Labware LIMS Developer

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a LabWare LIMS Analyst/Developer to join our IOPS IT team, supporting the configuration, development, validation, and ongoing maintenance of LabWare LIMS and its interfaces to instruments and enterprise systems in a GxP-regulated environment. In this role, you will serve as a business-facing technical partner — developing custom solutions, managing master data, and ensuring compliant system delivery — while collaborating with QC, QA, Validation, and cross-functional laboratory stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & where: • Location: Limerick • Work model/flexibility: Onsit e Discover your role: • Configure and maintain LabWare master data including analyses, components, products, specifications, test methods, and sample plans; manage master data changes and migrations across environments with full traceability under change control • Develop and maintain LIMS Basic subroutines including triggers, calculations, workflows, and custom events; design, build, and support APIs and interfaces between LabWare and instruments or enterprise systems including ERP, MES, and ELN • Write and maintain SQL queries and stored procedures; develop custom reports using Crystal Reports including labels and Certificates of Analysis • Document solutions using standards and templates including User Requirement Specifications, Detailed Design Specifications, functional and technical specifications, configuration test plans, SOPs, and training materials • Author and execute validation protocols (IQ/OQ/PQ) for GxP and 21 CFR Part 11 compliance; process LIMS change control requests and partner with Validation and Quality to ensure systems follow the development lifecycle approach • Administer LabWare LIMS including security roles, upgrades, and documentation; participate in or lead security access reviews and periodic audit trail reviews • Troubleshoot issues, perform root cause analysis, and provide user support; provide application support before, during, and after regulatory and partner inspections • Train and mentor IT Applications team members and end users; coordinate with business stakeholders to gather, assess, and implement enhancement requests This role requires: • BS/BA in Information Technology, Life Sciences, or a related field • 2 years of relevant experience, preferably including LabWare LIMS • May consider equivalent combination of education and experience • Experience writing, debugging, and maintaining LIMS Basic subroutines for triggers, calculations, workflows, and custom events; experience building and consuming REST/SOAP APIs and working with XML and JSON • Strong SQL skills including complex queries and stored procedures (Oracle, SQL Server, or similar) • Working knowledge of GxP, GAMP 5, and FDA 21 CFR Part 11; experience authoring and executing IQ/OQ/PQ protocols and test scripts • Experience with Crystal Reports for custom reports, labels, and Certificates of Analysis preferred • Experience with version control software such as SVN or Git; familiarity with biological laboratory techniques a plus Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil