Simplifying Quality – Driving Excellence.
mksharma 
Purpose: Coherence between all the documents, such as the Customer Inspection Standard of parts with the Control Plan, Operation Standard, Inspection Standard, and packing Standard, is essential. Properly defining the standards can prevent rejection and rework and thus improve OEE and COPQ. Responsibility : S.No Activity Responsibility Frequency 1 Review of the Standards/ Format/ … Read more
Purpose: To understand clearly abnormality and abnormal situations, to make operators understand abnormality and abnormal situations, and to standardize further the rules and routes to handle such situations. To learn about handling abnormality in quality. Scope: Handling in-process complaints, supplier complaints & customer complaints and abnormal situations. Abnormal situation: An abnormal situation occurs when a … Read more
Process Capability Process capability is a statistical measure of the ability of a process to consistently produce output within specification limits. It quantifies the ability of a process to meet customer requirements and expectations. It is done by assessing the spread and centering of process output relative to predetermined specifications. Process capability is a statistical … Read more
5S is a five-step program that is done in sequential order. 5S is a series of activities for eliminating waste that contributes to workplace rejections, mistakes and injuries. The Japanese factories are so clean that you can eat off the floor. This is simply a matter of pride for the Japanese. Below are the 5 … Read more
The International Automotive Task Force (IATF) 16949 is a quality management system standard specifically developed for the automotive industry. Following is the list of major changes in the IATF 16949:2016 standard (New Requirements regarding ISO/TS 16949:2009):- You may like to read more about: Corporate responsibility policies. The latest version of the standard, IATF 16949:2016, has … Read more
Standard operating procedures (SOP) and a Control Plan are critical for a manufacturing process. SOPs are detailed work instructions to help workers carry out routine jobs. A Control Plan is a documented description of the systems and processes required for controlling the manufacturing of a product. But there are some differences between SOP and Control … Read more
Attribute MSA Study: Attribute MSA is a tool used to evaluate the measurement system when attribute (qualitative) measurement is to be done. In the attribute MSA study, we check that the measurement error is within an acceptable level before doing the SPC study. Attribute and Variable in MSA: Attribute Data (Qualitative): Variable Data (Quantitative): Types … Read more
Purpose: To establish & maintain a documented procedure that ensures production works under controlled conditions, to meet customer requirements. Scope: Applies to all types of products manufactured in the company ( Press shop, weld shop, machine shop, paint shop, assembly shop etc) Responsibility: The Production Head & supervisors are responsible for the implementation of this … Read more
Purpose of FMEA: The purpose of FMEA is to establish & maintain a procedure for process failure. Scope of FMEA: This procedure applies to all processes (major & critical) that are being used to make various products. What is an FMEA process? An FMEA process can be described as a synchronized group of activities … Read more
