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Internal audit checklists are the checkpoints of different departments to perform an internal quality system audit. It covers all the requirements as per ISO 9001 and IATF 16949 standards with updated sanctioned interpretations. (IATF SIs). All departments like Production, quality, maintenance, purchase, store, marketing, top management, Human resources etc. Internal Audit Checklist for Top Management: … 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
Purpose of internal audit: To establish a Procedure for the Internal Audit of the Quality Management System and to ensure that the Quality Management System confirms all types of internal audits. Type of Audit in the automotive industry: Quality System Audit: The organization’s Processes and their related results comply with planned arrangements and ensure effective … Read more
The purpose of the 8D problem solving methodology is to identify, correct, and eliminate recurring problems, making it useful in product and process improvement. Eight disciplines problem solving (8Ds) is a method developed at Ford Motor Company. Quality engineers use this methodology in the automotive industry. 8 Steps of the 8D problem-solving process D0: Planning … Read more
To close IATF non-conformities received from the IATF auditor, upload the JSON file in the NC Cara portal. The full form of CARA in IATF is Common Audit Report Application. This is the application on the IATF Global oversight website. There are a total of 7 steps for closing the IATF non-conformity on the NC … 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
