5S Implementation Chart Departmental 5S, Zone wise 5S is best technique to implementation, individual implementation 5S gives advantage to focus on the area that can possible to skip during the implementation, 5S implementation chart is a time chart for the…
5S Audit Schedule 5S Audit Schedule is important part of the 5S Activity & for its implementations. Audit of the 5S Activities done as individual departments, progress of the each stage of the 5S are recording in Audit that…
QMS Awareness Program QMS Awareness Questions Q-01 The process approach to a quality management system seeks to help organization: Manager numerous linked activities. Understand and fulfill requirements. c. Continually improve processes. All of the above. None…
MANAGEMENT PRINCIPLES The management principles individually may be described as: 1) CUSTOMER FOCUSED 1) Understand current and future (Explicit & implicit) customer needs. 2) Plan means to meet these needs. 3) Measure customer satisfaction. 4) Demonstrate continually improved satisfaction. 2)…
BENEFITS OF QUALITY MANAGEMENT SYSTEM-ISO 9001:2015 Benefits (External) Customer Confidence/satisfaction Export Business Competitive Advantage Enhance company’s image in the market. Meet challenges of increasing market globalization. Enhance standardization & interchangeability of components Less – Rejects, Rework, Scrap Less – Administrative…
Training Need Identification Format Training is heart of the industry, reason that all the machinery, equipment, instruments are updating, modifications, amendments, latest technologies are makes a changes in procedure of the operating of machines. Whenever the changes made in…
Doc Audit Plan Final Packaged product Audit Plan – FPPA Plan As we discussed on previous article for the final packaged product audit checklist that cover the requirement of audit and its parameters that need to check during audit…
Doc audit Checklist Final Packaged Product Audit – FPPA Checklist (Doc Audit) International Standards are focus on quality system of product but in case of the packing of product lake the instruction can possible the damage, defect or any other…
Supplier Development plan To comply the requirements of the ISO / TS 16949 & other international standards that focus on the Quality management system not only for the applicant internal system but it also expecting that applicant or achiever’s…
What is process validation? Actually, process validation is key analytical process for ensuring process reliability and capability of consistent to product quality. These procedure defines the values of criteria based on evaluation of data collected from stage of production. Which…