MES Engineer (Senior) – Westport Responsibilities Maintain the MES (POMSnet) environment; author and maintain recipes and worksheets for the Westport 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.Design, create, write and/or make all required changes to MES Recipes, worksheets, equipment and material specifications including phase transition logic.Design, create, write and execute test and validation protocols, risk assessments, and system documentation.Ensure cleaning, equipment and product procedures are aligned to MES processes.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.Support other MES system users 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 changes.Document all activities in line with cGMP requirements.Cross train within the team and train new team members.Participate in continuous improvement programs to implement improvements in quality, safety, environmental, and production systems.Adhere to and support all EHS standards, procedures, and policies.Top Skills Required MES recipe authoring experience using POMsnet or another MES system.SAP experience and proficiency in MM, PP, and IM modules.Pharma experience, understanding of GxP.Ability to resolve technical problems and manage project implementations.Requirements Third Level qualification in suitable manufacturing, engineering or business course and/or suitable experience.A minimum of 7 years authoring experience with technical lead on multiple implementation projects.Proficient with MES application and configuration rules including interfacing (preferably POMSnet).Experience in batch processing operations in an FDA/HPRA regulated industry with strong knowledge of cGMP and regulatory requirements.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 ensure compliance with procedures.For more information and a confidential chat, feel free to reach out to me at ****** or call me on 01-482 5494.
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