Company Profile:
Cpl are partnered with an esteemed multinational company who are hiring for a Automation Engineer III for their Mayo based manufacturing site for a initial 12-month contract. This is a hybrid position working on a project focusing on the deployment and authorship of recipes relating the system POMSnet. If you're looking to further your career as an Automation/MES Engineer within pharma and enjoys creative problem-solving this could be for. Reach out today for more info.
Job Summary:
The person will maintain the MES (POMSnet) environment; to author and maintain recipes and worksheets for the site. While also providing 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.
Responsibilities:
• Design, create, write and/or make all required changes to MES Recipes, worksheets, equipment and material spec's 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 the Global MES team 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 changes
• Documentation 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.
Essential Requirements:
• Third Level qualification in suitable manufacturing, engineering or business course and/or suitable experience.
• A minimum of 7 years 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.
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