Job Overview:
We are currently seeking a talented Utilities Engineer to join our team in Dublin. This exciting opportunity is perfect for someone who wants to leverage their technical expertise and passion for Utility Operations & Maintenance.
Key Responsibilities:
* Provide technical support on Utility Operations & Maintenance throughout the lifecycle of projects, ensuring key deliverables are achieved to support seamless handover to Operations.
* Develop 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 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, 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.
Qualifications, Skills, and Experience:
* A Bachelor's degree (Level 8) or Master's degree in a relevant Science or Engineering discipline.
* Experience 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.