Sr. Director -QMS Operational Controls
Company: Eli Lilly and Company
Location: Indianapolis
Posted on: January 2, 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. Overview of Role: The
Senior Director, QMS Operational Controls will provide central
oversight of Operational Controls processes, ensuring alignment
with the greater Quality Management System (QMS) in terms of
strategy, infrastructure, and business tools. This role is
essential in maintaining the integrity and evolution of the process
framework by developing connections, standards, and governance to
support commercial and Clinical Supply functions. The incumbent is
accountable for health, management, and reporting across the
Operational Controls pillar of the QMS framework. This leader will
support excellence by aligning processes with business priorities,
ensuring compliance, and driving quality improvements. High-Level
Responsibilities: Lead Global Process Owners (GPOs) of
non-Quality-owned processes to deliver process excellence in the
Operational Controls Pillar of the QMS framework. Implement a
structured governance and monitoring model to deliver excellence
beyond Quality-owned processes across the framework. Design and
develop, in partnership with Management Review, a model for
determining the health of the QMS process ecosystem. Consult with
Lilly manufacturing, external supplier organizations, marketing
affiliate quality operations, research and development, and other
functions to educate on the quality system. Proactively ensure
compliance of Lilly’s Quality Systems with various country agency
standards, industry trends, and scientific principles. Ensure the
Global Standard, Processes, Practices, Trainings, and
implementation tools are implemented and maintained according to
regulatory, industry, and company expectations. Implement and
continuously improve governance that results in prioritization,
decisions at the right level, and enables QMS ease of execution for
required changes. Ensure processes are executed consistently across
the organization and monitor signals to drive continuous
improvement. Define a common set of global effectiveness and
efficiency measures to drive end-to-end QMS health, enable desired
performance, and build capability expertise. Partner with document
owners to obtain potential risks associated with document changes,
including regulatory non-compliance, process interruptions, or
misalignment between global entities. Develop strategies and
contingency plans to mitigate these risks. Monitor performance
metrics, report, and provide insights to inform decision-making to
drive further improvements. Develop, lead, mentor, and maintain the
GPO community to collaborate on proposed improvements and deepen
the knowledge of the associated processes and tools. Actively
collaborate with enterprise-wide teams on standardized global
business processes. Actively engage in external organizations and
industry organizations to monitor policy changes for
regulatory/external environments and advocate/influence
quality-related policies and regulatory requirements. Basic
Requirements: 10 years’ experience in the pharmaceutical industry
in business or quality operational roles across Research and
Development or commercial manufacturing. Bachelor’s degree in
Natural Science, Engineering, Pharmacy, or other Life
Science-related field. Additional Skills/Preferences: Proven
ability to work in a matrixed organization leading diverse teams
and influencing areas not under direct control. Experience leading
a major multi-site or global functions improvement initiative.
Strong strategic thinking capability with a focus on the ability to
execute strategic decisions while balancing conflicting priorities.
Ability to drive process improvements and strategic decisions by
analyzing and interpreting complex data. Demonstrated change
agility in anticipating and leading others through change and
ambiguity. Excellent teamwork, interpersonal, and communication
skills, with the ability to communicate and collaborate at all
levels through various formats. Expertise in developing scalable
and standardized processes across global operations to improve
efficiency and reduce complexity. Demonstrated influential
leadership expertise and experience engaging with senior-level
functional leads. Strong leadership capability to make and act on
decisions while balancing speed, quality, and risk to deliver
value-added business results. Strong capabilities in establishing
governance structures and proactively addressing quality and
regulatory risks. Demonstrated people management experience.
Expertise in navigating and ensuring adherence to global regulatory
standards and frameworks. Additional Information: Available to
travel (domestic and international) when required (ca. 10%). Fluent
in English; additional languages are also recommended. 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 $151,500 -
$222,200 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, Covington , Sr. Director -QMS Operational Controls, Science, Research & Development , Indianapolis, Kentucky