Principal Scientist, TSMS Small Molecule Synthesis - ADN RAMP Team
Location: Indianapolis
Posted on: June 23, 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. Position Brand
Description: The Lilly API/Dry Product Network is rapidly expanding
to meet the demand for new products, and several new greenfield
sites are under construction and will be starting up in the coming
years. The new sites are staffed based on full-scale, steady state
production, however additional surge capacity is needed to support
the site start-up and help quickly ramp to full capacity rates. The
ADN RAMP (Rapid Access to Medicines for Patients) team is a
cross-functional team that will bring deep manufacturing expertise
and will support each site start-up through Operational Excellence
knowledge, rapid troubleshooting and problem-solving capability,
and surge capacity resources. This unique opportunity will enable
team members to work at our new sites, create a larger Lilly
network, build and use their technical skills, and learn leadership
skills through formal training and on-the-ground experiences. This
team will also build strategies to help other new Lilly sites to
start up faster, helping to accelerate Lilly’s vision of serving
more patients. Success in this challenging role will require
supporting the sites through startup, through direct technical
execution, coaching next employees, and strong collaboration – and
development of the local technical and operational teams to be
ready for full operation. The team will directly report through
their respective functions but will be coordinated by the Ramp Team
Sr. Director. Key Responsibilities: Responsible for depth of Small
Molecule synthesis knowledge transfer and manufacturing support
during Small Molecule New Site Start-ups and process validation
execution. Key responsibilities include: Provide technical
leadership support to the new site TSMS team for technology
transfers from sending manufacturing sites or Development (internal
or external). Leverage prior experience to anticipate commercial
manufacturing challenges for new small molecule/synthetic active
pharmaceutical ingredients (APIs) through new site start-ups and
scale increases. Work with the local TSMS team to mitigate such
challenges. Work across the Development organization and
Manufacturing site(s) to implement appropriate product control
strategies based on anticipated needs of the new site. Establish
strong working relationships with Lilly’s Small Molecule
development organization (SMDD) to ensure development knowledge is
well established and available to support the new site tech
transfer. Establish depth of understanding of control strategy (CS)
of molecules being transferred and work with the site TSMS team to
translate this control strategy into unit operation requirements to
ensure robust and right first time technology transfer to new
facilities. Have a depth of understanding of the analytical control
strategy of the product being transferred that allows critical
technical review of the implementation of the analytical CS at the
new site, including process analytical technology for on line and
at line monitoring and control. Manage internal and external
relationships in cases where new manufacturing facilities are
receiving materials from External Manufacturing teams - providing
additional technical support/guidance for external manufacturing as
needed. Lead resolution of technical issues including those related
to control strategy and operational challenges at the site.
Collaboratively integrate different disciplines such as engineering
and analytical science on technical projects, process performance
improvements, or control strategy effectiveness. Provide proficient
data analysis and conclusions considering technical, Regulatory and
Quality compliance, and business needs. Work closely with
Development and Global Regulatory teams to author/review regulatory
submission documents and subsequently respond to Information
Requests/Regulatory Questions. Prepare, review, and approve study
designs, protocols, technical reports, and other related technical
documentation. Mentor and provide review/coaching to develop other
technical resources on scientific approach, technology, as well as
business approach and behaviors. Drive appropriate shared learning,
alignment and improvement across sites and network level activity
according to best practices and technical principles. Basic
Requirements: PhD or MSc in Chemistry or related science field with
5 years’ experience in pharmaceutical drug substance manufacturing.
Deep technical interest and understanding of product development
and manufacturing control strategy. Additional Skills/Preferences:
Excellent verbal and written communications skills. Strong
analytical and problem-solving skills. Collaborative skills with
operations, process engineering, QCL and other process team
members. Technical knowledge of manufacturing science. Ability to
coach others. Ability to influence without authority. Ability to
clarify and simplify complex issues. Strong trust building with
peers and leaders. Willing to work off-shift hours as needed to
support project milestones and training of new employees. Other
Information: The ADN RAMP team will support multiple new API/Dry
Products sites in various locations (US and OUS). Significant
travel may be required to current startup sites in order to meet
business needs, along with potential short-term assignments across
the network (can include international relocations). Candidates
must be mobile and flexible. 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 $64,500 -
$167,200 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: , Indianapolis , Principal Scientist, TSMS Small Molecule Synthesis - ADN RAMP Team, Manufacturing , Indianapolis, Indiana