Operations Supervisor - Visual Inspection (Night Shift)
Company: Eli Lilly and Company
Location: Durham
Posted on: January 8, 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. Organization Overview: At
Lilly, we serve an extraordinary purpose. For more than 140 years,
we have worked tirelessly to discover medicines that make life
better. These discoveries start in Lilly Research Laboratories,
where our scientists work to create new medicines that will help
solve our world’s greatest health challenges. Lilly is designing
and building a new state of the art Parenteral, Device Assembly,
and Packaging Facility in Raleigh-Durham North Carolina. This is an
exciting opportunity to help build a state-of-the-art facility and
Quality System from the ground up. Responsibilities: This position
will start on an 8 hour, M-F schedule for onboarding, and is
expected to transition to a 12-hour, 2-2-3 rotating night schedule
within 2-3 weeks. The transition to night shift is a requirement of
this position. During the project phase, the Operations Supervisor
– Visual Inspection will support commissioning/qualification
activities required to bring automated and semiautomated inspection
lines into service, as well as supporting site operational
readiness activities. This role is expected to be an on-the-floor
leader and will be a subject matter expert for the visual
inspection process. This role may have the opportunity to be
directly involved with hiring team members. Concurrent with project
phase, the Operations Supervisor – Visual Inspection is responsible
for shift leadership for multiple drug product inspection lines
within the area, as well as developing technical expertise of
manufacturing employees. This individual must ensure that the
manufacturing lines are adequately staffed with trained/qualified
employees. Strict adherence to safety and quality rules and
procedures is required. This is direct line supervision for line
leaders and operators on a 12-hour shift rotation schedule. Key
Objectives Support Site Leadership to build a diverse, inclusive,
and capable site organization by delivering area operational
procedures, quality processes and controls for Parenteral areas
Responsible for hiring/managing 10 direct reports working across
multiple manufacturing lines Responsible for maintaining a safe
work environment, working safely, and accountable for supporting
all HSE goals Ensures qualified/trained staffing for operators
working on the manufacturing lines Communicate with the area
Manager on quality, equipment, and operational issues and areas for
improvement Responsible for the coaching, development, and
performance evaluation of operators/technicians
Originate/Investigate deviations or operational quality issues
Collaborate with support functions to achieve a consensus for
unexpected events during manufacturing Act as both administrator
and technical leader for operations, setting a good example through
demonstrated knowledge of procedures, compliance with quality
systems and use of proper technique Responsible for shop floor
execution as it relates to business plan and current Good
Manufacturing Practice (cGMP) conformance Basic Requirements: High
School Diploma or equivalent 2 years previous experience in
operations or directly supporting a pharmaceutical manufacturing
operation Demonstrated leadership experience with an emphasis on
respect for people Skills in providing/receiving feedback and
creating employee development plans Basic computer skills (desktop
software) are required Strong understanding of FDA guidelines and
cGMP requirements Excellent interpersonal, written and oral
communication skills Strong organizational skills and ability to
handle and prioritize multiple requests Strong technical aptitude
and ability to train and mentor others Ability to work overtime as
required Ability to travel Qualified candidates must be legally
authorized to be employed in the United States. Lilly does not
anticipate providing sponsorship for employment visa status (e.g.,
H-1B or TN status) for this employment position Additional
Skills/Preferences: Bachelor’s Degree in science, engineering, or
technical field Previous experience with automated, semiautomated,
and manual visual inspection processes/equipment Previous
experience in facility/area start-up environments Previous
experience with Manufacturing Execution Systems and electronic
batch release Experience with root cause analysis/technical writing
Organizational and motivational skills Knowledge of lean
manufacturing principles Additional Information: Position may
include short duration assignments in Indianapolis or
internationally to establish specific process knowledge, establish
global contacts, and provide production support Ability to wear
safety equipment (safety glasses, safety shoes, protective gloves
etc.) 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 - $51.83
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, Durham , Operations Supervisor - Visual Inspection (Night Shift), Science, Research & Development , Durham, North Carolina