Were 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 sites 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.
Qualifications, Skills, and Experience: A Bachelors degree (Level 8) or Masters 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.
If interested in this posting please feel free to contact Sen McCarthy on or for further information.