7 steps of practice for implementation of management responsibility process in ISO 9001
Implementation of management responsibility process in ISO 9001, this method provides basic guidance for effectively implementation of process to define management responsibility in ISO 9001 quality system requirements. (1) Role of Management in Quality objective The management team must ensure…
Management responsibility for quality management system
To effectively implementation of ISO 9001 / Quality management system in organization, management commitment is much important. More, management should involves in each major activity to effective and continual improvement. Overview This article describes the management commitment for the quality…
Quality operating system – Procedure & Methodology
Quality operating system – Procedure & Methodology A quality operating system is a methodology. QOS disciplined approach works systematically to standardized business practices and operate new product development and manufacturing operations. Overview Most organization are expecting health management system for…
how to maximize utilization of resources, facilities and tools
Utilization of resources | The procedure is needs to establish for implementation of manufacturing processes & product quality through identification & improve facilities, resources utilization. Introduction The process used for identify new machine, facility and tools which are in use…
Product NC documentation
Product NC documentation Product NC documentation is prepared for managing records of non conformance identified in manufacturing processes with product concern. Product NC documentation is established by quality department to recording product non conformance during the inspection at various stages…
Guidance Document for problem reporting – problem solving documents
Guidance Document for problem reporting – problem solving documents Problem reporting is documentation process that used for manage information of identified problems, and provides details to concern department for resolve the issue raise. The report is part of problem solving…
Relation between CAPA & non-conformity
CAPA & non-conformity : The processes describe relation between corrective actions & preventive actions (CAPA) with non-conformity (NC) for stability of quality management system. The purpose of establish and maintain a process for corrective actions is to reducing…
Continuous improvement objectives
Continuous improvement objectives: The purpose of developing this procedure is to ensure that organization sets objectives appropriate targets are sufficient to achieve determined achievements. What is quality objective? Quality objective is overall goal that an organization setup it…
Continuous improvement project | Quality System
Continuous improvement project establish by quality team to increase resources productivity, quality products and structural working environment in organization. Continuous improvement project is requires to establish by quality team. To increase resources productivity, quality products and structural working…
What is an inspection levels in Quality system – ISO 9001 & TS 16949
The inspection levels designates the relative amount of inspection. Normally sample guideline provide a technique to identifying the different levels of quality inspection and priority. Overview to Inspection levels In the manufacturing unit, engineering or any other unit that needs…