Sr. Director - Manufacturing Operations

Senior Director, Operations

Position Overview

This senior director 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. The 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.
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 elevate 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.
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.
Compensation

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). Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.
Benefits

Company-sponsored 401(k) and pension
Vacation benefits
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
Time off and leave of absence benefits
Well‑being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
EEO Statement

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.

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