Senior MES Engineer and MES Engineer contract rolesScroll down to find the complete details of the job offer, including experience required and associated duties and tasks.Our Pharmaceutical client in Wesport, Country Mayo are recruiting for a senior and a mid-level MES Engineer for 12 month contracts.PurposeMaintain the MES (POMSnet) environment; to author & maintain recipes & worksheets for Westport site.Troubleshoot and provide solutions for MES & SAP problems in recipe execution and recipe authoring.
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 documentation.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-arounds and fixes identified.Liaise with Abbvie Global MES on Westport required system improvements.Provide support to other MES system users as required to ensure business continuity.Participate in NPI projects from initiation to ensure MES system or hardware requirements are taken into consideration.Keep other recipe authors up to date on MES changesDocumentation of all activities in line with c GMP requirements.Cross training within the team and training of new team members.Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.Adheres to and supports all EHS standards, procedures and policies.
RequirementsThird Level qualification in suitable manufacturing, engineering or business course and/or suitable experience.Mid-level role - minimum of 2 years authoring experience preferably using POMSnet.Senior role - minimum of 7 years authoring experience and has led or was technical lead on multiple implementation projects.Be 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 c GMP and regulatory requirements relating to the pharmaceutical industry.A good knowledge of IT systems is required for this role.
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xyswxtq If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement.To find out more about Progressive please visit Progressive Recruitment, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2 N 4 BQ, United Kingdom | Partnership Number | OC(phone number removed) England and Wales