REQUIREMENT . Support the generation of cGMP documentation including qualification protocols, SOP and production batch record issuance. . Co-ordinate internal review and approval of documentation. . Proactively progress documents to achieve schedule adherence and to site policies & compliance with cGMP's. . Initiating Production Change control, deviation, and handling of related CAPA activities, task implementation using Trackwise. Assist in the preparation of reports/presentations as required. . To update and format documentation including SOPs, forms, logbooks, and label templates. . Prepare label templates and print labels as required for finished product. . Write/review manufacturing documentation (SOPs, Manufacturing Records & Logbooks) ensuring it is current, accurate and in accordance with regulatory requirements. . Track and trend relevant technical and business process metrics to ensure operations are performing effectively and efficiently. . To arrange quotation and purchase ...