LabVantage LIMS Consultant / Developer

avacone Switzerland; Bengaluru; On-site; INR 1,800,000 - 3,200,000; Full time

Job summary

avacone Switzerland is seeking an experienced LabVantage LIMS Consultant/Developer to join our team in Bengaluru. The role focuses on configuring, customizing, and maintaining LabVantage LIMS, building workflows, and integrating instruments and ELN interfaces to support pharmaceutical, biotech, or manufacturing operations.

You will drive data migration, validation, and QA activities, ensuring alignment with SDLC and CSV methodologies while upholding GxP and FDA 21 CFR Part 11 standards.

Qualifications

• Hands-on experience with LabVantage LIMS 8.x or higher.
• Strong knowledge of LabVantage architecture, modules, and configuration tools.
• Experience with instrument integration and ELN interfaces.
• Proficiency in Java, JSP, SQL, and JavaScript.

Responsibilities

• Configure, customize, and maintain LabVantage LIMS to support operations.
• Design and develop LabVantage workflows, specifications, and business processes.
• Build and support instrument integrations and external interfaces, including ELN.
• Perform data migration, system configuration, and application enhancements.
• Develop and execute test scripts and validation documentation per SDLC/CSV.
• Troubleshoot issues and provide user support; conduct end-user training.
• 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 regulatory requirements.

Skills

LabVantage LIMS 8.x

LIMS config

Instrument integration

ELN integration

Java / JSP

SQL

JavaScript

Data migration

CSV validation

SDLC

GxP

FDA 21 CFR 11

Lab informatics

Troubleshooting

Education

Bachelor's or Master's in CS/Life Sciences/Engineering

Job description

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.