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To close IATF non-conformities received from the IATF auditor, upload the JSON file in the NC Cara portal. CARA in IATF is the Common Audit Report Application. This is the application on the IATF Global oversight website. There are 7 steps for closing the IATF non-conformity on the NC CARA portal. 7 steps to close … Read more
The Seven Quality Control (QC) tools are graphical techniques for identifying and solving problems in manufacturing and other industries. Below are the benefits of each of the 7QC tools separately: Benefits of Flowcharts: Benefits of check sheets: You may like to read about the Check Sheets Benefits of Pareto charts: You may like to read … Read more
List of mandatory procedures for IATF 16949: IATF 16949:2016 is the latest version of IATF 16949. There are 21 documented mandatory processes and 282 ‘Shall Requirements’ in IATF 16949. Below are the IATF mandatory procedures. Process Description Clause No Product Safety 4.4.1.2 Calibration 7.1.5.2.1 Competence Training 7.2.1 Internal Auditor Competency 7.2.3 Employee Motivation 7.3.2 Engineering … Read more
Purpose: To ensure that the personnel performing work affecting product quality are competent based on appropriate education, training, skill & experience. Also to motivate employees to achieve quality objectives, continual improvement and create an environment to promote quality culture and innovation. Scope: This procedure relates to all personnel carrying out activities affecting the quality of … 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
Control Plan The Control Plan in Quality is a documented description of the systems and the processes required for controlling the manufacturing of the product as per the IATF 16949 standard. A control plan is the main document of the PPAP (Production Part Approval Process). The control plan covers all processes per PFD and PFMEA … Read more
ISO 9001:2015 defines the fundamental quality management system requirements for all organizations. It was prepared and managed by the International Organization for Standardization. IATF 16949 is an automotive QMS standard along with applicable customer-specific requirements. It was developed by the IATF (International Automotive Task Force). However, IATF 16949 is not a stand-alone standard but a … 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 attribute MSA study we check the measurement error is within an acceptance level before doing SPC study. Attribute and Variable in MSA: Attribute Data (Qualitative): Variable Data (Quantitative): Types of MSA: 1. … Read more
Quality Management Principles: QMS principles are a set of fundamental beliefs, norms, rules and values that are accepted as fine and can be used as a basis for quality management. The principles can be used as a foundation to guide an organization’s performance improvement. They were developed and updated by experts of ISO/TC 176, which … Read more
Poka-Yoke: Poka Yoke means Mistake Proofing or Error Proofing. Poka Yoke is a mechanism to prevent mistakes and defects from being made or detect mistakes if not prevented. It is also called error-proofing or foolproofing. Dr. Shigeo Shingo developed the concept of Poka-Yoke. Poka-Yoke is based on the concept that people do not make mistakes intentionally. … Read more