This role is responsible to
ensure efficient, compliant and scalable execution of global LIMS (gLIMS) operational activities. The gLIMS Support & Data Expert acts as an offshore execution specialist, performing SOP-driven master data, validation, and documentation activities to support business continuity, data integrity, and audit readiness across Lonza QC operations.
The role works closely with the Global LIMS Office (GLO), local site representatives, QA and IT partners to deliver accurate and timely outputs while maintaining global standards.
What You Will Get
Opportunity to work in a
global life sciences organization
with high regulatory and quality standards
Hands-on exposure to
gLIMS (LabVantage)
operations in a regulated QC environment
Collaboration with
global and local cross-functional teams
(QC, QA, IT, SAP)
A role with clear
ownership, structured processes, and defined accountabilities
Platform to contribute to
data quality, compliance, and system improvement initiatives
What You Will Do
Execute
SOP-driven master data activities
end-to-end (creation, verification, approval and transfer) as assigned by the Global LIMS Office or site representatives
Review master data requests from sites to ensure
consistency with global standards
Prepare raw data extracts and compile transactional data for
KPI reporting and periodic system reviews
Execute
predefined validation and regression test scripts
and upload results for system changes and upgrades
Upload approved validation, change and compliance documentation in line with
change management SOPs
Support periodic reviews of gLIMS data and processes to ensure
accuracy, compliance and audit readiness
Assist with
emergency or urgent changes
by executing scripted tests and providing required documentation
Collaborate closely with
GLO, LLO, QA and IT teams
to ensure smooth configuration and validation execution




Escalate unclear instructions, data inconsistencies or system issues promptly for resolution
What We Are Looking For
Bachelor's degree (or equivalent)
in a scientific or technical discipline (e.g. IT, Chemistry, Life Sciences)
5+ years of experience
in QC operations, LIMS support or digital laboratory systems within a regulated environment
Hands-on experience with
LIMS (LabVantage preferred)
and laboratory workflows
Experience with
CSV activities
, including execution of test scripts
Solid understanding of
GMP, data integrity principles, and compliance requirements
Solid attention to detail with the ability to execute structured, repeatable processes
Good understanding of
regulated QC laboratory operations
and typical gLIMS use cases
High accuracy in
master data management and documentation handling
Proficiency with
MS Office tools
(Excel, Word, Outlook); exposure to SAP, TrackWise or KNEAT is a plus
Structured, customer-oriented mindset with the ability to follow SOPs precisely
Ability to organize workload, manage priorities, and deliver
on time and to quality
Collaborative team player who communicates professionally across cultures and functions
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

📌 Glims Specialist (India)
🏢 Lonza
📍 India