Automation Engineer (Rockwell)

NeoDyne is a leading engineering company specialising in industrial automation, digital manufacturing, and electrical engineering solutions. With a strong presence across multiple sectors, including Life Sciences, Food & Beverage, and Energy, NeoDyne delivers leading-edge solutions that drive efficiency, safety, and performance for its customers worldwide. With a team of 220+ skilled engineers, our expertise spans the entire project lifecycle, from design and implementation to commissioning and operations. From our offices in Ireland, the UK, Romania, and the US, we operate on a global scale, combining technical expertise with local delivery. We support customers across Europe, North America, and Asia, delivering tailored engineering services that drive long-term success.NeoDyne is seeking an experienced Automation Engineer to support one of our key client sites on a contract basis. The successful candidate will work closely with the NeoDyne team and play a critical role in delivering automation expertise across the Dublin based site.This role operates in a System Owner capacity, responsible for the day-to-day support, reliability, and continuous improvement of critical automation systems supporting Formulation, Fill / Finish, Lyophilisation, Inspection and Packaging operations within a GMP-regulated environment.ResponsibilitiesAct as System Owner for critical automation systems in a GMP manufacturing environmentOwn the lifecycle management of automation systems, including maintenance, upgrades, and validationProvide hands-on automation support to manufacturing during routine operations, shutdowns, and engineering activitiesLead and support troubleshooting, incident investigations, and root cause analysis for automation-related issuesManage Change Controls, Deviations, and CAPAs associated with automation systemsMaintain accurate system documentation, configuration control, and software versioningImplement CAPAs through software changes, configuration updates, and documentation revisionsReview existing system designs and recommend improvements aligned with modern automation and regulatory standardsSupport new product introductions, technology transfers, and system upgrades from an automation perspectiveWork closely with Operations, Engineering, Quality, and vendors to deliver automation improvementsSupport digitalisation and Industry 4.0 initiatives, including data integration and system connectivityPromote a strong safety and quality culture, ensuring adherence to GMP and EHS requirementsRequirementsDegree in Automation, Electrical, Computer, Chemical, Biotech Engineering, or related discipline5+ years’ experience in a pharmaceutical or biopharmaceutical manufacturing environmentStrong experience supporting automation systems in a live GMP manufacturing settingRockwell Automation expertise, including:, Allen-Bradley PLCs, FTView SCADAProven experience with system ownership, troubleshooting, and lifecycle managementExperience managing Change Controls, Deviations, and CAPAsGood working knowledge of GAMP lifecycle, GMP, and data integrity requirementsStrong communication skills and ability to work cross-functionallyDesired/Nice to HaveExperience with biopharmaceutical Formulation or Fill / Finish systemsExposure to Inspection or Packaging automationExperience with FTBatch / batch or recipe-driven systemsKnowledge of ISA-88 / ISA-95 standardsExperience with industrial networks (e.g. Ethernet/IP, ControlNet, DeviceNet, BACnet)Exposure to digitalisation / Industry 4.0 initiativesExperience supporting technology transfers or new product introductionsCharacteristicsWe look for candidates who Work well as part of a team.Have excellent problem solving and diagnostic skills.Can complete tasks independently, capable of self-learning.Can prioritise and coordinate work.Have excellent customer service, interpersonal, communication and organisational skills.Can multitask and work well under pressure.Are a strategic business thinker.What's on OfferCompetitive hourly rate based on experiencePaid overtime available, depending on project demandsFlexible working hours may be accommodated in line with project requirementsOpportunity to work on a high-profile biopharma site with a collaborative, technically strong teamChance to be part of NeoDyne’s network of engineering professionals, contributing to impactful automation solutions in the life sciences sectorNeoDyne Ltd is an equal opportunity employer, and all applications will be treated in strictest confidence. Applicants must hold a valid EU passport or have the legal right to work in Ireland (e.g. Stamp 4).#LI-JC1