1 day ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.Direct message the job poster from PE GlobalSenior Recruitment Consultant at PE GlobalPE Global is recruiting for a MES Engineer on behalf of our biopharmaceutical client in County Mayo. This is an initial 12-month contract, hybrid role.Job SummaryMaintain the MES environment; to author and maintain recipes and worksheets for the site.Provide technical guidance and solutioning to other MES Engineers.Act as site escalation point for complex or challenging troubleshooting or recipe design.Provide project management guidance and expertise to the MES function.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 Global MES on 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 cGMP 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.A minimum of 5-year’s authoring experience and has led or was technical lead on multiple implementation projects.Be proficient 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 industry.A good knowledge of IT systems is required for this role.SAP knowledge/experience in MM, PP and IM modules.Proven attention to detail and mental concentration, to always ensure total compliance with procedures.Interested candidates should submit an updated CV.Please click the link below to apply, call Paul Wheatley on 083 094 0199 or alternatively send an up-to-date CV to paul.wheatley@peglobal.net***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***Seniority levelSeniority levelAssociateEmployment typeEmployment typeContractJob functionJob functionEngineering, Information Technology, and ScienceIndustriesPharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment ManufacturingReferrals increase your chances of interviewing at PE Global by 2xGet notified about new Manufacturing Specialist jobs in Westport, County Mayo, Ireland.Westport, County Mayo, Ireland 6 days agoWestport, County Mayo, Ireland 5 days agoBiologics (Manufacturing) Technical Shift LeadWestport, County Mayo, Ireland 5 days agoWestport, County Mayo, Ireland 5 days agoCastlebar, County Mayo, Ireland 1 week agoCastlebar, County Mayo, Ireland 5 days agoWestport, County Mayo, Ireland 5 days agoWe’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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