IDM TS/MS Product Steward (R2-R3)
Company: Eli Lilly and Company
Location: Indianapolis
Posted on: April 1, 2026
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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. Eli Lilly and Company
seeks an IDM TS/MS Product Steward (R2-R3) to develop potential
product and process improvements. Responsible for design control,
validation and verification activities, and manufacturing control
strategy. Develop specifications, protocols, sampling plans,
engineering studies, and technical reports. Provide support to
product lifecycle management and monitoring processes. Organize and
facilitate Failure Modes, and Effects Analysis (FMEA) meetings and
lead on multi-functional project teams. Lead root cause
investigation team to develop and implement corrective and
preventative actions. Participate in and support CMO Joint Process
Teams to meet manufacturing objectives. Participate in Design and
Manufacturability reviews. LI-DNI Position requires a Bachelor’s
degree in Mechanical Engineering, Biomedical Engineering,
Electrical Engineering, or a related engineering field and 3 years
of experience working in technical services/manufacturing sciences,
engineering, quality, development, or manufacturing/packaging in a
regulated manufacturing operations environment. Experience must
include a minimum of: 3 years of experience working with CAD
software packages (Solidworks, ProE, Inventor) and GD&T drawing
practices; 3 years of experience driving continuous improvement of
test systems and validation processes; 3 years of experience
leading analytical evaluations of events and deviations associated
with products, test systems, and analytical methods; 3 years of
experience working with device platforms, including design,
materials of constructions, manufacturing process, and quality
systems; 3 years of experience working with Primary Loop,
Operational Excellence, and Root Cause Analysis; and 3 years of
experience working with drug product and medical device regulatory
requirements, including cGMP, 21 CFR 820,ISO 13485, and ISO11608.
Up to 10% domestic and international travel required. LI-DNI Job
location: Indianapolis, IN. To apply, please visit
https://jobsearch.lilly.com/ and enter job requisition number
R-103503 when prompted. Alternatively, please send your resume,
cover letter, and a copy of the ad to: Matthew Tenaglio, Lilly
Corporate Center, Indianapolis, IN 46285. 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 $101,254.00 per
year 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, Carmel , IDM TS/MS Product Steward (R2-R3), Engineering , Indianapolis, Indiana
