Supervisor – QA Incoming
Company: Eli Lilly and Company
Location: Durham
Posted on: July 13, 2025
|
|
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. Lilly has a new state of
the art Parenteral, Device, and Packaging Assembly Facility in
Raleigh-Durham North Carolina. The QA Supervisor –Incoming
Inspection is responsible for providing leadership to the Quality –
Incoming Inspection team. The QA Supervisor – Incoming will oversee
the incoming materials, including goods receipt, sampling, incoming
inspections/testing, and inbound/outbound shipping processes. Key
Objectives/Deliverables: Practices safety behaviors with proper PPE
and lifting techniques. Supports all HSE Corporate and Site Goals.
Manage the QA – Incoming team, consisting of 8-12 Quality
Specialists. Responsible for training and managing the QA –
Incoming team in: Performing incoming inspections (raw materials,
components, printed packaging materials, etc.) according to
priority. Documenting inspections in accordance with procedures and
specifications. Ensuring materials not meeting specifications are
quarantined, per local procedures. Sampling, inspecting, and
documenting results utilizing electronic systems (Darwin, SmartLab,
etc). When sampling a portion of the batch, ensure proper sampling
plan is followed. Working with the QC Lab to deliver samples and
receive results Performing ID testing of materials utilizing Raman
or NIR Spectroscopy. Maintaining retains and samples per local
procedures. Communicate with QA Disposition team to ensure
materials are released in a timely manner, as to not delay
production. Evaluating damaged materials found on inbound shipments
or within the warehouse and determine acceptability. Ensuring
storage condition is tracked, accurate, adjusted (as needed)
including evaluating temperature excursions on shipments received
at the warehouse. Assists in resolving issues on inbound shipments
(i.e.incorrect quantity or product, contamination, etc.). Performs
appropriate transactions in SAP to ensure system represents
appropriate status of material (QI, blocked, scrapped, etc.)
Provides additional Quality support to warehouse, as necessary. May
need to assist with performing department activities to ensure
materials are available for production. Responsible for ensuring
team is trained and training remains in compliance. Communicates
with Associate Director and Quality Representatives on quality
issues. Lead, mentor, and coach QA – Incoming team, Operations, and
support personnel on quality matters, while supporting and driving
the site Quality culture. Ensure regular presence in operational
areas to monitor GMP programs and quality systems. Work with
materials management group to initiate complaints/remarks to
supplier for materials not meeting Lilly expectations. May
participate in investigations regarding materials or service
complaints. Networks with the business and ensures all materials
are dispositioned in a timely manner to support production
schedule. Authors/revises SOPs, materials specifications, as
needed. Interacts with other quality functions including QA
Warehouse Supports material related Supplier Change Notification's
(SCN). Participates in/supports regulatory inspections, as needed.
Requirements (Education, Experience, Training): High school diploma
or GED Preferred attributes but not required: Previous materials or
warehouse experience. Previous experience leading and managing a
team. Demonstrated understanding of cGMP regulations related to QA
Inspection applications. Strong attention to detail. Proficient in
computer system applications. Ability to organize and prioritize
multiple tasks, highly flexible and able to work independently in
fast paced environment to support production demands. Excellent
interpersonal and networking skills. Highly motivated,
enthusiastic, share ideas and lead solutions effectively to
resolution; ensure safety of others. Understanding of statistical
tools and analysis. Experience in inventory management systems
(SAP, etc.) Previous experience in GMP production environments.
Previous facility or area start up experience. Other Information:
The position is for the Lilly Research Triangle Park site and will
support a 24/7 operation Ability to support off-shift requests
Ability to work 12 hour days – rotating 2-2-3 shifts. Ability to
work overtime as 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 $35.33 - $58.89
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, Lynchburg , Supervisor – QA Incoming, Science, Research & Development , Durham, Virginia