Analytical Technical Research Advisor, Process Translation & Exec...
Eli Lilly and Company - Indianapolis, Indiana, us, 46262
Work at Eli Lilly and Company
Overview
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Overview
: Lilly recently announced a
$4.5 billion
investment to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing in
a single location
, the Medicine Foundry will allow Lilly to further develop innovative solutions to
optimize
manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact. In the Project Delivery Phase and Startup Phase of the project (2025 to 2028), roles will be fluid and dynamic as we
endeavor
to support the project delivery, build a new organization, develop and implement the necessary systems and business processes
required
to support GMP operations. This will require significant collaboration,
creativity
and resilience as the Lilly Medicine Foundry goes from design, to start-up, and to steady-state operations. The Analytical
Technical Research
Advisor
role
,
Process Translation & Execution
,
a
technical-track
position
,
seeks a collaborative,
inclusive,
and
energetic leader who will define and lead the
strategy to be employed for the
analytical workflows and testing strategies in the Process Translation & Execution
(PT/E)
laboratories.
This position will play a key role in the
technical transfer of
synthetic
(small molecules, synthetic peptides,
and
oligonucleotides
)
and
biological (monoclonal antibodies, bioconjugates, and other emerging therapeutic modalities)
drug substance processes
from CMC teams to t
he Lilly Medicine Foundry
. The Lilly Medicine Foundry
,
a state-of-the-art
facility,
will
utilize
the
latest in
automation to further the analytical capabilities including on-line in-process
control testing through material release a
nd on
-
going process
monitoring at the site. The
PT/E
Analytical group will consist of high-level scientists focused on the implementation of
new technologies
and
analytical process improvements. This position involves working
cross-functionally within the site and across the network to develop
strategic
functional capabilities and will
ensure
appropriate capacity
, capabilities and business processes are developed,
implemented
and sustained to deliver
the required information to the project teams
.
This position will be key to ensuring a strong safety culture and
establishing
a safety,
quality
and continuous improvement focused mindset within the organization. Responsibilities
: Drive implementation of technical solutions and analytical strategies to enable drug substance
production at the Lilly Medicine Foundry.
Provide technical
leadership
for
PT/E
analytical activities
to be
executed
at the Lilly Medicine Foundry
. Ensure methods are technically sound, well developed, and
fit
-
for
-
purpose
.
Demonstrate high learning agility and the ability to understand and exploit effective scientific concepts and methods across multiple subject areas (e.g., chemistry,
PAT, and
modeling and simulation).
Mentor and develop scientific staff. Ensure continued technical and professional growth of group members, encourage efforts towards excellence and knowledge sharing.
Plan and manage short-term and long-term development activities. Develop and/or review technical agendas and timelines for project work. Recommend resource allocation to
accomplish
projects according to plans, communicate progress and propose changes in timeline,
objectives
, or direction
.
Collaborate closely with organizations across development and manufacturing to deliver material and information for clinical trials and regulatory submissions
.
Welcome varied perspectives to create
new solutions
.
Ensure work and team activities are aligned with all relevant development quality, regulatory, HSE, GLP and GMP requirements.
Basic Requirements: Ph.D. in analytical, biophysical, biochemistry, molecular/cell biology, or related field with
5+ years
relevant pharmaceutical experience;
OR
B.S. or M.S. with 15+ years of experience
commensurate
with a Ph.D. chemist/biochemist
.
Demonstrated
expertise
leading analytical efforts in pharmaceutical product development and commercialization. Proven skills developing,
validating
, and transferring analytical methods
.
Fundamental knowledge of cGMP compliance requirements
and
cGMP experience
.
Additional Preferences: Experience with product
development
, including technical transfer of analytical methods into manufacturing operations
.
Demonstrated ability to drive and accept change.
Good interpersonal skills and a sustained tendency for collaboration
.
Demonstrated success in persuasion, influence, and negotiation.
Ability to prioritize multiple activities and manage ambiguity.
Must possess strong communication (oral, written), organizational, and leadership skills
.
Other Information: Initial location at Lilly Technology Center, Indianapolis
.
Permanent location at the new Lilly Medicine Foundry in Lebanon, Indiana
.
F
lexibility to work from Indianapolis
(or other Lilly
sites) may
be
required
throughout 2025 and 2026
.
Position requires
on
-site presence, 8-hour days, five days per week, with flexibility to support activities during shutdowns, weekends, etc.
0-10% travel
required
.
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 $121,500 - $198,000 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
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