Senior Scientist/Principal Scientist, Drug Product Development
Company: Eli Lilly and Company
Location: Indianapolis
Posted on: November 27, 2025
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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. Overview: The Lilly
Bioproduct Research and Development (BR&D) organization is
focused on the development and commercialization of parenteral
formulations of small molecules and large molecules such as
monoclonal antibodies, novel therapeutic proteins and peptides. The
organization is also committed to the development of genetic
medicines which includes active investments in oligonucleotide
development, nanomedicines for tissue specific targeting and other
gene delivery strategies. The drug product team is also investing
in building new platforms to support complex formulations such as
lipid nanoparticles (LNPs), antibody drug conjugates, AAV, and
other non-viral vector delivery vehicles. We are seeking a highly
motivated candidate for the position of Senior/Principal Scientist,
Biologics Drug Product Development, located in Lilly Technology
Center, Indianapolis Position Summary: This position is responsible
for conducting pre-formulation characterization, formulation of
parenteral and novel delivery systems, commercial development
studies and technology transfer to manufacturing sites for assigned
antibody-siRNA conjugate (ARC), co-formulation product and other
projects. The scientist will interact closely with other scientists
and may be an integral part of multidisciplinary teams that provide
support for product and process development as well as working with
Discovery, API development, Analytical Development, Delivery Device
and Connected Systems (DDCS), CT Operations and Manufacturing.
Responsibilities: Independently lead project, including
experimental design, execution, and efficient use of data to plan
next steps, ability to multi-task and collaborate effectively
across CMC functions and with medical, marketing, PK/PD, and
toxicology. Conduct studies to support any manufacture of supplies
for GLP studies and needed compatibility testing. Conduct
pre-formulation characterization and formulation studies to develop
clinical formulations. Provide support for successful manufacture
of clinical supplies. Good judgment and escalation of technical
issues and risks in a timely manner. Authorship of technical
reports and regulatory documents (IND/CTA, BLA/NDA). Present data
at deep dive, formulation and/or other technical forums.
Familiarity of CT and commercial platform processes, working
knowledge of CMO operations, as appropriate. Technology transfer of
formulation and/or manufacturing process as appropriate to sites
for CT and/or commercial manufacture. Work effectively with the
Bioprocess organization in the definition of the API matrix and in
the development of the formulated bulk. Work effectively with
Analytical Development in the definition of Drug Product physical
and chemical stability properties as well as coordination of
analytical testing support. Familiarity of API manufacturing
process and impact on drug product Critical Quality Attributes.
Conduct commercial development studies collaborating effectively
with functions such as Engineering, Statistics, Technical
Sciences/Manufacture Sciences and manufacturing sites. Keep abreast
of relevant new technologies / capabilities and regulatory
initiatives / requirements. Implement new capabilities, as
appropriate. Support organizational initiatives, as required. Work
effectively with external partners on outsourcing efforts and
research collaborations. Ensure work is aligned with all relevant
PR&D Development Quality, regulatory and HSE requirements. Good
laboratory skills and familiarity with formulation,
analytical/biophysical techniques and methods capability and
hands-on experience with laboratory instruments. Good communication
skills, ability to follow instructions and attention to details,
perform sample forecast, retrieve and compile data from appropriate
database. Basic Requirements : Master’s or Bachelor’s degree in
Pharmaceutical Sciences, Chemistry, Biochemistry, or a related
discipline, with 3–5 years of biopharmaceutical industry experience
in biologics formulation and process development. Strong background
in parenteral liquid and lyophilized formulation and
biologics-device combination product development, with deep
understanding of stability considerations for parenteral drug
products such as antibodies, peptides, and nucleic acid–based
therapeutics. Hands-on experience in the development of
antibody–siRNA conjugate (ARC) products is a plus. Proficiency with
standard computer applications and data analysis tools. Excellent
oral and written communication skills, with demonstrated ability to
collaborate effectively in cross-functional development teams.
Additional Preferences: Experience / knowledge of pharmaceutics,
chemistry, or biochemistry with understanding of parenteral dosage
forms and parenteral drug product stabilities. Additional
Information:? ? ?Located in Indianapolis, Indiana, Lilly Technology
Center – North 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 -
$193,600 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 , Senior Scientist/Principal Scientist, Drug Product Development, Science, Research & Development , Indianapolis, Indiana