Eli Lilly and Company
Sr. Director - API Operations
Eli Lilly and Company, Glen Allen, Virginia, United States, 23060
Senior Director – API Operations
Join Eli Lilly and Company. Eli Lilly is a global healthcare leader headquartered in Indianapolis, Indiana. We discover and bring life‑changing medicines to those who need them, improve disease management, and give back to communities through philanthropy and volunteerism.
Lilly is constructing an advanced manufacturing facility for monoclonal antibodies, bioconjugates, and aseptic drug product manufacturing in Goochland County, Virginia. This facility will provide capacity for current and future products. This unique opportunity is part of the leadership team for the startup of a manufacturing site, and the successful candidate will help build the organization, the facility, and the culture to enable a successful startup into GMP manufacturing operations.
Position Overview As Senior Director, Operations, you will lead manufacturing operations—either monoclonal antibody DS production or ADC/aseptic drug product production—ensuring the organization has the capacity, capability, and leadership to deliver the site’s manufacturing plan. You will integrate cross‑functional support teams, foster a strong safety culture, and contribute to strategic direction, organizational development, and cross‑functional issue resolution as part of the Lilly Site Lead Team.
Responsibilities Pre-Startup and Startup Phase
Lead collaborative and energetic operational readiness and startup initiatives.
Build an organization with the capability, capacity, and culture to achieve high standards in safety, quality, and operational excellence.
Develop and implement site systems and processes, drawing on internal expertise and best practices.
Embed lean principles and a continuous improvement mindset across operations and support functions.
Act as the end‑user representative during project delivery—providing input on design, commissioning, and startup decisions to ensure alignment with project goals and long‑term strategy.
Post Startup
Develop and execute strategic and operational plans for Production Operations.
Contribute to the site’s medium‑ and long‑term strategic direction.
Ensure compliance with all applicable regulatory requirements.
Maintain robust control systems to manage operations, identify compliance risks, and take corrective action.
Lead cross‑functional teams to implement new product introductions and continuous improvement initiatives.
Develop future management and technical leaders for site and global roles.
Requirements
Bachelor’s degree in a relevant discipline.
10+ years of experience leading pharmaceutical operations.
Additional Preferences
Experience in API manufacturing and Process Safety Management.
Strong knowledge of cGMPs.
Proven ability to build effective relationships across all organizational levels.
Demonstrated success in leading projects from initiation to completion—on time, within budget, and to high performance standards.
Skilled in developing and managing high‑performing, engaged teams with a strong safety culture.
Lilly is dedicated to helping individuals with disabilities actively engage in the workforce. If you require accommodation to submit a resume, please complete the accommodation request form at https://careers.lilly.com/us/en/workplace-accommodation.
Lilly is 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.
Salary: $163,500 – $239,800 (annual). Full‑time equivalent employees eligible for company bonus and comprehensive benefits program including 401(k), pension, vacation, medical, dental, vision, and employee assistance program.
#WeAreLilly
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Lilly is constructing an advanced manufacturing facility for monoclonal antibodies, bioconjugates, and aseptic drug product manufacturing in Goochland County, Virginia. This facility will provide capacity for current and future products. This unique opportunity is part of the leadership team for the startup of a manufacturing site, and the successful candidate will help build the organization, the facility, and the culture to enable a successful startup into GMP manufacturing operations.
Position Overview As Senior Director, Operations, you will lead manufacturing operations—either monoclonal antibody DS production or ADC/aseptic drug product production—ensuring the organization has the capacity, capability, and leadership to deliver the site’s manufacturing plan. You will integrate cross‑functional support teams, foster a strong safety culture, and contribute to strategic direction, organizational development, and cross‑functional issue resolution as part of the Lilly Site Lead Team.
Responsibilities Pre-Startup and Startup Phase
Lead collaborative and energetic operational readiness and startup initiatives.
Build an organization with the capability, capacity, and culture to achieve high standards in safety, quality, and operational excellence.
Develop and implement site systems and processes, drawing on internal expertise and best practices.
Embed lean principles and a continuous improvement mindset across operations and support functions.
Act as the end‑user representative during project delivery—providing input on design, commissioning, and startup decisions to ensure alignment with project goals and long‑term strategy.
Post Startup
Develop and execute strategic and operational plans for Production Operations.
Contribute to the site’s medium‑ and long‑term strategic direction.
Ensure compliance with all applicable regulatory requirements.
Maintain robust control systems to manage operations, identify compliance risks, and take corrective action.
Lead cross‑functional teams to implement new product introductions and continuous improvement initiatives.
Develop future management and technical leaders for site and global roles.
Requirements
Bachelor’s degree in a relevant discipline.
10+ years of experience leading pharmaceutical operations.
Additional Preferences
Experience in API manufacturing and Process Safety Management.
Strong knowledge of cGMPs.
Proven ability to build effective relationships across all organizational levels.
Demonstrated success in leading projects from initiation to completion—on time, within budget, and to high performance standards.
Skilled in developing and managing high‑performing, engaged teams with a strong safety culture.
Lilly is dedicated to helping individuals with disabilities actively engage in the workforce. If you require accommodation to submit a resume, please complete the accommodation request form at https://careers.lilly.com/us/en/workplace-accommodation.
Lilly is 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.
Salary: $163,500 – $239,800 (annual). Full‑time equivalent employees eligible for company bonus and comprehensive benefits program including 401(k), pension, vacation, medical, dental, vision, and employee assistance program.
#WeAreLilly
#J-18808-Ljbffr