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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

LabWare LIMS Developer

Enterprise ApplicationsConfirmed live in the last 24 hours
Full-timeLimerick, Ireland€37k - €88.4k /yrIn-person

About the Job

Requirements

  • A Bachelor of Science or Bachelor of Arts degree in Information Technology, Life Sciences, or a related field, or an equivalent combination of education and experience.
  • Relevant experience requirements depend on level: Associate IT Developer requires 0–2 years; IT Developer requires 2 or more years; Senior IT Developer requires 5 or more years. LabWare LIMS experience is preferred for each level.
  • Experience writing, debugging, and maintaining LIMS Basic subroutines for triggers, calculations, workflows, and custom events, and building and consuming REST/SOAP APIs and working with XML and JSON.
  • Strong SQL skills, including complex queries and stored procedures, using Oracle, SQL Server, or similar.
  • Working knowledge of GxP, GAMP 5, and FDA 21 CFR Part 11, and experience authoring and executing IQ/OQ/PQ protocols and test scripts.
  • Experience with version control software such as SVN or Git.

Responsibilities

  • 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.

Desired Qualifications

  • Experience with LabWare LIMS.
  • Experience with Crystal Reports for custom reports, labels, and Certificates of Analysis.
  • Familiarity with biological laboratory techniques.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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