LIMS + Labware/LabVantage Consultant

Infosys; Bengaluru; Vor Ort; INR 1.200.000 - 2.000.000; Vollzeit

Zusammenfassung

Infosys is seeking experienced LIMS specialists in Bengaluru to configure, customize, and support LabWare, LabVantage, and STARLIMS systems across multiple labs. You will gather requirements from laboratory stakeholders and design robust workflows and reporting solutions that drive data integrity and efficiency.

Responsibilities include system validation, testing, and documentation, as well as integrating LIMS with ERP, MES, ELN, and CDS platforms.

Qualifikationen

• Experience with LabWare, LabVantage or STARLIMS LIMS platforms.
• Understanding of laboratory workflows and sample management.
• Exposure to data management, SQL concepts, and reporting.

Aufgaben

• Configure, customize, and support LIMS applications (LabWare, LabVantage, STARLIMS).
• Gather and analyze laboratory requirements from stakeholders.
• Develop workflows, sample lifecycle management, test management and reporting.
• Perform validation, testing and documentation activities.
• Integrate LIMS with ERP, MES, ELN, CDS and other systems.

Kenntnisse

LIMS configuration

LabWare

LabVantage

STARLIMS

SQL

Data management

SDLC

Testing & validation

Problem solving

Communication

Jobbeschreibung

Experience in LabWare LIMS / LabVantage LIMS / STARLIMS. Knowledge of laboratory workflows and sample management processes. Understanding of instrument integration and data management. Experience in SQL, database concepts, and report generation. Knowledge of SDLC, testing, and validation processes. Excellent problem-solving and communication skills.

Configure, customize, and support LIMS applications (LabWare, LabVantage, STARLIMS). Gather and analyze business requirements from laboratory stakeholders. Develop workflows, sample lifecycle management, test management, and reporting solutions. Perform system validation, testing, and documentation activities. Integrate LIMS with ERP, MES, ELN, CDS, and other enterprise systems. Support data migration, master data management, and system upgrades. Troubleshoot production issues and provide timely resolutions. Participate in user training and knowledge transfer activities. Ensure compliance with laboratory and regulatory standards.

Exposure to Pharmaceuticals, Biotechnology, Life Sciences, Chemicals, or Healthcare domains. Understanding of GxP, FDA 21 CFR Part 11, GMP, GLP compliance requirements. Experience with LIMS implementation, migration, or upgrade projects. Knowledge of cloud-based laboratory solutions.