Management role in QMS,EHS
Management commitments, Role & Responsibility: Quality management System (QMS) + Environment Health & Safety (EHS) What should management commitments, role & responsibility in Quality management system & Environment health & safety purpose, its important part to implements any system…
Process Flow Chart
Process Flow Chart How to create process flow chart? Process flow chart is prototype of the processes are established, implemented & maintained in organisation, PFD ( Process flow chart) or Process flow diagram is mirror of the production…
Vendor Audit: Why vendor audit is necessary?
Vendor Audit: Why vendor audit is necessary? What is vendor audit? A vendor audit is audit of supplier’s internal system to ensure that purchasing materials are complied with all quality, technical, statutory and regulatory requirements. Group of…
Preventive maintenance schedule
Preventive maintenance schedule: maintenance Task What is Preventive maintenance schedule? Preventive maintenance schedule is advance planning for maintenance to eliminate possibility of failure of machine or equipment. It can schedule daily, weekly or half monthly for each machine as…
Failure Mode Effects Analysis
FMEA overview Failure definition: A ‘Failure’ is that a component, assembly or system which does not meet the requirements or function in accordance with design intent. (Ex. Not meeting the specification, heat treatment failure) Failure Mode definition: A ‘Failure Mode’…
APQP
APQP stand for Advance Product Quality Planning Quality… Product………Planning…… “Planning to deliver Quality product for new product development” What is APQP? Advance Product Quality Planning is a structured & systematic method of defining and establishing the steps necessary to assure…
ISO 9001: 2015 under revision: Standards for Organization
ISO 9001: 2015 under revision: Standards for Organization ISO 9001 very popular standard are used by billions of people and millions of organization over the world, after success of the ISO 9001:2008 is revised with a huge impacts can be…
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 for each one. 5S Corrective action report Overview to…
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, major repairs, layout changes & major tooling changes. What is…
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, to find inadequate circumstances from manufacturing processes. Overview Manufacturing process…