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Job Title


LabVantage LIMS Specialist


Company : Systems Plus


Location : Pune, Maharashtra


Created : 2026-03-07


Job Type : Full Time


Job Description

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 disciplineDrop CV here