LabVantage LIMS Specialist

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