Sr. LabVantage LIMS Architect

Overview

Remote
Depends on Experience
Contract - Independent
Contract - W2
Contract - 3 Month(s)

Skills

GxP
Development Testing
ELN
LIMS
Life Sciences
MES
OQ
Oracle
PQ
SOAP
IQ
Groovy
Enterprise Resource Planning
SQL
Scripting
Documentation

Job Details

Role: Sr. LabVantage LIMS Architect
Location: Remote
Type: Contract
Length: 3 months to start + Likely Extensions


we are seeking an experienced LabVantage LIMS Architect to lead the design, configuration, and implementation of LabVantage Laboratory Information Management Systems (LIMS). The ideal candidate will possess deep technical expertise in LabVantage, a strong understanding of laboratory workflows, and a proven ability to align LIMS capabilities with business and regulatory requirements.
Key Responsibilities:

  • Serve as the technical lead and subject matter expert (SME) for the LabVantage LIMS platform.
  • Architect and design scalable, secure, and high-performing LabVantage LIMS solutions tailored to business and laboratory requirements.
  • Lead end-to-end LIMS implementation and upgrade projects including requirements gathering, solution design, development, testing, deployment, and support.
  • Collaborate with cross-functional teams including QA, R&D, IT, and regulatory affairs to define user needs and ensure compliance with regulatory standards (e.g., FDA 21 CFR Part 11, GxP).
  • Develop and maintain system documentation including design specifications, configuration guides, and validation protocols.
  • Integrate LabVantage with other enterprise systems (e.g., ERP, MES, CDS, ELN).
  • Stay current on LabVantage product releases and new features to propose adoption strategies where beneficial.

Qualifications:

  • Bachelor's or Master's degree in Computer Science, Life Sciences, Engineering, or related field.
  • 6+ years of experience with LabVantage LIMS, including system architecture, configuration, scripting (e.g., Groovy), and database (Oracle/MS SQL).
  • Strong understanding of laboratory workflows and processes in regulated environments.
  • Experience with GxP, 21 CFR Part 11, and validation documentation (IQ/OQ/PQ).
  • Hands-on experience with system integration, web services (SOAP/REST), and interfacing instruments or other lab systems.
  • Excellent analytical, communication, and project management skills.
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