OverviewMES Engineer - Ireland, Westport - 12 Months ContractLocated on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for an MES Engineer to join their state-of-the-art pharmaceutical facility. They have invested $55 billion in research to discover and develop new medicines in the pursuit of scientific breakthroughs and changing people’s lives. They have 50,000 employees around the world and are continuing to grow.ResponsibilitiesDesign, create, write and/or make all required changes to MES recipes, worksheets, equipment and material spec's including phase transition logicDesign, create, write and execute, test and validation protocols, risk assessments, and system documentationDesign, create, write and/or make all required changes to ensure cleaning, equipment and product procedures are aligned to MES processes and vice versaDesign, create, write and provide training for all other site personnel on their related MES roles and arrange system accessParticipate in MES knowledge exchanges, MES Governance meetings and manage issues, work-around and fixes identifiedProvide support to other MES system users as required to ensure business continuityParticipate in NPI projects from initiation to ensure MES system or hardware requirements are taken into considerationKeep other recipe authors up to date on MES changesDocumentation of all activities in line with cGMP requirementsCross training within the team and training of new team membersParticipation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systemsAdheres to and supports all EHS standards, procedures and policiesQualificationsDesirable Experience:Third Level qualification in suitable manufacturing, engineering or business course and/or suitable experienceRequires extensive authoring experience preferably using POMSnetBe familiar with MES application and configuration rules and requirements including interfacing (preferably POMSnet)Experience of batch processing operations in an FDA/HPRA regulated industry. Strong knowledge of cGMP and regulatory requirements relating to the pharmaceutical industryA good knowledge of IT systems is required for this roleSAP knowledge/experience in MM, PP and IM modules an advantageProven attention to detail and mental concentration, to ensure total compliance with procedures at all timesIf this role is of interest, please apply now!#LI-JS4
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