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 manufacturing
- At least 5 years’ experience in DeltaV control system design
- Strong understanding of instrumentation and control systems in a GMP-regulated environment
- Proven track record of technical leadership, problem-solving, and teamwork
- Familiarity 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.