Equipment Engineering Roles (x3) – Biopharmaceutical Expansion Project, Dublin

Equipment Engineering Roles (x3) – Biopharmaceutical Expansion Project, Dublin

Overview

These roles will support a major biopharmaceutical manufacturing expansion project in Dublin, with primary responsibility for syringe filling and single-use formulation equipment. The positions will focus on equipment implementation, start-up, and ensuring full operational readiness in line with site and regulatory requirements.

Key Responsibilities

• As part of the site engineering team, support the expansion of an existing manufacturing facility, with a focus on syringe filling and single-use formulation equipment.

• Support manufacturing readiness activities, including start-up and validation of new systems and equipment, ensuring compliance with site standards and fit-for-purpose requirements.

• Assist with delivery of equipment project scope, including installation support, calibration, spare parts management, functional testing, start-up, and sustaining equipment in routine operation.

• Collaborate cross-functionally with Manufacturing, Quality, Process Development, Automation, IT/IS, EHSS, and Global Engineering stakeholders to ensure successful project execution.

• Establish maintenance strategies and develop initial preventive maintenance (PM) programs for new process equipment.

• Support vendor engagement and equipment supplier management throughout the project lifecycle.

• Travel as required to support project activities, including vendor or partner sites.

Basic Qualifications / Experience

• Bachelor’s degree in Engineering, with typically 5+ years’ experience in engineering projects and systems within regulated manufacturing environments.

• Strong working knowledge of applicable quality management systems and regulatory requirements (e.g. GMP).

• Experience supporting new technology introduction and equipment deployment within manufacturing facilities.

• Proven ability to analyse and resolve complex technical and operational issues.

• Manufacturing experience within a biopharmaceutical formulation and/or fill-finish facility.

• Strong technical documentation, communication, and stakeholder engagement skills.

• Experience working with equipment vendors and external suppliers.

• Self-directed, well-organised, and capable of managing multiple priorities in a fast-paced project environment.

• Demonstrated ability to work collaboratively across functions and levels to support effective decision-making and project delivery.