Quality Monitoring
Collecting data through regular measuring and visual inspections ensures that all of our products and processes meet our customer's requirements.
Frequent inspections are used in all stages of the fabrication process to prevent improper use of equipment and to prevent the delivery of products that do not meet the desired specifications.
Documentation
Records are maintained to provide evidence of inspections conducted on received and processed products. Our records identify the individual(s) who conducted the inspections and whether or not the product passed or failed the inspection.
Our documentation that is kept on file includes inspection forms, Job Task Procedure Manuals (JTP's), as well as data from internal and external resources. Documents of this nature are reviewed annually to determine if any revisions need to be made.
Continually Improving Our System
Greenpak recognizes the need for prompt and effective, corrective and preventive action to maintain and improve upon our quality assurance system. When monitoring and inspections indicate that specified requirements are not being met, immediate corrective action is taken. Procedures and processes are addressed and corrected or improved upon. Individual products that do not pass inspection are segregated from acceptable products and tagged until an appropriate method of correction is determined by management.
Internal Quality Audits
To determine the level of compliance to the specified customer requirements, Internal quality audits are performed in accordance with our (Internal Quality Audit Job Task Procedures). These audits serve as an important monitoring tool in evaluating the effectiveness of our quality assurance system.
Audit Results
Audit results are documented and reported to management. Corrective actions are specified to correct any deficiencies uncovered during the audit. Follow-up audits will record the effectiveness of the corrective action. |