Sr. Director - Program Commissioning and Qualification - Global Facilities Delivery
Location: Indianapolis
Posted on: June 23, 2025
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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. 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 35,000 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 is currently constructing an advanced manufacturing
facility for production of API molecules located in Lebanon, IN.
This facility is Lilly’s largest investment in manufacturing
capacity and is intended to provide APIs for current and future
products. This is a unique opportunity to be a part of the
leadership team for the startup of a greenfield manufacturing site,
and the successful candidate will help to build the organization,
the facility and the culture to enable a successful startup into
GMP manufacturing operations. Job Summary: The Program
Commissioning and Qualification Sr. Director will be responsible
for leading the commissioning and qualification (C&Q)
activities for major greenfield site capital projects within the
Global Facilities Delivery Projects team. This role involves
ensuring that all systems and equipment are properly commissioned
and qualified to meet regulatory and business requirements. The
lead will work closely with project managers, engineering teams,
and site operational readiness to deliver high-quality C&Q
programs. Key Responsibilities: Lead the development of an
effective safety programs from procedure development to execution
in the field during project C&Q. Develop and implement
comprehensive C&Q strategies for major capital projects,
including parallel commissioning of multiple production facilities
and support buildings in a GMP and process safety regulated
environment. Manage the development of CQ strategies and execution
plans, schedule, and budget to ensure timely and cost-effective
delivery. Provide technical oversight and guidance to the C&Q
team, ensuring adherence to industry standards and best practices.
Coordinate with project managers and teams to assess, provide
direction, and oversee the implementation of engineering and
construction services. Ensure all commissioning packages are
approved according to the trace matrix Develop and maintain
traceability matrices to demonstrate how commissioning testing met
user requirements. Develop project C&Q organization to support
schedule and deliver to budget in collaboration with the Process
Equipment COE and other key professional services to maintain a
diverse and capable pool of service providers. Monitor and
understand market conditions to educate and influence project
decisions with current data. Qualifications: Bachelor's degree in
Engineering, related science or Project Management, or a related
field. Minimum of 15 years of experience in commissioning and
qualification activities within the pharmaceutical or biotech
industry. Proven track record of managing large-scale C&Q
programs from design phase through to closeout and handover. Strong
knowledge of ASTM E2500 Model and Verification methodology.
Preferred Qualifications: Excellent leadership, communication, and
organizational skills. Ability to work effectively in a
cross-functional team environment. Experience with greenfield site
projects and pharmaceutical & process safety processes. Familiarity
with regulatory requirements and industry standards for
commissioning and qualification. Certification in project
management (PMP or equivalent) is a plus. Work Environment: Regular
collaboration with project managers, engineering teams, and quality
assurance 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 $147,000 -
$215,600 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: , Indianapolis , Sr. Director - Program Commissioning and Qualification - Global Facilities Delivery, Manufacturing , Indianapolis, Indiana