At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
About Lilly
At Lilly, everything we do starts with patients. We unite caring with discovery to make life better for people around the world. Headquartered in Indianapolis, Indiana, our global team of over 50,000 employees work with urgency and purpose to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. We bring our best to this work because people depend on it. If you're driven by purpose and determined to make a meaningful difference for patients, we invite you to bring your skill and your commitment to Lilly.
About Technology@Lilly
At Lilly, technology is not a support function. It is how a global medicine company operates, innovates, and delivers. Lilly in Hyderabad builds the capabilities that make this possible, cloud platforms, AI systems, and automation at enterprise scale, all in service of a purpose that makes this technology work genuinely distinctive, from advancing drug discovery to enabling connected clinical trials to keeping a global medicine company running at the standard patients deserve.
About the Business Function:
From molecule to market, Global Manufacturing plays an important role in every step along a product’s lifecycle. Most of our customers never see the scientific and technical resources behind our medicines. But customers experience, every day, the performance of our high-quality products and global supply network.
Global Manufacturing comprises a core group of functions that drives the production and supply of high-quality products: Engineering; Manufacturing Information & Control Systems Technology@Lilly Quality & Labs, Technology Services/Manufacturing Science; Global Health, Safety and Environment; and Supply Chain.
Junior LIMS Analyst
The Junior LIMS Analyst will assist in configuring LabVantage LIMS modules and provide foundational support to Quality Control (QC) laboratory operations. This role focuses maintaining Master data, system configuration, adhering to validation and GxP requirements, and supporting integrations between Lab and enterprise systems enabled with AI and automation.
Key Responsibilities
What you will be doing:
Master Data, Designs and System Integration
- Working with multi-functional teams to develop Master Data, create builds and participate in deployment.
- Implement test templates, specifications, and parameter lists ensuring standardization and scalability across products and sites.
- Partner with functional SMEs to ensure test methods adhering with GxP, ALCOA+, and analytical method validation principles.
- Ensures qualitative documentation of the processes and maintaining the artefacts.
Technical Development & Platform Support
- Provide L2 support for master data incidents.
- Participate in triage activities and assist with root cause analysis for problems/issues.
- Learn to develop simple scripts/business rules and use LabVantage SDK components with mentoring.
- Assist in solving instrument integrations and data exchange of LIMS with external systems.
- Follow release processes and maintaining version-controlled configuration and code.
Quality, Validation & Compliance
- Perform tasks in accordance with GxP, 21 CFR Part 11, and ALCOA++ data integrity principles.
- Assist in preparing design specifications, configuration documentation, and validation test scripts for IQ/OQ/PQ activities.
- Assist in change control, release management, and deployment activities to maintain validated state.
- Support for versioned Master Data, and auditable as part of GxP compliance and following regulatory and Lilly IT quality standards (CSV-Computer System Validation).
Master Data Support & Maintenance
- Analyze, triage, resolves L2 incidents and service requests; in developing knowledge base articles.
- Assist in service improvement through fixes of incidents.
- Identify small enhancements and process improvements; propose ideas to senior team members.
- Maintain reusable checklists and configuration artifacts to aid onboarding and scalability.
Collaboration & Learning
- Technical SME for LabVantage test method management.
- Collaboration with site-level LabVantage data stewards to lead test methods management.
- Partner with global digital, quality, and IT SMEs to define and implement standards for method and instrument onboarding.
- Enable process improvement through automation, template standardization, and adoption of new technologies.
How You Will Succeed
- Reduced manual effort and faster development of new test methods and incident management.
- Improved data flow between LabVantage and analytical instruments in secured environment.
- Compliance with global lab data governance and validation standards.
- Enablement of analytics-ready, high-quality laboratory data.
- Grow technical capability in scripting, automation, and integrations through mentorship.
What You Should Bring
- Excellent problem-solving and analytical skills with keen attention to detail.
- Willingness to learn, take feedback, and adopt new technologies/processes.
- Agile approach with focus on automation and enhancing with AI.
- Ability to work in teams and communicate clearly.
- Strong commitment to documentation and compliance.
Basic Qualifications and Experience Requirement
- Bachelor's or equivalent degree in Computer Science / Instrumentation / Chemical Engineering / Analytical Chemistry, or related field.
- 3+ years of experience in laboratory informatics, preferably in the pharma, biotech, or chemicals industry.
- 2+ years of hands-on experience configuring and deploying LabVantage LIMS Master Data (i.e. test methods, specifications, calculations, and workflows).
- Experience with LIMS or related laboratory/IT systems (internships or academic projects acceptable).
- Foundational understanding of lab workflows and compliance principles in pharma/life sciences.
- Interest in learning LabVantage configuration, scripting (Java/Groovy/SQL), and validation practices.
- Knowledge of GxP, 21 CFR Part 11, and data integrity principles (ALCOA+).
- Familiarity with system validation (CSV/SDLC) practices.
- Familiarity with JIRA, ALM, Git and ServiceNow (SNOW) for requirement tracking, defect management, and change control activities in regulated environments.
Additional Skills/Preferences
Certification in LabVantage Master Data and/or Stability, SDMS from LabVantage solutions is preferred.
At Lilly, caring is not only what we do for patients. It is how we work. We believe the people who dedicate themselves to making medicines better deserve an environment that makes their lives better too, one where they are supported, respected, and given the space to do their best work. This is not just a policy. It is who we are.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
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