LabVantage LIMS Specialist

SystemsPlus is hiring for LabVantage LIMS Specialist

Exp :: 2 yr +

Location :: Pune - KoregaonPark

Hybrid work model.

What Youll 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 Were 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

Bachelors degree in Life Sciences, Information Technology, or a related discipline

Drop CV here adwait.gaidhani@systems-plus.com