Labware LIMS Developer

BioSpace; Ireland (WV); On-site; USD 42,000 - 99,000; Full time

Job summary

Regeneron in Limerick is seeking a LabWare LIMS Developer to join the IOPS IT team, supporting configuration, development, validation, and maintenance of LabWare LIMS and interfaces to instruments and enterprise systems in a GxP environment. You will partner with QC, QA, Validation and lab stakeholders to deliver compliant solutions and master data management.

Role requires working onsite with a strong focus on IQ/OQ/PQ validation, API design, and data integrity.

Qualifications

• BS/BA in Information Technology, Life Sciences or related field.
• 0-2 years: Associate IT Developer, LabWare LIMS preferred.
• 2+ years: IT Developer, LabWare LIMS preferred.
• 5+ years: Senior IT Developer, LabWare LIMS preferred.
• Experience writing and debugging LIMS Basic subroutines and APIs.
• Strong SQL skills and knowledge of GxP and 21 CFR Part 11.

Responsibilities

• Configure and maintain LabWare master data with full traceability under change control.
• Develop LIMS Basic subroutines, triggers, workflows, and interfaces to instruments and ERP/MES/ELN.
• Write SQL queries and create Crystal Reports for COAs and labels.
• Document designs and test plans per SOPs and design specs.
• Validate IQ/OQ/PQ protocols and support regulatory inspections.
• Administer LabWare LIMS security and change control; provide user support.

Skills

SQL skills

GxP knowledge

Validation knowledge

Problem solving

Communication

Education

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

Associate IT Developer

IT Developer

Senior IT Developer

Tools

LabWare LIMS

LIMS Basic

REST/SOAP APIs

XML/JSON

Crystal Reports

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.

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

Salary Range (annually)

37,000.00 - 88,400.00

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.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or 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/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

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 onsite. Please speak with your recruiter and hiring manager for more information about onsite 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.

For jobs in Canada: this posting is for an existing position.