Cooperating with the System Development Group to create the documents related to the Quality Management System, to ensure the continuity and required corrections and granting the quality approval. Keeping the current revisions of all documents required for, internal audit, ISO 9001 (2015), BRC, 14001, HACCP,Sedex, Quality Management System at the place of use as the controlled copies; maintaining the original versions. Preparing, implementing and following up the Internal Audit Plans for all the affiliated units. Creating quality instructions for the assessment of input, process and products. Requesting the creation of all the corrective/preventive actions from the responsible units, follow-up
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