5S Corrective Action Report

A 5S corrective action report is document use to proceeding actions to eliminate defects from the product or process. This report may includes a non-conformance details, root causes and solutions…

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Process change review checklist

Process change review checklist   What is Process change review checklist? Process change review checklist is document for verification of implemented changes in organization. A document covered new processes, machine,…

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Manufacturing Process Audit Checklist

Manufacturing Process Audit Checklist: Check sheet/ Template / Checklist Format What is manufacturing process audit? Manufacturing Process Audit Checklist is specifically defined checklist format for audit manufacturing processes and sequences,…

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Calibration Calendar for Instruments

Calibration Calendar for Instruments As basic requirements of QMS Systems (ISO 9001, TS 16949 etc..) having a clauses & needs of clauses in manual system that any organization which had…

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Vendor Registration form – Simple format

Vendor Registration Form :  Simple Sample | Example | Format    Probably, individually each company has its own registration form & details as requirements of serious concern to product realization,…

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Machine History Card

Machine History Card – Maintenance task Maintenance department  important part of the company, maintenance need a much awareness, perfection,  any king of retake can be costly if mistakes occur in…

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Risk Analysis: How to classify and Estimate risk

Risk Analysis: How to classify and Estimate risk   Risk’s perfect definition is very hard to explain, for one organization particular risk be little impact & for second organization loss…

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