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.
Senior Technical Engineer – LabVantage Master Data
The Senior Technical Engineer will be leading designing, building, and automating analytical test methods and associated data and specifications within LabVantage LIMS, and for developing or coordinating the development of instrument drivers and integrations that enable direct data capture into LIMS from laboratory instruments.
This role combines domain expertise in laboratory processes and analytical methods with technical leadership in LIMS MD configuration & Custom development. The incumbent will play a key role in advancing the organization's digital laboratory ecosystem, driving data integrity, automation, and compliance in GxP systems.
Key Responsibilities
What you'll be doing:
LabVantage MD Development & Build
- Develop the configuration, creation, and lifecycle management of analytical test methods in LabVantage LIMS (i.e. All interconnected MDs to support entire workflow for test method to work as per expectations).
- Implement test templates, specifications, and parameter lists ensuring standardization and scalability across products and sites.
- Define and maintain Test method metadata structures for automation (units, limits, calculations, result entry templates).
- Custom Script development for data transfer or verifications.
- Implement Test method versioning, review, and approval workflows in accordance with organisational data governance and validation policies.
- Partner with functional SMEs to ensure test methods adhering with GxP, ALCOA+, and analytical method validation principles.
- Build test scenarios/ documents and Test method templates.
Technical Maintenance and Master Data Support
- Triage, analyze and resolve issues through root cause analysis, harnessing both business and technical knowledge to minimize downtime.
- Develop and maintain scripts, business rules, and LabVantage SDK components to automate data processing and workflow activities.
- Enable service improvement through fixes of incidences.
- Support and analyze instrument integrations (e.g., Lab Application – Empower, Chromeleon, SmartLab, Darwin, Complex instruments) and maintain data exchange with ERP, ELN, QMS, EM and analytics systems.
Automation & Digital Integration
- Develop automation frameworks to reduce manual effort in test method setup and instrument data handling.
- Support initiatives for automated test method build from structured templates or upstream systems (ERP/PLM).
- Collaborate with analytics teams to make instrument and method data analytics-ready for dashboards and trending.
Governance, Validation & Documentation
- Support for versioned MD, and auditable as part of GxP compliance and following regulatory and Lilly IT quality standards (CSV-Computer System Validation).
- Create design documents, configuration specifications and technical SOPs for test method.
- Support QA in CSV, change control, and periodic review activities.
- Active participation in audits and ensure all automation components meet 21 CFR Part 11 and Annex 11 requirements.
- Prepare and maintain design specifications, configuration documentation, and validation test scripts for IQ/OQ/PQ activities along with installation procedures.
- Support change control, release management, ensuring compliance and stability in a multi-environment setup.
Leadership & Collaboration
- Strong 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.
- 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.
What You Should Bring
- Strong analytical and critical thinking.
- Technical proficiency in LIMS MD development & management.
- Understanding of analytical lab workflows and instruments.
- Excellent documentation and verbal communication.
- Ability to work across global teams (IT, Quality, Lab Operations).
- Strategic outlook to connect lab automation initiatives with enterprise digital goals.
Basic Qualifications and Experience Requirement
- Bachelor's or equivalent degree in Computer Science / Instrumentation / Chemical Engineering / Analytical Chemistry, or related field.
- 8+ years of experience in laboratory informatics, preferably in the pharma, biotech, or chemicals industry.
- 4+ years of hands-on experience configuring and deploying LabVantage LIMS Master Data (i.e. test methods, specifications, calculations, and workflows).
- Experience integrating LabVantage with chromatography and analytical instrument systems (Empower, Chromeleon, Microplate readers, etc.).
- Strong knowledge of GxP, 21 CFR Part 11, and data integrity principles (ALCOA+).
- Familiarity with ETL/middleware tools and system validation (CSV/SDLC) practices.
- Exposure to data analytics or digital lab transformation projects is a plus.
- Hands-on experience 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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