LabVantage Developer

Ampstek; Bengaluru; On-site; INR 900,000 - 1,500,000; Full time

Job summary

Ampstek in Bengaluru, India seeks a LabVantage LIMS Specialist to configure, customize, and support LabVantage LIMS to meet business and laboratory needs. You will develop workflows, manage instrument interfaces, perform data migrations and validations, and provide end-user training.

Knowledge of GxP and FDA 21 CFR Part 11 is essential, with experience in pharma/biotech environments preferred.

Qualifications

• Bachelor’s or Master’s degree in Computer Science, Life Sciences, Engineering, or a related field.
• Strong knowledge of LabVantage architecture, modules, and administrative tools.
• Familiarity with Laboratory processes in pharmaceutical, biotech, or manufacturing environments.

Responsibilities

• Configure, customize, and support LabVantage LIMS to meet business and laboratory needs.
• Develop and maintain LabVantage workflows, specifications, and instrument interfaces.
• Perform data migration, test scripting, and validation activities (CSV/SDLC).
• Troubleshoot system issues and provide end-user support and training.
• Participate in LIMS upgrades and validation testing.
• Ensure compliance with GxP, FDA 21 CFR Part 11, and other regulatory standards.

Skills

Data migration

End-user support

Validation testing

Education

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

Tools

LabVantage LIMS

Job description

Exposure to Lab Instrument integration and ELN and Other interfaces.

Bachelor’s or Master’s degree in Computer Science, Life Sciences, Engineering, or a related field.

Strong knowledge of LabVantage architecture, modules, and administrative tools.

Familiarity with Laboratory processes in pharmaceutical, biotech, or manufacturing environments.

Configure, customize, and support LabVantage LIMS to meet business and laboratory needs.

Develop and maintain LabVantage workflows, specifications, and instrument interfaces.

Perform data migration, test scripting, and validation activities (CSV/SDLC).

Troubleshoot system issues and provide end-user support and training.

Participate in LIMS upgrades and validation testing.

Ensure compliance with GxP, FDA 21 CFR Part 11, and other regulatory standards.