Lilly Posted June 28, 2026

Sr Director - HSE - GMP - Alabama

Huntsville, Alabama, United States of America FULL_TIME
Quality Senior Director

Lilly is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work, but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Lilly is currently constructing an advanced manufacturing facility for the production of API molecules. This facility is intended to provide APIs for current and future products, including new modalities.  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.

Main Purpose and Objectives of Position:

The Senior Director HSE is responsible for developing, implementing, and maintaining HSE programs and systems at the Lilly manufacturing site. This includes oversight of all site operations, manufacturing, labs, utilities, waste, emergency response, and administrative areas, ensuring compliance with global and regulatory standards.

This role leads the site HSE team, supports employee development, and serves as the primary liaison with corporate HSE to ensure alignment and readiness for regulatory inspections.

As a member of the Lilly Site Lead Team, the Senior Director contributes to strategic planning and cross-functional leadership. During the project delivery and startup phase (2029–2030), the role will focus on building HSE systems, processes, and culture to support GMP operations and enable a safe, compliant launch of full-scale manufacturing.

Key Responsibilities for this role include:

Pre-Startup and Startup Phase:

Lead collaboratively and inclusively across all aspects of operational readiness and startup.

Build an HSE organization with the capability, capacity, and culture to support safe, compliant, and efficient operations.

Define HSE priorities and roadmap; implement systems and processes using internal expertise and external best practices.

Establish and lead the site HSE Lead Team, embedding safety and environmental focus throughout project delivery and startup.

Serve as a key HSE stakeholder during project execution, guiding design, startup planning, and contractor safety in partnership with Global Facilities Delivery.

Develop and scale the HSE organization to support full GMP manufacturing, including environmental and PSM capabilities.

Build strong technical partnerships with corporate/global teams and lead site-level execution of strategic initiatives.

Post Startup:

Own the HSE Management System to ensure compliance with regulations and Lilly Global standards.

Define and manage HSE priorities, roadmap, business initiatives, metrics, and the HSE Plan in collaboration with functional partners.

Ensure ongoing compliance with reporting and recordkeeping requirements, including Title V.

Benchmark best practices across the Lilly network and external industry.

Develop future HSE leadership for both site and global roles.

Escalate critical HSE issues to site and corporate leadership as needed.

Requirements:

Bachelor’s Degree in relevant discipline

5+ years of experience leading HSE teams and programs (preferably with PSM and API manufacturing experience)

Additional Preferences:

Proven leadership of HSE programs and management systems in manufacturing, including Process Safety Management (PSM).

Experience implementing and managing environmental compliance programs, including Title V reporting and recordkeeping.

Skilled in engaging with regulatory agencies on environmental, health, and safety matters.

Strong ability to build effective relationships across all levels, including close collaboration with the Site Leadership Team.

Demonstrated success in developing high-performing, engaged teams and fostering a strong safety 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 (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

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

Job details

Seniority
Senior Director
Function
Quality
Therapeutic area
Not listed
Location
Huntsville, Alabama, United States of America
Employment type
FULL_TIME

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 31 comparable Senior Director Quality roles across 13 biopharma companies.

31Comparable roles tracked
24Currently active
13Companies hiring similar roles
10Countries represented

Salary context

14 of 31 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $163,500/yr – $239,800/yr
Lowest disclosed · Sr. Director - API Manufacturing Quality Assurance · Lilly $156,000/yr – $228,800/yr
Highest disclosed · Executive Director, QA Microbiology · Regeneron Pharmaceuticals, Inc (USA) $203,000/yr – $399,400/yr
Peer group range $192,400 – $301,200 (median $235,431)

Where these roles are based

Top locations among the 31 comparable roles

United States20
Ireland2
Singapore2
China1
Netherlands1
Canada1

+ 4 more countries

Seniority mix

31 of 31 peers have a known seniority level

Director24
Senior Director6
Executive/VP1

Therapeutic area mix

0 of 31 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Lilly Huntsville, Alabama, United States of America Senior Director
Same function Same seniority Same country
60%similar
Lilly Concord, North Carolina, United States of America Senior Director
Same function Same seniority Same country
60%similar
Lilly Huntsville, Alabama, United States of America Senior Director
Same function Same seniority Same country
60%similar
AstraZeneca Mt. Vernon, Indiana, United States of America Senior Director
Same function Same seniority Same country
50%similar
AbbVie North Chicago, IL Director
Same function Adjacent seniority Same country
50%similar
AbbVie North Chicago, IL Director
Same function Adjacent seniority Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Sr. Director - API Manufacturing Quality Assurance
Lilly · Huntsville, Alabama, United States of America · Senior Director
Function Therapeutic area Seniority Country
60%
Senior Director, Quality
AstraZeneca · Mt. Vernon, Indiana, United States of America · Senior Director
Function Therapeutic area Seniority Country
50%
Director, Study Quality and Compliance - Nonclinical Safety/Toxicology
Novartis · Cambridge (USA), United States · Director
Function Therapeutic area Adjacent seniority Country
50%
Director, QA Validation & Computer Systems Assurance
Regeneron Pharmaceuticals, Inc (USA) · Saratoga Springs, United States · Director
Function Therapeutic area Adjacent seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.