Chemist - Quality Control

Company: Eli Lilly and Company
Location: Indianapolis
Posted on: November 27, 2025

Job Description:

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. Organization Overview: The Chemist – Quality Control in Indianapolis Radioligand Therapy (IRLT) group performs accurate and timely testing of routine and some non-routine radioactive lab samples in accordance with appropriate GMP and safety guidelines. The chemist completes second person verification of other's results. The chemist also participates in laboratory analytical investigations, equipment evaluations and qualifications, and some quality system improvement initiatives by executing well-defined protocols and procedures. The chemist shares technical information and best practice within plant sites or groups. Responsibilities: Sample Analysis and Reporting •Verify (SPV) analytical data of other analysts within the lab as requested. •Accurately and safely perform analytical test methods or related support activities as per procedures or protocols. Uses technical knowledge in the review and interpretation of data for conformances to procedures, standards, protocols, and/or real-time recognition of aberrant data and results. •Perform data entry and reviews own work for accuracy in accordance with laboratory procedures, standards and GMP requirements. •May perform holistic review of data for release of data from the laboratory. Problem Solving •Recognizes when a deviation from test methods and procedures has occurred and initiates analytical investigations and participates in a Root Cause Investigations. •Participates, including lead investigator duties, in investigations for deviations. •Assists in troubleshooting equipment and methods as required. Continuous Improvement Initiatives •Assist in improvement of quality systems by creating or revising worksheets and other lab documentation systems. •Identifies and communicates opportunities for improvement initiatives in daily work activities. •Reviews SOPs for executable as written. •Shares technical information and best practice within plant sites or group. Lab Operations •Assist with drafting protocols for non-routine testing or validation with appropriate guidance. •Assist in developing equipment qualification protocols with appropriate guidance. •Perform routine equipment calibrations or maintenance. •Comply with and assist with implementing safety standards. •Execute notification to management when required by procedures or standards. •Initiate lab deviations •Train and mentor others. Assist with developing training materials. Basic Requirements: •Bachelor’s degree in a science field related to the lab (e.g., chemistry, biochemistry, biology, etc.) •Preferred 1 years of experience in a GMP analytical lab Additional Skills/Preferences: •Experience with radioactive materials a plus. •Proficiency with computer systems LIMS, Empower, Chromeleon, Excel, etc. •Proficiency with UHPLC, pH meters, ICPMS, Rad detectors, Dose calibrators, and Gamma detectors, among others, a plus. •Ability to work in a lab environment, including wearing appropriate PPE and other safety required equipment and considerations. •Demonstrate strong math and documentation skills. •Demonstrate strong oral and written communication and interpersonal interaction skills. Additional Information: •Position supports a 4 day, 10 Hour shift (Saturday-Wednesday) or (Wednesday-Sunday) with both day and night shifts available. Night shift preferences will be considered favorably. •Tasks may require repetitive motion and standing for long periods of time. •Must be able to lift at least 5 liters of liquid. •Overtime work required, as necessary. Note: When applying internally for a position your current supervisor receives notification that you have applied to the position. We encourage employees to discuss the opportunity with their supervisor prior to applying. 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 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. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $148,500 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. WeAreLilly

Keywords: Eli Lilly and Company, Indianapolis , Chemist - Quality Control, Science, Research & Development , Indianapolis, Indiana