Senior Director, Global Process Owner - Quality Risk Management
Company: Eli Lilly and Company
Location: Durham
Posted on: June 24, 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. About the job 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. Responsibilities The Senior Director, Global Process
Owner for Quality Risk Management, as a leader within the Global
Quality Systems team, will establish and maintain the global
quality system for Quality Risk Management. They will provide
strategic oversight and expertise for the global QRM process,
including Global Quality System standards, practices, business
processes, implementation tools and associated IT systems.
Additionally, the Global Process Owner will lead the QRM Community
of Practice, including Global Process Leads and Area Process
Owners. They will lead key global projects and priorities within
the Quality System. The Global Process Owner will consult with
Lilly manufacturing facilities, external supplier organization,
marketing affiliate quality operations, regulatory, research and
development and other functions to educate on the quality system,
and proactively ensure compliance of Lilly’s Quality Systems with
various country agency standards, industry trends and scientific
principles. Key Objectives/Deliverables The Senior Director, Global
Process Owner for Quality Risk Management is responsible to:
Establish and maintain the global quality system for QRM to drive
standardization globally. Own the Global Standards, Processes,
Practices, Trainings, and implementation tools and ensure they are
designed according to regulatory, industry and company
expectations. Provide governance, lead the implementations of
improvement initiatives and foster a robust compliance mindset.
Ensure processes are executed consistently across the organization
and monitor signals to drive continuous improvement. Act as the
leader and SME to ensure supporting IT applications and analytical
tools are configured and maintained to support the business needs
and facilitates accurate reporting and analytics. Define a common
set of global effectiveness and efficiency metrics to drive
end-to-end performance. Monitor performance metrics, report and
provide insights to inform decision making to drive further
improvements. Develop, lead, mentor and maintain a community of
cross-functional SMEs to collaborate on proposed improvements and
deepen the knowledge of the associated processes & tools. Actively
collaborate with enterprise-wide teams on standardized global
business processes. As the subject matter expert, ensure inspection
readiness, directly interact with Health Authorities during
inspections and draft responses to observations as needed. 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 related to Quality Risk Management. Own the global
risk log and global risk register, ensuring that key quality risks
across the enterprise are actively being mitigated. Support the
Quality Maturity Model initiatives by actively enhancing the
cultural mindset across the enterprise to integrate QRM principles
into routine processes. Basic Requirements: 10 years’ experience in
the pharmaceutical industry in GxP roles, with several years
Quality experience. 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 with diverse teams and influencing areas not under
direct control. Strong strategic thinking capability with a focus
on the ability to execute strategic decisions while balancing
conflicting priorities. Proficiency in addressing operational
challenges through structured approaches and innovative solutions.
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. Prior experience with common QRM tools,
how and when to apply them, and maintenance of a risk log or risk
register. Prior experience working in at least two of Clinical
Operations / Development, Pharmacovigilance, Product Research &
Development or Commercial Manufacturing preferred. Additional
Information: Available to travel (domestic and international) when
required. Fluent in English, additional languages are also
recommended. Role may be based at selected Lilly Locations in
Europe or the US. 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, Lynchburg , Senior Director, Global Process Owner - Quality Risk Management, Science, Research & Development , Durham, Virginia