Lilly Posted October 15, 2026

Associate Director - MQ IT

Huntsville, Alabama, United States of America FULL_TIME
Information Technology Associate Director
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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.

Overview

Lilly is investing more than $6 billion to create a new state-of-the-art manufacturing site in Huntsville, Alabama, the largest initial industrial investment in the state's history. The brand-new facility will utilize the latest technology for synthetic medicine Active Pharmaceutical Ingredient (API) manufacturing, producing small molecule synthetic and peptide medicines, to increase the company's manufacturing capacity. This is an exciting once-in-a-lifetime opportunity to help build and operate a new site.

The Lilly Huntsville site will be built using the latest high-tech equipment, advanced highly integrated and automated manufacturing systems, machine learning and AI, digitally integrated monitoring and advanced data analytics, and will have a focus on minimizing the impact to our environment. This is an opportunity you don't want to miss!

What You'll Be Doing

The Manufacturing & Quality (MQ) IT Associate Director – IT for the Huntsville Site will have responsibilities for different areas of the agenda like MES and Labs. This role will report to the Sr Director for Tech at Lilly MQ. They will ensure that the IT portfolio enhances the organizational strategy for the site through successful, consistent, and predictable delivery of programs, projects and applications that benefit the internal organizations and aligns with overall global IT strategy for Manufacturing, Quality, and Supply Chain.

Key Objectives/Deliverables:

Ensure site operational readiness from IT perspective. Site start up and integration of IT systems including: Manufacturing Execution System (MES)

Data historian, Real Time Floor Tracking

Data Integration

Data Integrity

Laboratory information management

Provide IT site functional leadership.

Implement site Digital Tech strategic and business plan.

Partner with the site capital project team and Global Facilities Delivery to ensure IT and OT requirements are embedded in facility design, construction, and commissioning.

Dynamically adapt road maps to site evolution/strategic directions, and new trends/issues.

Partners cross-functionally locally and globally to establish and implement site IT roadmap.

Responsible for maintaining a safe work environment.

Define and execute IT inspection readiness activities.

People

Ensure staffing to meet the site and functional agenda.

Lead, coach, and develop members of the team.

Support diversity, equity and inclusion in recruiting and development of team members.

Lead recognition, pay and promotion decisions.

Operational Excellence

Ensure IT organization is functionally strong and operationally focused.

Ensure solution focused organization.

Provide prioritization and barrier removal.

Provide oversight of technical activities within the group.

Effectively encourage knowledge sharing and education.

Basic Qualifications

Bachelor’s Degree in IT, Computer Science, Engineering

Minimum 7 years IT Technical Leadership experience working in Pharma and Manufacturing and Quality.

Preferences

Experience delivering IT for a greenfield capital project, including construction phase, commissioning and qualification, and site start up.

Experience with API small molecule and/or peptide manufacturing and the associated automation landscape.

Strong experience with MES system implementations, Data Integration and Advanced Analytics.

Regulatory compliance knowledge and experience (cGMP).

Demonstrated creativity, analytical thinking, and the ability to troubleshoot and solve problems.

Excellent written and oral communication skills.

Additional Information:

The role is Monday through Friday and based on-site. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hours and/or off-hour work may be required.

Position will be based out of Huntsville, Alabama, with ability to travel to Indianapolis and other Lilly sites as required.

The site is actively construction; the role may initially operate from temporary project facilities.

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

$132,000 - $193,600

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
Associate Director
Function
Information Technology
Therapeutic area
Not listed
Location
Huntsville, Alabama, United States of America
Employment type
FULL_TIME

How this role compares

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

We currently track 699 comparable Associate Director Information Technology roles across 66 biopharma companies.

699Comparable roles tracked
654Currently active
66Companies hiring similar roles
35Countries represented

Salary context

104 of 699 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 $132,000/yr – $193,600/yr
Highest disclosed · Senior Staff Engineer - DevSecOps · Exelixis Inc $219,000/yr – $311,000/yr
Peer group range $98,050 – $265,000 (median $180,500)

Where these roles are based

Top locations among the 699 comparable roles

India268
United States243
Spain35
Poland26
United Kingdom16
China14

+ 29 more countries

Seniority mix

699 of 699 peers have a known seniority level

Senior406
Manager204
Associate Director89

Therapeutic area mix

3 of 699 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology2
Vaccines & Infectious Disease1

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
Gilead Sciences, Inc. Raleigh, United States Associate Director
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
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60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Associate Director
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60%similar
Regeneron Pharmaceuticals, Inc (USA) Tarrytown, United States Associate Director
Same function Same seniority Same country

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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%
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Gilead Sciences, Inc. · Raleigh, United States · Associate Director
Function Therapeutic area Seniority Country
60%
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Gilead Sciences, Inc. · Foster City, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, Commercial Data Science
Amgen USA Inc. · Thousand Oaks, United States · Associate Director
Function Therapeutic area Seniority Country
60%
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Amgen Inc. · Remote, United States · Associate Director
Function Therapeutic area 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.