Sr. Director - Manufacturing Operations

Reposted 11 Days Ago
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Richmond, VA, USA
In-Office
164K-240K Annually
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
The Senior Director leads manufacturing operations for API production, ensuring operational readiness, compliance, and cultural development during startup. The role includes developing strategic and operational plans and managing compliance risks post-startup.
Summary Generated by Built In

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 is currently constructing an advanced manufacturing facility for monoclonal antibodies, bioconjugates, and aseptic drug product manufacturing in Goochland County, Virginia. This facility is intended to provide capacity for current and future products.  This is a unique opportunity to be a part of the leadership team for the startup of a 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.    

Position Overview

The Senior Director, Operations is responsible for leading 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. This role also integrates cross-functional support teams and fosters a strong safety culture.

As a member of the Lilly Site Lead Team, the Senior Director contributes to strategic direction, organizational development, and cross-functional issue resolution.

During the project delivery and startup phase, the role will focus on:

  • Supporting facility delivery and operational readiness.
  • Building the manufacturing organization and leadership structure.
  • Developing and implementing GMP systems and processes.
  • Shaping site culture and ensuring alignment with long-term business goals. 

Responsibilities:

Pre-Startup and Startup Phase: 

  • Lead collaboratively and energetically across all aspects of operational readiness and startup.
  • 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 external 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 (e.g., safety, quality/cGMP, environmental, financial, legal, HR).
  • Ensure Production Flow and Process Teams meet Lilly’s Manufacturing Standards for Operational Excellence.
  • Maintain robust control systems to manage operations, identify compliance risks, and escalate issues appropriately.
  • Monitor site and business area performance and take corrective action as needed.
  • 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 operations within the pharmaceutical industry

Additional Preferences:

  • Experience in monoclonal antibodies, bioconjugates, and/or aseptic drug product manufacturing preferred.
  • Process Safety Management experience preferred.
  • Strong knowledge of cGMPs and their application in manufacturing operations.
  • Proven ability to build effective relationships across all organizational levels, including close collaboration with the Site Leadership Team.
  • 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 and team-oriented culture.

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

$163,500 - $239,800

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

Top Skills

Cgmps
Gmp Systems
Lean Principles
Performance Management
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The Company
HQ: Indianapolis, IN
39,451 Employees
Year Founded: 1876

What We Do

Eli Lilly and Company engages in the discovery, development, manufacture, and sale of products in pharmaceutical products business segment. For more than a century, we have stayed true to a core set of values – excellence, integrity, and respect for people – that guide us in all we do: discovering medicines that meet real needs, improving the understanding and management of disease, and giving back to communities through philanthropy and volunteerism.

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