Image
image
image
image


Other Section and Quality Organization Articles 'n News:
ASQ Sister Sections and other quality-focused organizations are requested and encouraged to forward your newsletters or articles for publication to: asqcincinnati@gmail.com

 


 


Innovations in Healthcare Delivery Conference
September 18 and 19
Medical Education and Research Center, Cincinnati Children's Hospital Medical Center





The Innovations in Healthcare Delivery conference series brings together healthcare managers, physicians, and researchers from a variety of backgrounds and specialties to present and discuss new insights and creative solutions for the efficient delivery of high-quality care.  The conference focus is 'Improving Patient Care by Rethinking Processes, Systems and Organizations'.  See the conference flyer for more details.

For more information on registration, lodging, speakers, and abstracts:  www.cincinnatichildrens.org/ihd-conference


 

Ohio Partnership for ExcellenceOhio Partnership for Excellence - Quest for Success Conference
September 22-23
Columbus Airport Marriott - Columbus, OH





The Ohio Partnership for Excellence administers the Baldrige Assessment Process for Ohio Organizations.  This year's annual Quest for Success Conference is themed "Celebrate Excellence".  The conference will feature 3 of the 5 national Baldrige Award recipients including Ohio's own PRO-TEC Coating.

Click here for Conference Schedule and Registration

Also, the Ohio Partnership for Excellence is currently accepting applications for examiners for the 2008-2009 award cycle.

For more information on the Ohio Partnership for Excellence and their programs, visit PartnershipOhio.org

 


ASQ Dayton Section 909 Events

There are many happenings just up the road in Dayton that may be of interest to you.  Beyond their monthly Section Meetings, ASQ Dayton is working with the ASQ Customer-Supplier Division to put on a two day Supplier Roadshow Oct 6 and 7.  This will feature two seminars presented by nationally renowned speakers:

  • Supplier Auditing taught by Dennis R. Arter
  • Supplier Certification taught by Richard A. Gould.

Click here for details on the ASQ Customer-Supplier Division Roadshow.

Check out the ASQ Dayton September Newsletter or the ASQ Dayton Website for details on all the happenings in September and October.

 


 

MazuASK MIKE
From Evansville-Owensboro (March08)

The purpose of this column is to help local ASQ members better understand the Society, the local section, the philosophy of total quality management and the tools of quality by allowing section members to send or give questions to Mike. You can contact Mike by calling (812)-853-4893 (W) or (812)-853-9443 (H) or writing to 5311 Woodridge Dr., Newburgh, IN 47630 or Email to pmazu@adelphia.net.

Q. In design of experiments, what are the differences among the various designs?

Design of experiments helps you design an experiment that will provide you with the most information possible with the least amount of work.  The basic principle behind design of experiments is that the experimental trials are well spread out from each other. The way the experimental trials are spread out and the model to be fitted create different types of designs. The most common are: factorial designs, fractional factorial designs, and central composite designs.

Factorial designs are probably the best known designs. They are intended to fit interaction models. The experimental trials are spread out geometrically – they are placed at all of the cube or hypercube corners.

Fractional factorial designs are intended to fit  interaction models with the higher order interactions ignored. They typically fit all of the 2 factor interactions. The experimental trials are placed at the corners, but not all the corners are used, thus producing a more efficient design.

Central composite designs are intended to fit quadratic models. They place their experimental trials at the corners, the center point and on a sphere enclosing the cube above the centers of the faces.

Q. In design of experiments, what is meant by a constraint?

A constraint is a limitation on an experiment. For example, suppose you want to find the best combination of ingredients for a cooling system. The sum of the ingredients must add to 100%. This limitation, or constraint, makes standard designs useless. Standard designs will ask for 100% of each ingredient, for instance. This constraint requires a special design – a mixture design. Mixture designs have the levels for each experimental trial add to 100%.

 


 

FtWayneQUALITY PROCESS UPDATE
G. Daniel Templeton
Fort Wayne, IN



BIG GOAL

This month QPU looks at an eclectic set of issues including some emerging technology. China's quality assurance and control fiascoes have brought the quality profession back into the limelight. How can the profession respond? Four consultants to CEOs provided their short term fixes in the Financial Times. Longer term fixes will include improved teamwork between quality engineers within the supply chain. Emerging examples of successful world-scale teams are being reported in the Wall Street Journal.


A consultant from Bain reminded CEOs that they are accountable personally for the corporate values radiating from their firm. In the long term the best relationships, he said, will be built on a mutually beneficial expectations, not inspections. Further he notes that all employees should feel empowered to resolve problems as they arise.


A PR flack declared that Western companies need to be completely candid about the magnitude of the problem, hiding nothing. These firms then need to the uncompromising in their actions taken with Chinese suppliers. Conversely to the Bain consultant, the PR guy advocates flooding China with inspectors to gauge manufacturing performance. This inspection-heavy process will need to be built into the cost when comparing to other sources of the product. So much for communicating modern thinking to CEOs.


A European MBA professor recommends managers should carry out a full audit of the supply chain, identifying vulnerable links. He scolds that even though outsourced, the supply
chain remains the outsourcing the firm's responsibility. As Nissan found in the UK, permanent supplier development teams yield better results than dealing at an arm's length through an agent or a trading company. However, working with suppliers on quality assurance programs can be costly in terms of management time. The benefit is reduced risk of disrupted supplies. He states that when a process is left to chance, firms may pay an even higher price.

The president and chairman of a software firm advocates improving quality using lean technologies. Giving managers, workers, and suppliers greater visibility and control over the supply chain reduces the risks ranging from political to financial to natural disasters. She forecasts that the next generation of lean manufacturing will be built on open standards,
collaboration, and automation. In her experience, added value in efficient production is becoming a core objective for China’s small and medium-sized producers.

How does one manage a geographically dispersed and disparate team? Often members in one location do not know or trust those and other places. For example, engineers in the US may feel their jobs are threatened by colleagues in Asia. They may hoard information. To overcome such organizational and cultural issues, IBM, Intel, and Tai Ping (a US carpet maker), have found smoother teamwork occurs the projects are split into many small pieces. Each chunk is broken into tasks of about two weeks duration. These tasks are then subdivided into one or two day snippets. This appears to be effective because mistakes and miscommunications are caught quickly. There is also little time wasted waiting for others to finish work. From a technology standpoint, communications tools like interactive bulletin boards, or wikis, allow real time postings with informal communications. Some teams have even adopted andon lights to signify serious problems within a snippet. In terms of organizational development, experts continue to suggest that the team have a common understanding of the tasks and clarify their roles and responsibilities before starting. It is also important to set firm ground rules.

Breaking decisions into stages is a recurring theme in successful business operations. Good managers have always been able to think on their feet. Two examples from different arenas include (a) executing projects during turmoil or when adversity hits and (b) defining treatment options in highly variable illnesses.

Instead of making rock-hard plans and irreversible long-term commitments, researchers are finding that breaking decisions down into stages provides increased flexibility to adjust to changes. The concept of Real Options allows a manager to lay out a series of decisions over a course of a project. Once the project is underway, the managers can account for changes by evaluating each option as the events unfold.

What does this look like practice? Using an example discussed later in an upcoming edition of QPU, the quality assurance manager needs to plan for the introduction of IP6 in about 2010. Briefly, this is an expansion of the current IP address system for the Internet. The quality assurance manager is getting information from the local supplier saying, "This will never happen." Intuitively, and reinforced by websites like DNSstuff.com, it appears as though this could be bigger than Y2K. The manager begins by identifying some options, such as following the Y2K QA playbook, pointing out some critical events that shape the roadmap, or allowing suppliers to take the lead. Each of these options need to have a small monitoring staff, and break down the tasks in a time-ordered fashion. Flexibility costs money. As the picture becomes clearer, at least one of the option paths will become more dominant and the
tasks and sub-options will be parsed more finely. The same process looks and functions very similarly to the Toyota lean product development process. One of the major process improvements in the treatment of cancers in the last 20 years is the introduction of stages into the diagnostic scheme. Physicians credit this standardization step in reducing the variability inherent in assessing and treating cancers. It has allowed modifications of treatments as particular cancers move from one stage to another, or even within the stages. Such
parsing is leading further to expert systems.Some expert systems routinely exceed the accuracy of decisions by human managers. But, that will be a topic for QPU November 07.

The Chinese issues may have brought quality to the top of mind of CEOs, however, government bureaucrats don't even know quality exists. In a recent study of Hot Jobs for Indiana through 2014, quality engineering didn't make the list. It didn't make any list. The Standard Occupational Codes don't even list quality engineering as a separate profession. According
to the government, quality engineers are nearly the same as industrial engineers. Presumably the standard occupational codes were set in place before quality engineers became a distinct profession. Perhaps, a little of the reflected limelight will illuminate some of the dark recesses of government statistics. Fashioning the mirrors sounds like a job for ASQ.

TACTICS

New NDT test concept for fatigue cracks.
From the Detroit area, there is a new hybrid ultrasonic/ infrared nondestructive technique for detecting cracks, called thermosonics. This method uses a brief pulse of low frequency ultrasound (~500Hz) to cause rubbing of the crack surfaces. Rubbing induces frictional heating. The heating is observed through an infrared light video camera. The image of a surface-breaking crack appears in milliseconds after the initiation of the ultrasonic pulse. Subsurface cracks become visible sometime after the pulse. The time is determined by diffusion of the heat from the crack to the surface. Investigators have observed fatigue cracks as short as 20 microns in metal samples.

Energy dispersive X-ray diffraction for semi-quantitative identification of crystals.
This is a variation on classic x-ray diffraction of crystalline materials. The sample rotates instead of the detector. The entire diffraction pattern is measured simultaneously and converted to the chart form using a Fourier transform. About 10% of the patents issued in the last 10 years have involved crystalline materials. Examples of quality assurance applications include detecting counterfeit pharmaceuticals masquerading as "expired" product, detecting the ratio of martensite to austenite in heat-treated steel, recycled plastic identification, lead-based solder or paint recognition, and products that are susceptible to verification under California's Proposition 65. EDXRD is suitable for the determination of lattice orientation of single crystals that is required for growing and processing single crystal materials, like semiconductor single crystals Si, SiC, GaAs and Ge, plus optical lenses as well as industrial diamonds.


LEAN, ISO, AND THE THEORY OF CONSTRAINTS
BY ROBERT JAPIKSE
ASQ Dayton, OH

This article has been presented in three parts starting with the May newsletter edition. Bob is an external 3rd party ISO 9001:2000 and BQ-9000 lead auditor and also does consulting with companies in their total quality system development. He is a member of the Dayton Section If you have any comments or questions, please contact Bob at Rjapikse1@aol.com.

PART III - Back to Lean
We have now eliminated excess WIP, but how does this make use lean? We now know what our true capacity is, and the real rate at which we can do whatever it is we do, by knowing the rate of our constraints. Next we need to determine our customers’ rate of need. This can be tough. A good starting point is the customer’s annual purchases divided by 52 weeks in a year. Can we produce at this rate? If the answer is yes, then terrific. If no, we need to figure out what to do. It is also imperative to know if this rate is seasonal or constant. We need to open up our constraint so we can match demand. Does it need to be opened up year round? Or at certain time periods? It does not matter if it is opened up through capital expenditure, outsourcing/ sub-contracting, or even going back to a previously abondoned labor-intensive way of doing things to increase the output concurrent with the new modern approach. It may cost more per item at this particular stage in the process, but it can be far cheaper in the overall cost of goods sold/performed. The benefits of going lean and working to control your constraints include reduced holding costs, reduced floor space required, faster product turn around, reduced lead time, and reduced scrap. When this approach is applied to office and design processes, things like sales order lead-time, new product to market time, invoice cycle time, and time spent on any other process that is performed, can be drastically reduced.

Where quality comes in
You cannot run a lean system without tight quality control. There is no longer that buffer zone that allows for mistakes. You need to be proactive. If you wait for the problem to work itself out, then it is too late and you will miss your shipment of goods or miss the service you promised to provide. Ok, so how do we make sure we are practive? It comes back to a good strong quality system to do all this effectively. A mix and match patchwork of temporary fixes with everyone doing things just a bit differently will not be albe to meet the demands of running lean. We will now discuss some parts of the system, but keep in mind that the parts themselves are still just parts, and that they need to put togehter into a system. Everything has to be clearly identified, and there needs to be clear, concise, and accurate work instructions for everything done to enable the rapid change from one product/process to another. All information and instructions need to be at the right revision, at the right place, and at the right time. These instructions need to identify what the criteria for acceptance are, and how to let the next step know that the current step has been completed fully and successfully. And if it was not completed successfully? Any scrap that is produced needs to be spotted immediately with mechanisms in place to ensure it goes no further. Keep in mind that scrap can be a bad service component as well as a bad product component. Next, it needs to be carfully analyzed to put controls in place to correct what ever caused the scrap to be created. Once this “scrap corrective action” is in place, it certainly needs to be monitored to verify that it did what you wanted it to do and the scrap has not been regenerated from the same process. This of course would also apply to any defective product or service that is not included in scrap. Any problem would also apply to any defective product or service that is not included in scrap. Any problem (scrap, process error, return, complaint, or other) that requires action needs the follow through to prevent recurrence. There also needs to be a good record and analysis of the instances that may beminor by themselves and not worth addressing, but added together indicate a trend that can an dneeds to be addressed and corrected.

Working outside your organization
To get a fully functioning lean system you will have to work very hard at the relationships with your customers and your vendors. It still does absolutely no good to provide a good or service at improved turnaround time with cost savings to you if it does not meet the customer’s needs. Understanding the customer’s perception of how (or if) you have fulfilled their needs is what will feed right back into the lean process. Consequently, if you do not have confidence in your suppliers, then it is hard to keep everything moving. This is why you need to do some sort of supplier qualification and re-evaluation. You also can very easily find that your suppliers do not want to supply to you in “lean fashion”; that is they are still operating on the “economies of scale” principle. This can be a bit sticky, and many suppliers will not be ahppy when you say you want to reduce your inventory of their product. You will have to convince them taht you will still be buying the same over a period of time; you just want it in smaller batches. Often they will tell you they cannot produce in smaller batches. This should be music to your ears. This is where you started out in the process - “we can only make money if we make big batches”. Many companies have found that this is a good time to go visit the supplier and help them look at ways to become lean as well. Not only will you be working toward getting your raw material in the smaller batches you want to save your holding costs, but you are also helping your supplier to reduce costs and building a strong supplier relationship at the same time. Perhaps reucing your purchase costs?

What does this have to do with ISO?
Let me see, quality system, controls, follow through; sounds like ISO 9001:2000. Is there a part of the Standard we have not discussed? ISO 9001:2000 adds a few things that follow along the same thought processes. One of the biggest is management by information. Measurables need to be put in place after you determine your process. Once you have determined your process flow or plan from the very beginning to the very end (not just on the “production” processes, but everything from initial customer contact to final customer accesptance of finished good or service), then you can set up a measurement plan using the process plan as your road map. Use this map to setup measurables for each process that will in turn support the overall measurables for the whole system. What better way to determine where your constraints are? Once you have determined which particular processes contain constraints you can then set objectives based on the baseline data you collected from your various mesurables. By continuing to measure all your processes you will then see if you have made your objectives and improved the system. If so, great job - now you can start tweaking! You also will probably find that you now see another constraint that was originally hidden by the first one. If you have not made your objecties and have not eliminated the constraint, then you need to do some corrective action to see what can be done.

Final thoughts in the “ISO” section are continued in the Word document of the complete article at the Dayton website at www.asqdayton.org


 

 

image
image