Automation/ MES Engineer (Mid-level) – Westport- 27096 23 Month Contract Requires 2 years experience within the Pharma industry, will be involved in MES recipe creation, verification and authoring in POMsnet and daily production support/management and troubleshooting.
Working knowledge of SAP is required as it is linked to POMsnet, which tracks the movement of materials and creates an electronic batch record. Any persons/actions related to this record are captured in EBR. Project management experience is a bonus.
ResponsibilitiesDesign, 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.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 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.RequirementsThird Level qualification in a suitable manufacturing, engineering or business course and/or suitable experience.Familiarity 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 is an advantage.Proven attention to detail and mental concentration to ensure total compliance with procedures at all times.
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