5 WHY – an iterative interrogative technique used to explore the cause-and-effect relationships underlying a particular problem.
Example: Castings are piling up behind a trim press.
Why? Because some parts need to be run through the press a second time to remove all the flashing. Why? Because the machine’s blades aren’t that sharp. Why? They haven’t been replaced or reconditioned. Why not? It isn’t part of the regular preventive maintenance plan.
Solution: replace the blades and set a schedule for regularly maintaining that machine.
The five S methodology helps a workplace remove items that are no longer needed (sort), organize the items to optimize efficiency and flow (straighten), clean the area in order to more easily identify problems (shine), implement color coding and labels to stay consistent with other areas (standardize) and develop behaviors that keep the workplace organized over the long term (sustain).
Action Tracker – A spreadsheet that helps in managing a project. An action tracker lists the open issues, actions retired, owner responsible for completing that action item and the due date of completion.
Caster – A small wheel attached to the bottom of something, such as heavy piece of furniture, to make it easier to move. (source)
CE Mark – CE marking is a mandatory conformity marking for certain products sold within the European Economic Area (EEA) since 1985. The CE marking is also found on products sold outside the EEA that are manufactured in, or designed to be sold in, the EEA. This makes the CE marking recognizable worldwide even to people who are not familiar with the European Economic Area. It is in that sense similar to the FCC Declaration of Conformity used on certain electronic devices sold in the United States.
The CE marking is the manufacturer’s declaration that the product meets the requirements of the applicable EC directives.
Concept Generation – The most critical step in the design engineering process. It is a procedure that begins with a set of customer needs and target specifications and results in an array of product concept design alternatives from which a final design will be selected. (source)
Continuous Improvement (CI) – A process of manufacturing which is a subsection of just-in-time manufacturing and lean manufacturing encompassing group technology. The goal of cellular manufacturing is to move as quickly as possible, make a wide variety of similar products, while making as little waste as possible.
CSA Mark – CSA International certification marks indicate that a product, process or service has been tested to a Canadian or U.S. standard and it meets the requirements of an applicable CSA standard or another recognized document used as a basis for certification.
Design for Manufacture and Assembly (DFMA) – the process of proactively design products to optimize all the manufacturing functions: fabrication, assembly, test, procurement, shipping, delivery, service, and repair, and assure the best cost, quality, reliability, regulatory compliance, safety, time-to-market, and customer satisfaction. (source)
Empathetic design – The process of developing an understanding of users, not just their overt needs, but of their constraints, practices, problem-solving approaches, contexts, and the interrelations between people as a whole. (source)
Ergonomics (or human factors) – The scientific study of people at work. The goal of ergonomics is to reduce stress and eliminate injuries and disorders associated with the overuse of muscles, bad posture, and repeated tasks. This is accomplished by designing tasks, work spaces, controls, displays, tools, lighting, and equipment to fit the employee’s physical capabilities and limitations. (source)
Fixed Repeating Schedule – a production schedule which is unchanging and repeated daily or over a longer period, such as two weeks or a month. If the schedule can be implemented, then economies of repetition start to become evident and suppliers and customers can be assured in their own activity scheduling.
Genchi Genbutsu – a Japanese term meaning “go and see for yourself.” The notion is that rather than simply hear or read about a problem and make a suggestion for improvement, one should go to its direct location and experience the situation firsthand.
High-level Assembly – A proven operations strategy that allows OEMs to focus its in-house efforts on the top-level assembly to simplify production, minimize inventory, floor space, manufacturing overhead and direct labor. (source)
Human Machine Interface (HMI) – A component of certain devices that are capable of handling human-machine interactions. The interface consist of hardware and software that allow user inputs to be translated as signals for machines that, in turn, provide the required result to the user. (source)
IEC 60601-1 – A series of technical standards for the safety and effectiveness of medical electrical equipment, published by the International Electrotechnical Commission (IEC). (source)
ISO 13485 – Specified requirements for a quality management where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements set by the International Organization for Standardization (ISO). (source)
ISO 9001 – A set of international standards on quality management and quality assurance developed to help companies effectively document the quality system elements to be implemented to maintain an efficient quality system. (source)
ISTA Packaging Testing – International Safe Transit Association (ISTA) packaging tests are used to assess the security of goods during transport by using vibration, impact, drop and temperature testing. This testing mimics transportation conditions to gauge the likelihood of goods being damaged during transit. (source)
Kaizen – Originated from Japanese philosophy that simply translates to “good change”. It is the idea of not focusing on everything all at once, but focusing on small, incremental improvements to make sustainable change.
Kanban – A Japanese manufacturing system in which the supply of components is regulated through the use of an instruction card sent along the production line. (source)
Production Part Approval Process (PPAP) – A standardized process in that helps manufacturers and suppliers communicate and approve production designs and processes before, during, and after manufacturing.
Quality at the Source – a lean manufacturing principle which defines that quality output is not only measured at the end of the production line but at every step of the productive process and being the responsibility of each individual who contributes to the production or on time delivery of a product or service.
Quality Managment System (QMS) – is a set of policies, processes and procedures required for planning and execution (production/development/service) in the core business area of an organization (areas that can impact the organization’s ability to meet customer requirements) ISO 9001 is an example of a Quality Management System.
Quick Response Manufacturing (QRM) – A company wide strategy to reduce lead times in all phases of manufacturing and office operations. It can bring your products to the market more quickly and help you compete in a rapidly changing manufacturing arena. It will increase profitability by reducing cost, enhance delivery performance and improve quality.
Return on investment (ROI) – with respect to a project, or Project ROI, is an indicator used to measure the financial savings/gain (or loss) of a project in relation to its cost. Typically, it is used in determining whether a project will yield positive financial benefits and in turn be given approval to proceed. Project ROI = (Financial Gain or Loss – Project Cost / Project Cost) X 100.
Single Minute Exchange of Die (SMED) – provides a rapid and efficient way of converting a manufacturing process from the current product to the next product. This rapid tool changeover is key to reducing production lot sizes and thereby improving flow.
Unique Device Identification (UDI) – A standardized numbering and traceability system for medical devices to facilitate rapid and accurate identification of a medical device and clearly document the device.
UL Listing – UL Listing means that UL (Underwriters Laboratories) has tested representative samples of the product and determined that it meets UL’s requirements. These requirements are based primarily on UL’s published and nationally recognized Standards for Safety. References to UL and the UL Listing may include: the UL Listing Mark.
Validation & Verification (V&V) – A set of processes ensuring that the design intent meets client and regulatory requirements. The FDA will routinely request that OEMs provide all product documentation (including records, designs, drawings, approved Production Part Approval Process (PPAP) results, etc.) within 24 hours.
Waste – Anything the customer is unwilling to pay for including defects, overproduction, waiting, non-utilized talent, transportation, inventory, motion, and extra-processing. The main wastes are seven (7W):
W1 – Overproduction
W2 – Inventory
W3 – Waiting
W4 – Transportation
W5 – Motion
W6 – Process (useless steps in a process)
W7 – Defects
Work In Progress (WIP) – sometimes referred to as work in process, is the sum of all costs put into the production process to manufacture products that are partially completed. WIP refers to raw materials, labor and overhead costs incurred for products that are at various stages of the production process.