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Speaker Profile
WILLIAM LEVINSON

William A. Levinson, P.E., FASQ, CFPIM is the principal of Levinson Productivity Systems, P.C. He is an ASQ Certified Quality Engineer, Quality Auditor, Quality Manager, Reliability Engineer, and Six Sigma Black Belt, and the author of several books on quality, productivity, and management.


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$149.00
Use Cost of Quality Analysis to Improve the Bottom Line

 William Levinson
 August 05 2020
 01 : 00 PM EST    
 60 Minutes
 Download Catalog
Use Cost of Quality Analysis to Improve the Bottom Line

The coronavirus epidemic's disruption of complex international supply chains, along with threats by the Chinese government to intentionally disable U.S. supply chains by withholding vital inputs (references appear below), underscores the need to restore American manufacturing as rapidly as possible. Elimination of wastes including but not limited to the cost of poor quality will support and encourage reshor..

$149.00
How to Prepare for the HEROES Act’s Regulatory Standard for COVID-19 Prevention

 William Levinson
 September 14 2020
 03 : 00 PM EST    
 90 Minutes
 Download Catalog
How to Prepare for the HEROES Act’s Regulatory Standard for COVID-19 Prevention

The HEROES Act (Health and Economic Recovery Omnibus Emergency Solutions Act) requires, “Not later than 24 months after the date of enactment of this Act, the Secretary of Labor shall, pursuant to section 6 of the Occupational Safety and Health Act (29 U.S.C. 655), promulgate a final standard—(1) to protect employees” who are at occupational risk for exposure to SARS-CoV-2,” also known as COVID-19..

$149.00
Corrective and Preventive Action (CAPA) and Root Cause Analysis

 William Levinson
 October 01 2020
 01 : 00 PM EST    
 90 Minutes
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Corrective and Preventive Action (CAPA) and Root Cause Analysis

Corrective and preventive action (CAPA) is required by ISO 9001:2015, and is also common sense; we don't want to have to solve the same problem more than once. The automotive IATF 16949:2016 standard adds additional requirements for root cause analysis. Inadequate CAPA and/or root cause analysis are leading sources of ISO 9001 and IATF 16949 audit findings, and also FDA Form 483 citations. This comes as no ..

Showing 1 to 14 of 14 (1 Pages)
$150.00
BEST SELLER - Measurement Systems Analysis

 William Levinson
 Recorded Webinar
 60 Minutes
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BEST SELLER - Measurement Systems Analysis

This presentation will cover the fundamentals of measurement systems analysis (MSA), or gage reproducibility and repeatability, as required by ISO/TS 16949 and highly recommended otherwise. This includes the requirements in terms of parts and inspectors, as well as randomization of measurements, for a successful gage study as well as the mathematical calculations (which are in practice now handled by statis..

$150.00
BEST SELLER - Process Capability Analysis

 William Levinson
 Recorded Webinar
 60 Minutes
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BEST SELLER - Process Capability Analysis

Attendees will learn how to calculate process capability and process performance indices that are often required by internal or external customers of manufacturing processes. The webinar will show the relationship between a Six Sigma process and its performance index. The webinar will then go beyond this textbook material to cover processes that do not follow the normal (bell curve) distribution, and for wh..

$200.00
Introduction to Statistical Process Control

 William Levinson
 Recorded Webinar
 60 Minutes
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Introduction to Statistical Process Control

This webinar will introduce attendees to the foundations of statistical process control (SPC), including the effects of variation and accuracy on process quality. The definition of a Six Sigma process will be illustrated. Attendees will learn how to construct SPC charts that provide visual controls (easily understood signals) that tell production workers when the process requires adjustment to prevent the m..

$200.00
Measurement Systems Analysis

 William Levinson
 Recorded Webinar
 60 Minutes
 Refer a Friend
 Download Catalog
Measurement Systems Analysis

This presentation will cover the fundamentals of measurement systems analysis (MSA), or gage reproducibility and repeatability, as required by ISO/TS 16949 and highly recommended otherwise. This includes the requirements in terms of parts and inspectors, as well as randomization of measurements, for a successful gage study as well as the mathematical calculations (which are in practice now handled by statis..

$200.00
Process Capability Analysis

 William Levinson
 Recorded Webinar
 60 Minutes
 Refer a Friend
 Download Catalog
Process Capability Analysis

Attendees will learn how to calculate process capability and process performance indices that are often required by internal or external customers of manufacturing processes. The webinar will show the relationship between a Six Sigma process and its performance index. The webinar will then go beyond this textbook material to cover processes that do not follow the normal (bell curve) distribution, and for wh..

$200.00
What to Do When It's Not a Bell Curve

 William Levinson
 Recorded Webinar
 60 Minutes
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What to Do When It's Not a Bell Curve

Traditional statistical process control (SPC) and process capability assessment techniques assume that the critical to quality (CTQ) variable follows a normal (bell curve) distribution. This condition is fulfilled far more often in textbooks than in real factories, laboratories, and so on. If the statistical distribution is not a bell curve, estimates of the nonconforming fraction (defects per million oppor..

$200.00
Use Shingo Maps to Drive Continuous Improvement in ISO 9001:2015

 William Levinson
 Recorded Webinar
 60 Minutes
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Use Shingo Maps to Drive Continuous Improvement in ISO 9001:2015

This webinar will show how to expand Shingo maps from individual project applications into evolving, data-driven process documentation for an ISO 9001:2015 or related quality management system. Shingo maps support ISO 9001's process orientation, and also identify opportunities to reduce or eliminate wastes of time, material, and energy (muda). The latter applications support ISO 14001 and ISO 50001 as well ..

$200.00
Acceptance Sampling for Variables: ANSI/ASQ Z1.9

 William Levinson
 Recorded Webinar
 60 Minutes
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Acceptance Sampling for Variables: ANSI/ASQ Z1.9

This webinar will show how to use ANSI/ASQ Z1.9 (formerly MIL-STD 414) to define sampling plans for products with continuous-scale (variables) data, and use the accompanying switching rules to move between normal, reduced, and tightened inspection as required by the publication.ANSI/ASQ Z1.9 (formerly MIL-STD 414) is a widely accepted standard for sampling by variables (continuous scale measurements). The s..

$150.00
BEST SELLER - Acceptance Sampling for Variables: ANSI/ASQ Z1.9

 William Levinson
 Recorded Webinar
 60 Minutes
 Refer a Friend
 Download Catalog
BEST SELLER - Acceptance Sampling for Variables: ANSI/ASQ Z1.9

This webinar will show how to use ANSI/ASQ Z1.9 (formerly MIL-STD 414) to define sampling plans for products with continuous-scale (variables) data, and use the accompanying switching rules to move between normal, reduced, and tightened inspection as required by the publication.ANSI/ASQ Z1.9 (formerly MIL-STD 414) is a widely accepted standard for sampling by variables (continuous scale measurements). The s..

$200.00
The Dynamic Control Plan

 William Levinson
 Recorded Webinar
 60 Minutes
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The Dynamic Control Plan

Failure mode effects analysis (FMEA) and the control plan are both parts of advanced quality planning (AQP). FMEA, in fact, defines the control points or critical nodes of the control plan; process activities that must be controlled to ensure conformance of the critical to quality (CTQ) product characteristics. The dynamic control plan is a natural combination of the process FMEA and control plan into a sin..

$200.00
Process Failure Mode Effects Analysis and Control Plan

 William Levinson
 Recorded Webinar
 90 Minutes
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Process Failure Mode Effects Analysis and Control Plan

The control plan that is required in automotive applications (APQP) can be appended to the PFMEA to create a dynamic control plan. The control the plan is, in fact, synergistic with identification of the process and product characteristics and the preventive and detection controls cited in the PFMEA.Learning ObjectivesKnow the role of PFMEA in advanced quality planning (AQP) Know the role of PFMEA i..

Showing 1 to 14 of 14 (1 Pages)