Premium Freight Monitoring report
Premium Freight Monitoring report Its can be key objective or key performance indicator for sales depart or company level objective that need to monitoring on high level, reason it premium freight is a expenses that not real or legit…
List of Critical Spare Parts Format
List of Critical Spare Parts Format Machines are working frequently & possible that works round o’clock, at any movement any part of the machine can be broke and machine shutdown due to it, if the parts are available…
PDCA
PDCA ( Plan – Do – Check – Act ) PDCA stand for Plan-Do-Check-Act or also refer as Plan-Do-Study- Act is cycle. PDCA method is used in business concept are also merged with various methods, systems that help to…
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…
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…
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 applied for QMS, EQMS that need to calibration its instruments…