Réalta Technologies is seeking a skilled DeltaV Automation Engineer to join our growing team. In this role, you will be instrumental in the design, development, and implementation of control systems for a leading pharmaceutical client based in Limerick. This is a fantastic opportunity to apply your expertise in DeltaV automation within a highly regulated and innovative biopharma environment. Key Responsibilities: Lead the design and implementation of DeltaV control systems within pharmaceutical manufacturing environments.Collaborate closely with System Integrators, Engineers, and Developers to ensure efficient and compliant automation solutions.Provide hands-on support for automated systems and equipment, ensuring optimal performance and reliability.Conduct solution assessments, performance evaluations, and system validations.Support the development and deployment of automation solutions, including replication of existing systems and implementation of new technologies.Manage engineering tools, and ensure adherence to standards, master specifications, and industry best practices.Offer technical coaching and consultation to engineering peers and contribute to continuous knowledge sharing.Assist in the integration of new equipment and technologies into existing manufacturing workflows.Key Qualifications: Bachelor's degree in Engineering (or equivalent industry experience)Minimum 5 years of experience in biopharma engineering, operations, or manufacturingAt least 5 years' experience in DeltaV control system design Strong understanding of instrumentation and control systems in a GMP-regulated environmentProven track record of technical leadership, problem-solving, and teamworkFamiliarity with GMPs, regulatory requirements, and computer system validation (CSV)Excellent communication skills, with the ability to convey complex technical concepts to both technical and non-technical stakeholders.