We are recruiting Manufacturing Equipment Support Engineers for a leading global biopharmaceutical manufacturing company based in South Dublin.
The successful candidates will provide frontline engineering support within a highly regulated GMP manufacturing environment, ensuring production equipment operates safely, reliably and efficiently.
This is a hands-on engineering position focused on equipment troubleshooting, technical problem-solving, reliability improvements and supporting continuous manufacturing operations.
Key Responsibilities
- Provide frontline technical support to manufacturing operations, responding to equipment breakdowns and production issues.
- Troubleshoot mechanical and process equipment, identifying root causes and implementing effective solutions.
- Support preventative and corrective maintenance activities to improve equipment reliability and minimise downtime.
- Conduct root cause investigations and support corrective and preventative actions (CAPAs).
- Support GMP deviations, change controls and technical investigations.
- Identify and implement continuous improvement initiatives to enhance equipment performance and operational efficiency.
- Provide engineering support for manufacturing equipment, potentially including filling lines, formulation systems and associated process equipment.
- Support equipment modifications, commissioning and qualification activities where required.
- Work closely with Manufacturing, Maintenance, Quality and Engineering teams to resolve technical challenges.
- Ensure all engineering activities comply with GMP, safety and regulatory requirements.
Requirements
- Qualification in Mechanical, Process, Manufacturing, Chemical Engineering or a related discipline.
- Previous experience in equipment engineering, maintenance, manufacturing support or a similar technical role.
- Strong hands-on mechanical and process troubleshooting experience.
- Experience supporting manufacturing equipment within a regulated production environment.
- Knowledge of root cause analysis, preventative maintenance and equipment reliability.
- Understanding of GMP documentation, deviations and change control processes.
- Strong communication and problem-solving skills.
- Willingness to work a shift-based schedule.
- Experience in pharmaceutical, biopharmaceutical or medical device manufacturing.
- Exposure to sterile or aseptic manufacturing, including fill-finish operations.
- Experience with filling, formulation, packaging or other complex manufacturing equipment.
- Knowledge of equipment commissioning and qualification (IQ/OQ/PQ).
- Experience supporting investigations, CAPAs and continuous improvement initiatives.
- Familiarity with high-volume or continuous manufacturing operations.