1.Responsible to support Site Quality System activities by coordinate with site departments to comply with ISO9001 requirements , TE Quality Policy, Manual and Standard Procedures.
2.Maintain and develop quality system documents, records, provide evaluation results and non-compliance issues to management team for continuous improvement and system sustainability.
3.Have been assigned as Site Record Coordinator to serves as a liaison between the Corporate Records Coordinator and Department.
4.Records Coordinator at site on Local Process Development, IMS and Document Management Program included conduct/provide training program and guidance to local
Department Records Coordinator on document management processes.
5.Conduct site internal audit program, management review and training program to all employees including new comers and subcontractors on ISO principles and requirements.
6. Arrange for establishing classification/registration as required by national legislation based on as well as the procurement any additional data as needed.
7.Support PEHS activities as site representative to make sure that all new/existing products are in compliance with Hazardous Substance Act 2535, local laws and regulations.
8.Liaise with external parties such as DIW , TISI, THTI, FDA, etc. To comply permission processes related with local laws and regulations before it is manufactured,imported or exported.
9.Responsible to update local permission/licenses list, local rules and regulations, report to Site Management team and update to Regional ITC.
10. To support custom and export administrations processes (clearing) licensing, tariff declarations and documentations) case by case.
11. Other assignments or special projects as required by Quality System Manager and Site Manager.