Labware LIMS Developer

Regeneron Ireland; Limerick; On-site; EUR 37,000 - 88,000; Full time

Job summary

Regeneron Ireland seeks a LabWare LIMS Developer to join the IOPS IT team in Limerick, onsite. You will configure LabWare master data, develop LIMS subroutines, and build interfaces with instruments and enterprise systems within a GxP-regulated environment.

You will write SQL queries, create Crystal Reports for Certificates of Analysis, and contribute to IQ/OQ/PQ validations, ensuring compliant system delivery across stakeholders in QC, QA, and Validation.

Qualifications

• 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 IQ/OQ/PQ protocols and test scripts.
• Experience with Crystal Reports for custom reports, labels and Certificates of Analysis.
• 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 changes with full traceability.
• Develop and maintain LIMS Basic subroutines and build interfaces between LabWare and instruments or enterprise systems (ERP, MES, ELN).
• Write and maintain SQL queries and stored procedures; develop Crystal Reports for labels and Certificates of Analysis.
• Document solutions using User Requirements, Detailed/Functional/Technical specs, configuration test plans, SOPs, and training materials.
• Author and execute IQ/OQ/PQ validation; ensure compliance through change control with Validation and QA.
• Administer LabWare LIMS including security, upgrades, and audit trails; support user and regulatory inspections.
• Train IT Applications team and end users; coordinate enhancements with business stakeholders.

Skills

LabWare LIMS

REST/SOAP APIs

SQL Databases

GxP / 21 CFR Part 11

Crystal Reports

Version control (SVN/Git)

XML/JSON handling

Education

BS/BA in Information Technology, Life Sciences, or a related field

Tools

LabWare LIMS

SQL

Crystal Reports

REST/SOAP APIs

XML/JSON

SVN/Git

Job description

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 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: Onsite

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
• Associate IT Developer: 0 - 2 years of relevant experience, preferably including LabWare LIMS
• IT Developer: 2+ years of relevant experience, preferably including LabWare LIMS
• Senior IT Developer: 5+ 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

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 partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Salary Range (annually) €37,000.00 - €88,400.00

Benefits

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits.

For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about on-site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

If you have any questions, please speak with your recruiter.

About Regeneron

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA-approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases. Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.