Réalta Technologies are seeking an experienced MES Engineer to support the design, implementation, and optimisation of MES solutions within a regulated pharmaceutical manufacturing environment in Co. Louth. The successful candidate will work closely with manufacturing, quality, and IT teams to translate business and operational requirements into robust MES solutions that replace manual or paper-based processes. Key Responsibilities Provide organisational oversight for complex systems involving the development of MES solutions. Work closely with business management and users to define the needs and design solutions that add value to the company. Gather user requirements in relation to controlling and recording manufacturing activities. Map existing manufacturing process to the MBR design. Design and deployment of MES systems to replace paper based or manual systems in a pharmaceutical environment and integrate with ERP and control equipment. Documentation of MES configuration and validation of EBRs Implementation of MES solutions and integration with ERP and control equipment Required to comply with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions. Work collaboratively to drive a safe and compliant culture on site. Required Skills & Experience 5 years’ experience working with MES systems within pharmaceutical, biotechnology, or other regulated manufacturing environments. Experience gathering and translating user requirements into MES functional designs and system configurations. Strong understanding of manufacturing processes and batch execution, including mapping processes to Master Batch Records (MBRs) and Electronic Batch Records (EBRs). Experience designing and deploying MES solutions to replace paper-based or manual manufacturing systems. Knowledge of MES integration with ERP systems and plant control equipment (e.g. PLCs, SCADA, DCS). Experience supporting system validation and documentation, including configuration documentation and validation of EBRs in accordance with regulatory requirements. Strong knowledge of cGMP, regulatory compliance, and pharmaceutical quality standards. Ability to collaborate with cross-functional teams including manufacturing, quality, automation, and IT stakeholders. Excellent problem-solving, communication, and stakeholder management skills.