gLIMS Specialist

About the role

In this role, you will play a key part in safeguarding data integrity, optimizing gLIMS master data, and collaborating across global teams to support life-saving therapies. Working together in person supports close, real‑time collaboration and team alignment, enabling us to deliver our best work. You will work primarily in the office, with the flexibility to work remotely for 20% of your time (three days per week in office).

What you'll do

• Perform SOP-driven gLIMS master data tasks (creation, verification, approval, transfer) end-to-end to support global standards and business continuity
• Collaborate closely with the Global LIMS Office (GLO), local site representatives, and gLIMS/SAP IT teams for smooth execution of system configuration and testing
• Review master data requests from global sites for consistency with quality standards prior to approval
• Execute predefined validation test scripts, regression testing, and upload results for system changes and upgrades
• Prepare raw data extracts for QC KPI reporting and compile transactional data for periodic system reviews

What you need

• 5–9 yrs of experience
• SAP
• GMP
• Chemistry
• SOP writing
• Regression testing
• B.Tech or B.E. or MBA

Good to have

• MS Office
• Excel