Job Description
We are are looking to hire a MES Systems Manager to join our MES team working at our client site, a pharmaceutical MNC. The selected candidate will be required to provide consultation and engineering service to the execution phase of the project. He/she will also be involved in the generation and ownership of IQ/OQ/PQ documentation and the GoLive Support. Responsibilities Troubleshoot and provide solutions for MES & ERP problems in recipe execution and recipe authoring. Liaise with QA to provide approved change control documentation for all MES system changes. Design, create, write and execute to a high-quality standard, test and validation protocols, risk assessments, and system documentation. Design, create, write and/or make all required changes to MES & ERP Recipes, worksheets, equipment and material spec's including phase transition logic to a high-quality standard. Design, create, write and/or make all required changes to ensure cleaning, equipment and product procedures are aligned to MES processes and vice versa. Design, create, write and provide training for all other site personnel on their related MES roles and arrange system access. Participate in MES knowledge exchanges, MES Governance meetings and manage issues, work-around and fixes identified. Work closely with IT regarding upgrades, patching, hardware support, security and system access and provide technical expertise in implementing upgrades and patching. Liaise with Global MES on required system improvements. Provide support to other MES system users as required to ensure business continuity. Participate in MES projects from initiation to ensure MES system or hardware requirements are taken into consideration. Ensure maintenance/replacement of MES hardware, printers, scales, scanners and bar-code labelers. Review for upgrades periodically. Keep other MES Team Members up to date on MES changes Documentation of all activities in line with cGMP requirements. Cross training within the team and trainin
