derphinjerry
-Maintain the Quality Management System (QMS) factory and its effectiveness by doing all the document control activities and follow up the documents for the management review sessions. -Preparing Inspection and Test Plan / Check Sheets and ensuring approval from Client. -Ensuring that all Contractual / Company and local authority requirements for Quality, Health, Safety and -Environment (HSE) requirements are complied with ensuring the implementation of the Company and Project Quality System / Plan. -Ensuring all Inspections are done as per Inspection and Test Plan / Contract and that these are documented on pre-defined formats / Check Sheets. Ensuring all hold and Witness Points have adhered to the Client is given sufficient notice for Inspection. -Ensuring incoming materials are inspected, as approved and stored properly as recommended. - Ensuring proper interaction and co-ordination with Client, Site Laboratory and Site Team for Project co-ordination. -Ensuring all Quality requirements are understood by site personnel/workman and sub-contractors and providing training in the quality systems and skill functions necessary. -Ensuring and co-ordination for the sub-contractors quality control/implementation on site. -Ensuring proper control on receipt/ distribution of Contractual Documents and Drawings with assistance from Document Controller. -Ensuring all valid documentation/contract documents are being used on the site. -Carrying out regular surveillance inspection for activities on site and that of sub-contractors. -Monitoring non-conformances and following up with site team for close out. Ensuring corrective/preventive actions are taken to avoid repetitions of non-conformances. -Prepare where necessary, statistical data which will show quality trends. -Implementation of the objective set during management review. -Reporting weekly quality performances and documentation to Quality Manager. -Responsible for reviewing all quality records on site and retaining them in handover files. -Ensuring preparation of Final Handover Documentation and submissions of quality related documents.
