Live opening · Posted 5 days ago
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Job Summary
We are seeking an experienced LabVantage LIMS Consultant/Developer to join our team. The ideal candidate will have strong expertise in LabVantage LIMS 8.x or higher, laboratory system integrations, workflow development, and regulatory-compliant solutions for pharmaceutical, biotechnology, or manufacturing environments. This role involves configuring, customizing, supporting, and enhancing LabVantage LIMS while ensuring compliance with industry regulations and quality standards.
Key Responsibilities
Configure, customize, and maintain LabVantage LIMS to support business and laboratory operations.
Design and develop LabVantage workflows, specifications, and business processes.
Build and support laboratory instrument integrations and external interfaces, including ELN and third-party systems.
Perform data migration, system configuration, and application enhancements.
Develop and execute test scripts and validation documentation following SDLC and CSV methodologies.
Troubleshoot application issues and provide technical support to laboratory users.
Conduct end-user training and prepare support documentation.
Participate in system upgrades, patches, and deployment activities.
Collaborate with cross-functional teams to gather requirements and implement solutions.
Ensure compliance with GxP, FDA 21 CFR Part 11, and other applicable regulatory requirements.
Key Skills
LabVantage LIMS 8.x+
LIMS Configuration & Customization
Instrument Integration
ELN Integration
Java / JSP
SQL
JavaScript
Data Migration
CSV Validation
SDLC
GxP
FDA 21 CFR Part 11
Laboratory Informatics
Troubleshooting & Support
Requirements
Required Qualifications
Bachelor's or Master's degree in Computer Science, Life Sciences, Engineering, or a related discipline.
Hands-on experience with LabVantage LIMS 8.x or higher.
Strong understanding of LabVantage architecture, modules, administration, and configuration tools.
Experience with laboratory instrument integration and ELN interfaces.
Proficiency in Java, JSP, SQL, and JavaScript.
Experience with data migration, system validation, and testing activities.
Knowledge of Software Development Life Cycle (SDLC) and Computer System Validation (CSV).
Strong analytical and troubleshooting skills.
Excellent communication and stakeholder management skills.
Preferred Qualifications
Experience in pharmaceutical, biotechnology, or manufacturing laboratory environments.
Understanding of laboratory workflows and quality processes.
Knowledge of integration technologies, APIs, and web services.
Experience supporting regulated environments and validation projects.
Work arrangement
Hybrid
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