Scientist - Analytical Method Development SMDD Foundry Readiness
About The Position
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. Synthetic Molecule Design and Development has an exciting opportunity for an analytical chemist to join our development group. In this hands-on laboratory role (>70% bench work), you will develop analytical methods and characterize chemical processes to advance drug candidates from early development through manufacturing readiness. You will expand and apply your expertise in chromatographic method development and leverage complementary techniques (mass spectrometry, NMR) while partnering closely with synthetic chemists and process engineers to solve critical process development challenges. The ideal candidate brings practical chromatography experience, strong problem-solving skills, and the ability to translate analytical data into actionable insights for project teams.
Requirements
- Bachelor’s degree in Analytical Chemistry, Biochemistry, Chemistry, or a related field with 2+ years of relevant experience
Nice To Haves
- Experience with chromatographic (LC, GC, IC) method development or validation in pharmaceutical, chemical, or regulated industry setting
- Working knowledge of mass spectrometry (LC-MS, GC-MS) and NMR spectroscopy
- Familiarity with chemical process development, synthetic organic chemistry, and rationales for establishing material specifications and testing plans.
- Experience troubleshooting and maintaining analytical instrumentation.
- Demonstration of scientific leadership and the ability to influence others.
- Ability to balance multiple responsibilities, prioritize activities, and navigate ambiguity.
Responsibilities
- Develop and optimize analytical methods to accurately measure purity, potency, and other critical quality attributes of small molecule drug substances and synthetic intermediates.
- Select and implement appropriate analytical techniques (HPLC, GC, NMR, MS) to support chemical process development—independently generating data that elucidates reaction mechanisms, characterizes kinetic behavior, and identifies process-related impurities.
- Collaborate with synthetic chemists and process engineers to ensure analytical methods are suitable for guiding development activities and can be successfully transferred to GMP laboratories for routine testing and manufacturing support.
- Perform laboratory activities with a strong emphasis on safety and technical rigor, while adhering to local policies and procedures.
- Identify and apply new scientific concepts, exhibit strong problem-solving skills, and be self-motivated to contribute across multiple projects.
- Demonstrate strong written and verbal communication skills to represent both the technical aspects and business-related implications of your work.
Benefits
- Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).
- 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).
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
