MES Engineer

Overview

We are seeking a skilled MES Engineer to join a leading global biotechnology company based in Dublin, Ireland. This role offers the chance to advance your career in the life sciences sector by contributing to the development and implementation of Master Batch Records (MBRs) within manufacturing processes.

Key Responsibilities

• Develop, configure, and test Master Batch Records (MBRs) from initial concepts through to final design, focusing on Form/Fill and Packaging areas to support current commercial products and new product launches.
• Lead design review sessions for MBR development, coordinating with Operations, Process Development, and Quality teams to ensure alignment and quality.
• Create, execute, and assess Application Lifecycle Management test scripts and test sets to validate MBR designs effectively.
• Provide ongoing support and enhancements to the MES system for MBR development and streamline MES business processes.
• Deliver training programs for Electronic Batch Record (EBR) end-users, including Supervisors, Operators, and Technical, QA, and Support staff.
• Develop, review, and update Standard Operating Procedures (SOPs) related to MES operations.
• Manage MBR change requests promptly, including preparation and documentation, coordinating with stakeholders such as customers and system owners.
• Ensure compliance with timelines and performance metrics for change control and CAPA processes.
• Design, configure, and test equipment integrations to facilitate MBR interactions with shop floor equipment, including OSI PI, Siemens Recipe Managers, Rockwell, and Kepware OPC Server systems.
• Troubleshoot interface errors and address stock discrepancies between ERP and MES systems as needed.
• Collaborate with the MES core team to innovate and improve operational workflows.
• Provide technical support as required under the direction of Operations leadership.
• Carry out additional duties assigned by the Executive Director of Patient Supply or senior manufacturing managers.

Qualifications and Experience

• Bachelor's degree in Engineering or Science disciplines.
• Extensive technical experience with MES systems in a manufacturing environment.
• Experience or capability to quickly learn and adapt to Syringe and Vial manufacturing operations.
• Demonstrated ability to adjust rapidly to the unique demands of Syringe/Vial filling processes.
• Familiarity with regulatory standards relevant to the industry, including GMP and EH&S.

Benefits

• Competitive salary package
• Access to pension contributions
• Health insurance coverage
• Paid holiday entitlements

Work Location

The position is based in Dublin, Ireland with onsite presence required.