SystemsPlus is hiring for LabVantage LIMS Specialist
Exp :: 2 yr +
Location :: Pune - KoregaonPark
Hybrid work model.
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 2 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
Drop CV here adwait.gaidhani@systems-plus.com
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