Supervisor - QC - IAPI
Company: Eli Lilly and Company
Location: Indianapolis
Posted on: February 13, 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. Position Brand
Description: The Leader – QC – IAPI provides leadership and
technical abilities to support the advancement of the laboratory
process knowledge/optimization, performance planning, and
compliance. The Leader – QC – IAPI also conducts an area’s daily
workload, contributes to laboratory testing, validation activities
and second person verification activities, and provides direction
and overall customer service while developing employees. Key
Objectives/Deliverables: Timeliness: Ensure work is completed in a
timely manner to support batch release and site priorities. Safety
and GMP Compliance : Adhere to Environmental Health and Safety
(EHS) requirements and laboratory safety procedures. Maintain
cleanliness and contamination control, in alignment with cGMPs,
chemical hygiene, and biosafety guidelines. Compliance and
Documentation : Execute activities in compliance with applicable
standard operating procedures (SOPs), methods/protocols, good
documentation practices (GDP), and regulatory guidelines. Data
Recording and Data Integrity : Execute activities in accordance
with data integrity standards and ALCOA principles. Data Review :
Perform data review, as assigned, to ensure accuracy and
compliance. Deviation Identification and Investigation : Identify
and escalate any atypical results and potential deviations.
Participate in root cause analysis for laboratory investigations
and implement corrective/preventive actions, as required. Provide
data to support manufacturing investigations, as required.
Continuous Improvement: Identify and communicate opportunities for
improvement. Cross-functional Participation : Participate in
cross-functional teams (e.g., process team, global working teams,
etc.), as required. Training and Mentorship : Maintain training
competencies and only execute work where qualified. Participate in
training and mentorship, as requested. Audit and Inspection Support
: Execute activities in a compliant manner that supports an ongoing
state of inspection readiness. Participate in pre-inspection
reviews/checks and provide on-site support during
audit/inspections, as requested Education Requirements: Associate's
degree (2-year College degree) in a science field related to the
laboratory in which they are placed (e.g., chemistry for chemistry
laboratory or micro or biology for micro laboratory) or 5 years of
demonstrated relevant experience in a GMP (analytical chemistry or
microbiology) laboratory. Basic Requirements: Requires in-depth
understanding of procedures and concepts in adjacent areas, as well
as expert technical knowledge in own work processes Responsible for
making decisions for own team; provides key input into decisions
impacting related teams or the local business area Influences
management on key decisions impacting the team; acts as a change
agent and influences others to understand, support, and drive
improvements Identifies and resolves day-to-day operational
problems in the team; solves complex problems in collaboration with
other team leaders; serves as a consultant when problems with
little or no precedent arise. Additional Preferences: Proficiency
with Electronic Laboratory Notebooks (ELNs-Smartlab, NuGenesis,
Labvantage), Laboratory Information Management Systems (LIMS -
e.g., Darwin, MODA, Labvantage), and Data Acquisitions
Systems/Equipment (Empower, Climets) Ability to work in a
laboratory environment, including wearing appropriate PPE and other
safety equipment and considerations. Ability to work in a highly
regulated environment. Demonstrated strong math and documentation
skills. Demonstrated strong oral and written communication and
interpersonal interaction skills. Previous laboratory experience.
Scheduling Experience Other Information: Must complete Learning
Plan for a Leader Supervisor – QC – IAPI. Schedule M-F (1300-2130)
On-call and holiday coverage may be needed to support direct
reports Overtime will be required to provide Leader/analyst
coverage for vacations/illnesses Must be able to lift at least 5
liters of liquid and carry equipment up flights of stairs. Tasks
may require repetitive motion and standing for long periods of
time. The job specification is intended to provide a general
overview of the job requirements at the time it was prepared. The
job requirements of any position may change over time and may
include additional responsibilities not specifically described in
the job specification. As always, you should consult with your
supervisor regarding your actual job responsibilities and any
related duties that may be required for the position. 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 $35.33 - $57.12
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, Fishers , Supervisor - QC - IAPI, Science, Research & Development , Indianapolis, Indiana