quality management function which can be a guide for them to achieve
higher level of maturity and ultimately help to achieve delivery and business excellence.
The document discusses quality management in project management. It begins with introductions and outlines the course schedule which includes topics like quality management, risk management, procurement management, and communication management. It then provides definitions and explanations of quality management concepts like quality versus grade, quality assurance, quality control, prevention over inspection, continuous improvement using PDCA cycles, and more. Finally, it discusses the three quality management processes - plan quality management, perform quality assurance, and control quality.
Today it is crucial for organizations to pay even greater attention on quality management as the
importance of this function in achieving ultimate business objectives is increasingly becoming
clearer. Importance of the Quality Management (QM) Function in achieving basic need by
ensuring compliance with Capability Maturity Model Integrated (CMMI) / International
Organization for Standardization (ISO) is a basic demand from business nowadays. However,
QM Function and its processes need to be made much more mature to prevent delivery outages
and to achieve business excellence through their review and auditing capability. Many
organizations now face challenges in determining the maturity of the QM group along with the
service offered by them and the right way to elevate the maturity of the same. The objective of
this whitepaper is to propose a new model the Audit Maturity Model (AMM) which will
provide organizations with a measure of their maturity in quality management in the perspective
of auditing, along with recommendations for preventing delivery outage, and identifying risk to
achieve business excellence. This will enable organizations to assess QM maturity higher than
basic hygiene and will also help them to identify gaps and to take corrective actions for
achieving higher maturity levels. Hence the objective is to envisage a new auditing model as a
part of organisation quality management function which can be a guide for them to achieve
higher level of maturity and ultimately help to achieve delivery and business excellence.
This document provides an overview of Total Quality Management (TQM) concepts including definitions of quality, inspection, quality control, quality assurance, and quality management. It discusses quality gurus like Deming, Juran, Crosby, and Taguchi and some of their key philosophies and tools. Specifically, it covers Deming's PDCA cycle and 14 points, Juran's quality trilogy, Crosby's 14 points and concept of "quality is free", and Taguchi's concept of customer tolerance limits and quality loss function which quantifies costs of poor quality over the lifetime of a product.
The International Aerospace Quality Group (IAQG) expects to issue a revised version of the Aerospace Standard AS9101 later this year. The revision, called Rev E, will focus audits more on process effectiveness and the achievement of quality objectives. Auditors will intensely examine process management and will expect to see that quality performance is monitored and measured against objectives. Organizations need to select key performance indicators (KPIs) that reflect critical success factors and review them to ensure they still apply given changes to processes, objectives, or business scope. Rev E provides an opportunity for organizations to re-examine their quality policies and processes in preparation for the new audit standards.
Quality Introduction Quiz - Series 1 By Maya.johnsqms
油
The document is a quiz on quality management systems with answers provided. It covers:
- The year the first edition of ISO/TS 16949 was released (1999).
- The main reasons for implementing ISO/TS 16949 certification are to improve customer satisfaction, qualify for the automotive industry, and engage employees.
- DMAIC stands for Define, Measure, Analyze, Improve, Control and is a process improvement strategy.
- PDCA (Plan, Do, Check, Act) is a model for continuous improvement popularized by William Edwards Deming.
- Process capability index measures how well a process operates within specification limits.
- Clause 4 of ISO/TS defines
This document outlines the key elements of a quality management system, including a quality policy, quality objectives, quality manual, organizational structure, data management, purchasing processes, customer satisfaction, continuous improvement, quality instruments, and document control. The quality policy is a statement by top management regarding product quality expectations. Quality objectives define measurable goals for achieving the quality policy. The quality manual details how the quality management system operates. The organizational structure links quality responsibility to executive levels. Data management develops architectures and procedures for information lifecycles. Purchasing and other processes are also covered.
The document provides an overview of manual testing and the software development lifecycle. It defines key terms like software testing, verification and validation. It discusses different types of testing like static testing, white-box testing and black-box testing. It also explains software quality concepts like quality assurance and quality control. The document then introduces process standards like ISO and CMMI and maturity models. It describes various software development life cycle models like waterfall, prototyping and incremental development.
ISO tools _process_Capability
02:58
Online quiz (2)
惘忰惡悋 20210956. 惺惆 悒惘愕悋 悵悋 悋悵悴 愕 惘 悋悋 悋愕 惺悋 惡惘惆 悋悒惠惘.
愀惡
1.A register's functions include
(1 愀悸)
(a) Data storage
(b) Data movement
Neither (a) Not (b)
Both (a) And (b)
2.A flip-flop is presently in the SET state and must remain SET on the next clock pulse, What must J and K be?
(1 愀悸)
J=X , K=0
J=0 , K=1
J=1 , K=X
J=X , K=1
3.A 4-bit binary up/down counter is in the binary state of zero. What is the next state in the DOWN mode ?
(1 愀悸)
0001
1111
1000
1110
4.In SISO register if D0=1 , D1= 0 , D2= 0 , and D3=1.After three clock pulses, what are the data outputs?
(1 愀悸)
1001
0001
0110
1110
5.How many clock pulses are required to store data in PISO register
(1 愀悸)
One pulse
Two pulses
Three pulses
Four pulses
6.A 4 bit binary up/down counter is in the binary state of 1111. Whats is the next state in the UP mode ?
(1 愀悸)
1110
1111
0001
0000
7.A flip-flop is presently in the RESET state and must So to the SET state on the next clock pulse, What must J and K be?
(1 愀悸)
J=X , K=0
J=0 , K=1
J=1 , K=X
J=X , K=1
8.What is a group of flip-flops used for data storage called?
(1 愀悸)
Asynchronous counters
Synchronous counters
Registers
Non of the above
9.If the present state is 0111, the next state of a 4-bit up/down counter in the DOWN mode is 1000
(1 愀悸)
True
False
10.To enter a byte of data serially into an 8-bit shift register, there must be
(1 愀悸)
One clock pulse
Two clock pulses
Four clock pulses
Eight clock pulses
The document discusses the components of DMAIC, the methodology used in Six Sigma improvement projects. It begins by outlining some key requirements for Six Sigma projects, including leadership commitment, using facts to make decisions, and cross-functional team training. It then describes each stage of DMAIC - Define, Measure, Analyze, Improve, and Control - and lists some potential tools and activities used in each stage. The document concludes by listing several statistical tools that can be used throughout the Six Sigma improvement process.
This document provides a summary of Bhalchandra Rajadhyax's qualifications and experience in business process management, process consulting, and information security auditing. It includes:
- Over 17 years of experience in business process improvement, reengineering, program management, and performance improvement across various industries.
- Certifications in Six Sigma Black Belt, ISO management systems for quality, information security, environment, occupational health and safety, and more.
- Experience leading process improvement projects using techniques like Six Sigma, Lean, ISO standards, and developing quality management systems for various customers in retail, dairy, IT, and other industries.
- Conducting information security audits, developing audit tools and checklists,
This document provides an overview of quality concepts including definitions of quality, zero defects, customers, quality terms and concepts, inspection, sampling, and the differences between SPC and acceptance sampling. It defines quality as meeting customer expectations and conforming to specifications. Zero defects aims for no product or service defects. Customers are critical to quality and satisfaction. Total quality management, continuous improvement, six sigma, and PDCA model are quality approaches. Inspection and sampling are used to check for defects. SPC monitors processes while acceptance sampling accepts or rejects lots.
QMS Effectiveness: Tracking and Trending Quality Data - OMTEC 2017April Bright
油
What measurements are useful, and which metrics baseline makes sense to show the effectiveness of your quality management system? This presentation takes an ISO 13485 and 21 CFR, Part 820 approach to deciding what measurements are important, how trending makes an impact on risk-based decision-making, and why management review is just one of the ways to discuss and document your Quality Data activities.
This document provides an overview of quality principles and concepts. It defines key terms related to quality like defect, policy, procedure, process, and standard. It discusses different views of quality from the perspective of customers, producers, providers and suppliers. It also describes quality attributes for information systems and quality concepts like the PDCA cycle, cost of quality, six sigma quality, and the approaches of quality pioneers like Deming, Crosby and Juran.
The document discusses quality procedures and processes. It provides an overview of quality management systems and outlines some key aspects such as continual improvement, customer focus, leadership, and the importance of following documented procedures. Examples of quality procedures discussed include maintenance, product recalls, supplier assessment, and failure mode and effects analysis. Quality terminology is also defined.
4. Kiran Walimbe
The VDA recommends its members to apply VDA
6.3 (2010) standard for the implementation and
maintenance of Quality management System,
because it believes, higher expectations of
products require robust processes which must be
secure throughout the entire manufacturing and
supply chain.
While a System audit of TS 16949 or ISO 9001
seeks out the Conformance of the organization to
the written standards, the Process audit by VDA
6.3 way verifies the Performance of the
organization.
5. Kiran Walimbe
The processes get analyzed in such a way that
Risks and Weaknesses are detected in work-
processes and their interfaces. The auditor
ultimately is attempting to find out whether There is
a person responsible for the processes i.e. Process
Responsibility PR; Are the Processes directed
towards targets based upon the companies
requirements i.e. Target orientation TO; is
Important information (e.g. quality, problems)
communicated promptly & comprehensively to the
necessary persons i.e. Communication CO; and
are the Risks in the processes appropriately
identified & taken into account i.e. Risk
Identification RI.
6. Kiran Walimbe
PR, TO, CO and RI are the are general
requirements relating to a process (Process
Orientation) without which the operations &
effectiveness of the process in question cannot
be guaranteed and the customer interest might be
endangered.
These elements make up what is known as The
Generic Launch Pad.
Amongst other things, the VDA 6.3 process audit
ends up assessing the four elements of Generic
Launch Pad.
8. Kiran Walimbe
For auditing the Business Process one needs to
define a process; identify all the associated risks
and in the end evaluate the business process to
confirm adequate mitigation of all of these risks.
VDA 6.3 defines all business or service processes
though plotting of Turtle Diagrams. A typical
template is shown here.
The risks exist on the interfaces. The auditor first
generates a list of possible risks in this interface.
Then he makes up a list of Open Questions to seek
whether these risks really exists or not.
9. Kiran Walimbe
He goes to the work place, asks these questions,
gets the answers and comes back to convert these
open questions to closed questions. He now has
got Yes-No answers available to these questions.
With this set of derived closed questions he opens
his laptop, opens the authorized questionnaire
from VDA & records his findings.
The macros in the excel sheet do the rest of job. In
an answer sheet, he finds the detailed verdict. Not
only the averaged cumulative rating is there, but
also the systematic derivative in terms of Generic
Launch Pad (PR-TO-CO-RI) is available to guide us
on what needs to improve in our business set up.
11. Kiran Walimbe
VDA 6.3 breaks down a typical Product Life Cycle
into seven process elements calling them P1 to P7
as shown in diagram.
Out of these seven elements, the first one i.e.
Potential Analysis P1 applies only while assessing a
new and potential supplier.
The rest six elements get audited after confirming
award of contract & start of regular production.
12. Kiran Walimbe
The chart here shows the approximate starting
and closing points of these six phases in the entire
product life-cycle in manufacturing and supply
chain; which are:
P2-How well is the Project Managed
P3-APQP & Planning of Product & Process design
& development
P4-Product / Process realization or PPAP
P5-Effectiveness of Supplier management
P6-Process Analysis / Production (Most
elaborately done in VDA 6.3)
P7-After sales service, resolving customer related
issues & customer satisfaction
13. Kiran Walimbe
Classification Overall level of
achievement Eg
[%]
Description of the
classification
A Eg > or = 90 Quality capable
B 80 = or < Eg < 90 Conditionally
quality capable
C Eg < 80 Not quality
capable
At the end of this audit the audited organization may
get one of the following ratings.
14. Kiran Walimbe
Classification Yellow Red
Barred RED >14 One question
Controlled AMBER Max. 14 None
Released GREEN Max. 7 None
Special and different treatment to
evaluation of new suppliers.
The process audit for the process element P1,
occurs when a new supplier is identified to meet
some need of the organization. The audit Frame
work conditions are simple & consist of
Confidentiality agreement & Access permission,
the Timing is before the award decision and the
Risk analysis consists of Identifying product and
process risks. Simply put, Potential analysis is
nothing but Comparing the performance of similar
suppliers with that of the Potential Supplier.
15. Kiran Walimbe
P2 for Project Management:
There exists a comprehensive project management
(including quality planning & risk management) for
planning as well as for carrying out the process &
product development. The project organization is
equipped with the necessary resources, its tasks,
authority and expertise are defined and known. The
customer is informed of the project planning. A
change management (change control) (involving
the customer) is established.
16. Kiran Walimbe
P3 for Planning of project and Product design &
development:
The requirements necessary for the product &
process development are known. The feasibility of
the products & the processes to be developed is
assured. The product / process development plan
ensures that all essential activities are planned with
the customers agreement. This also includes the
need to take into account the necessary technical &
personnel resources. Supplier management take
into account all designated parts supplied.
17. Kiran Walimbe
P4 for realization of product / process development:
All defined tasks from the planning of the product
and process must be conducted in the realization
phase. Changes must be recognized & taken into
account in the planning. Reviews must be carried
out at specified intervals during the realization
phase. If target requirements are not achieved,
actions must be specified & monitored for
effectiveness.
18. Kiran Walimbe
P5 for Supplier Management:
Only approved / released & qualified suppliers are
used for serial production processes. Customer
requirements are known throughout the supply
chain and are implemented. Bought-in products
comply with the customer requirements which
have been agreed.
19. Kiran Walimbe
P6 for Process management / Production:
This is the element which is audited most
intensely. It is further divided into:
6.1 what goes into the process,
6.2 are all production processes controlled?
(Process sequence),
6.3 what functions support the process?
Personnel resources,
6.4 what facilities are used to achieve the
process? (Material resources),
6.5 How effectively is the process carried out?
(Effectiveness, efficiency, elimination of waste),
6.6 What should the process produce? (Process
result / output)
20. Kiran Walimbe
P7 for Customer service, Customer satisfaction and
Service:
The product as delivered meets the customers
requirements, Customer support and supply of
parts are ensured, There are effective and
sustainable failure elimination processes in place in
the event of complaints and rejects.
21. Kiran Walimbe
With this set of derived closed questions he opens
his laptop, opens the authorized questionnaire from
VDA & records his findings.
The macros in the excel sheet do the rest of job. In
an answer sheet, he finds the detailed verdict. Not
only the averaged cumulative rating is there, but
also the systematic conclusions in terms of Generic
Launch Pad (PR-TO-CO-RI) is available to guide us
on what needs to improve in our business set up.
22. Kiran Walimbe
In case of non-conformances, the ratings of
organization can go down. If it was earlier in A
category, it may get downgraded to either B or
worse to C. The remedial course open to the
organization consists of following steps:
Get its MR team trained in the ways of VDA 6.3
process auditing & commence in-house petrol
audits.
Find out where the ratings have suffered losses.
Take corrective actions & verify their
effectiveness thru the teams of senior
management.
Decide upon embracing Process Auditing, not to
please some external organizations but as means
of bringing home true and ever-lasting
improvements. After all it is great pride to build a
top performing organization & to work in it.
23. Kiran Walimbe
Those readers, who wish to get formally qualified in
auditing by VDA 6.3 (2010) process audit system,
can undertake following Training Programs
offered by UBF.B Management Pvt. Ltd.
Module A + B 2 ....................... Process Auditor
for Product Life Cycle (own company and suppliers)
Modules B 2............................ Process Auditor for
Product Life Cycle (own company and suppliers)
Module E (= Modules A + B 2+ C) Certified
Process Auditor for Product Life Cycle (any
company)
Ulrike Peper e-mail Q-training@ubfb.de or
e-Mail berlin@ubfb.de
I am available for your comments and queries on
kiran.walimbe@ubfb.de or kiranwalimbe@live.com