Scientist – Quality Control Laboratory Informatics
At Lilly, we unite caring with discovery to make life better for people around the world. As a global healthcare leader headquartered in Indianapolis, Indiana, our employees worldwide work to discover and bring life‑changing medicines to those who need them, improve disease management, and give back to communities through philanthropy and volunteerism. We prioritize people and are looking for individuals determined to make life better for people worldwide.
The Scientist – QC Laboratory Informatics role supports laboratory operations by ensuring that electronic laboratory systems function as intended and comply with company and regulatory requirements. Initial responsibilities involve working with global and local IT support to populate master data, configure systems, and assist with installing and qualifying laboratory IT systems such as LabVantage LIMS, MODA, NuGenesis ELN, SDMS, Empower, and other laboratory systems. The role will evolve into monitoring, executing, and maintaining these systems with an emphasis on continuous improvement and data integrity. The position serves as the business representative for laboratory IT systems and mentors peers on system use and equipment, oversees management reviews, laboratory metrics, documentation, and supports internal and external audits as a subject‑matter expert.
Key Objectives / Deliverables
Validate laboratory equipment and software systems.
Maintain the validated state of software‑based computerized systems used in the laboratory.
Lead or support site deployment and upgrades of QC laboratory IT systems.
Ensure data integrity by design within the QC laboratory.
Act as QC laboratory data integrity local representative.
Build relationships with the Global Quality Laboratory Network and IT teams.
Serve as a contact SME for QC laboratory IT systems.
Perform non‑terminal record monitoring activities.
Support audit trail discrepancy resolution during system audit trail reviews.
Drive continuous improvement of quality systems in the QC laboratory.
Apply quality principles, cGMP, and laboratory systems knowledge to develop local procedures, training courses, and practices.
Create or revise worksheets, update documentation, and maintain method changes to improve quality systems.
Support audit and inspection activities for the laboratory.
Implement and comply with corporate, site, and laboratory safety standards.
Basic Qualifications
Bachelor’s degree in computer science, life science, applied science, or a related field.
Experience with IT systems installation, qualification, master data population, and configuration.
Experience in a GMP laboratory.
Minimum three years of relevant experience.
Additional Skills / Preferences
Master’s degree in a related field.
Proficiency with computer systems including Microsoft Office, LIMS, laboratory execution systems, chromatographic systems, and electronic laboratory notebook systems.
Experience operating or implementing laboratory IT systems such as LIMS and automated lab execution systems.
Experience with investigation and deviation management.
Proficiency in computer system validation.
Familiarity with compliance requirements and regulatory expectations.
Excellent oral and written communication; strong documentation and presentation skills.
Accurate analytical skills.
Ability to work in a laboratory environment with appropriate PPE and safety equipment.
Cross‑functional leadership experience utilizing problem‑solving and decision‑making skills.
Additional Information
Tasks may require repetitive motion and prolonged standing.
8‑hour workday, Monday through Friday.
May require support outside regular hours, including weekends or off‑hours, to support continuous 24/7 manufacturing operations.
Work will take place in various site areas. Some allergens are present in the parenteral plant; mobility requirements and allergen exposure should be considered.
Minimal travel required.
EEO & Accessibility Statement
Lilly is dedicated to helping individuals with disabilities actively engage in the workforce. If accommodation is needed for the application process, please complete the accommodation request form here .
Lilly is proud to be an EEO employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Compensation & Benefits
Actual compensation will depend on education, experience, skills, and geographic location. The anticipated wage range is $65,250 – $169,400. Full‑time employees are eligible for a company bonus (depending on performance). Lilly offers a comprehensive benefits program including 401(k) participation, pension, vacation and leave benefits, medical, dental, vision and prescription drug coverage, flexible benefits, life insurance, well‑being benefits, and employee assistance programs.