We’re currently recruiting for an exciting opportunity with a Biopharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.


Key Responsibilities:

• Provide technical expertise on Utility Operations & Maintenance throughout the lifecycle of projects, ensuring key deliverables are achieved to support seamless handover to Operations.
• Establish and maintain maintenance standards to drive safe and dependable operations through a focus on Reliability Excellence.
• Review vendor reports and documentation, ensuring timely and effective closure of Work Orders within the site’s CMMS (Computerized Maintenance Management System).
• Ensure that all Utility systems comply with applicable regulatory and legal requirements, including EPA licensing, GMP/cGDP standards, EHS policies, and Global Engineering and Construction directives and procedures.
• Collaborate with the Critical Utilities Operations and Maintenance team to optimize the performance and reliability of Critical Utility equipment. This includes enhancing plant operations, maintenance programs, SOPs, and risk assessments.
• Identify, diagnose, and resolve issues within Utility systems, applying effective solutions to minimize downtime.
• Oversee service delivery and nurture strong relationships with service providers, working in close coordination with internal stakeholders such as Operations, Maintenance, EHS, Quality, Procurement, and global functions.
• Participate in internal, external, and regulatory audits as required.

• A Bachelor’s degree (Level 8) or Master’s degree in a relevant Science or Engineering discipline.
• Eperience providing technical support in a live facility.
• Experience in operating and maintaining Utility systems within a biopharmaceutical manufacturing facility is preferred.
• In-depth knowledge of Utility system design, installation, maintenance, and troubleshooting, with the ability to interpret technical drawings and documents.
• Solid understanding of process design, GMP standards, maintenance practices, and relevant industry regulations within pharmaceutical manufacturing.