Senior DeltaV Engineer

Senior DeltaV Engineer (Dublin)OverviewNeoDyne is a leading Irish and UK Industrial Automation and Electrical Engineering company. Our B2B customer base extends to over 300 companies with turnover predominantly from large multinationals in pharma, high-end food and beverage manufacturing and energy sectors. The company is 25 years old and employs over 200 talented automation, electrical and IT engineers across offices in Dublin, Cork, Galway, Waterford, and Chesterfield, UK.NeoDyne is seeking an experienced Senior DeltaV 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 site.We are looking for an experienced Senior DeltaV Engineer to support configuration and testing of recipe phases, equipment modules, control logic, and interlock schemes at a biologics manufacturing site. The role requires expertise in DeltaV, batch automation, and GMP environments.Key ResponsibilitiesConfigure DeltaV for batch recipes, phases, and equipment modules per functional design specifications.Develop and implement control logic and interlock schemes for safe and compliant operation.Perform software testing, simulation, and troubleshooting of DeltaV configurations.Execute Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), and commissioning support.Work with process engineers, automation teams, and validation personnel to ensure seamless integration.Support GMP documentation including URS, FDS, DDS, test scripts, and change controls.Assist in troubleshooting and optimizing DeltaV system performance.Experience & SkillsRequired4+ years of experience with DeltaV in a biopharmaceutical or life sciences environment.Strong understanding of batch processing, S88 standards, and GMP regulations.Hands-on experience in recipe configuration, equipment module programming, and control logic development.Experience with testing methodologies such as FAT, SAT, and commissioning.Ability to interpret P&IDs, process descriptions, and automation design documents.Excellent problem-solving skills and ability to work in a fast-paced environment.Strong written and verbal communication skills for documentation and collaboration.DesiredExperience with Emerson DeltaV v13+ or higher.Knowledge of 21 CFR Part 11 compliance and validation requirements for regulated industries.Familiarity with MES, and other automation systems in biotech manufacturing.Experience with historians, alarm management, and data analytics for process optimization.Prior work experience in large-scale biologics or pharmaceutical facilities. 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.