LabVantage LIMS Specialist-Senior

Location: Pune

Employment Type: full-time

Job Details

LabVantage LIMS Specialist-Senior

What You’ll Do

As a Senior LabVantage LIMS Specialist you will:

• Configure LabVantage LIMS modules to support bioanalytical workflows, including assay development, plate results, sample management, stability, and analytical testing processes.
• Design, configure, and validate bioanalytical assay workflows within LabVantage, ensuring alignment with scientific requirements and regulated (GxP) environments.
• Develop and maintain Groovy-based scripts for workflow automation, business rules, calculations, instrument integration, and data transformation within LabVantage.
• Develop project documentation and conduct demos of configuration to clients
• Collaborate with scientists, QA/CSV teams, and IT to gather requirements, design technical solutions, and support system validation activities (URS, FRS, DS, IQ/OQ/PQ).
• Ensure configurations comply with 21 CFR Part 11 and other validation procedure
• Collaborate with a team of LIMS consultants working across various sites for the LIMS deployment

What We’re Looking For:

• 
  Over 4 years of direct, hands-on experience working with the LabVantage LIMS platform
• Strong experience configuring and customizing LabVantage LIMS to support laboratory workflows
• Proven ability to design, configure, and validate bioanalytical assay workflows within LabVantage
• Highly skilled in developing and maintaining Groovy-based scripts for workflow automation, business rules, calculations, instrument integrations, and data transformations
• Strong understanding of laboratory operations and end-to-end lab processes
• Expertise in developing comprehensive project documentation and delivering configuration demonstrations to clients
• Excellent attention to detail with strong analytical and problem-solving skills
• Effective communication and collaboration skills, with the ability to work across cross-functional teams and mentor junior team members
• Experience working in regulated environments such as pharmaceuticals, biotechnology, or food safety
• Strong knowledge of GxP, 21 CFR Part 11, and other applicable regulatory requirements
• Bachelor’s degree in Life Sciences, Information Technology, or a related discipline