LabVantage LIMS Consultant / Developer

Posted 2 Days Ago
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Bengaluru, Bengaluru Urban, Karnataka, IND
In-Office
Mid level
Information Technology • Consulting • Pharmaceutical • Chemical
The Role
Configure, customize, and support LabVantage LIMS, including workflows, laboratory instrument integrations, ELN interfaces, data migration, testing, validation, upgrades, and troubleshooting. Develop Java, JSP, SQL, and JavaScript enhancements while following SDLC, CSV, GxP, and FDA 21 CFR Part 11 requirements. Collaborate with stakeholders, train laboratory users, and prepare technical and support documentation for regulated pharmaceutical, biotechnology, or manufacturing environments.
Summary Generated by Built In

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.

Skills Required

  • 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 and Computer System Validation
  • Strong analytical and troubleshooting skills
  • Excellent communication and stakeholder management skills
  • 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
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The Company
HQ: Sissach
66 Employees

What We Do

Avacone is a Swiss-based service provider specializing in IT infrastructure and pharmaceutical engineering, delivering specialized solutions for regulated and non-regulated environments in the pharmaceutical, chemical, and medical technology sectors.

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