Lilly Posted August 12, 2026

Associate Director – QA – LAPI

Lebanon, Indiana, United States of America FULL_TIME
Quality Associate 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 production of API molecules located in Lebanon, IN.  This facility is Lilly’s largest investment in manufacturing capacity and is intended to provide APIs for current and future products, including new modalities.  This is a unique opportunity to be a part of the site team for the startup of a greenfield 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 Brand Description:

The Associate Director – QA is a partner with the Sr. Director – QA in ensuring that operations have robust quality oversight. The Associate Director – QA is primarily responsible for the productivity and development of the QA employees, the quality of the product/results, oversight of manufacturing and support operations and overall customer service.  It is expected that the Associate Director will oversee the department’s performance, resolution of quality issues, and regulatory compliance.

Key Objectives/Deliverables:

Provide coaching/feedback to and develop QA employees.

Utilize Human Resources tools to ensure that the right individuals are in the right job (e.g., Performance Management, Merit Delivery, Talent Assessment, Succession Planning and Staffing).

Participate in organizational planning.

Provide input into the business plan and ensure conformance to department budget for area of responsibility.

Exhibit cross-functional influence.

Maintain and improve quality systems.

Approve deviations, procedures, protocols, and change controls.

Develop and maintain processes that support inspections and audits; prepare individuals to interact with auditors and inspectors.

Participate in self-assessments and regulatory agency inspections.

Ensure internal and external quality and supply commitments are met.

Provide quality management oversight for API manufacturing, laboratories, and warehouses.

Investigate complaints.

Manage the creation, revision, and maintenance of cGMP documents (e.g., job aids, procedures, forms, job descriptions).

Provide oversight and review of changes to the Global Quality Standards and ensure local implementation of changes.

Network with other sites regarding new or current quality systems.

Basic Requirements:

BS or equivalent in a scientific field or engineering.

5+ years in CGMP Manufacturing.

Additional Preferences:

Knowledge of cGMPs.

Experience in Manufacturing, QC, QA, Technical Services, Engineering or Regulatory Affairs Leadership

Previous experience supervising/leading people.

Demonstrated strong written and verbal communications skills.

Strong attention to detail.

Understanding of statistical tools and analysis.

Excellent interpersonal skills and networking skills.

Ability to organize and prioritize multiple tasks.

Demonstrated strong problem solving and analytical thinking skills.

Ability to influence diverse groups.

Demonstrated understanding of computer applications.

Other Information:

Must complete Learning Plan for Associate Director – QA – LAPI.

No certifications required.

Tasks require entering manufacturing and laboratory areas which require wearing appropriate PPE.

Must support 24 hour/day operations.

Some travel may be required.

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

$123,000 - $180,400

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
Quality
Therapeutic area
Not listed
Location
Lebanon, Indiana, 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 238 comparable Associate Director Quality roles across 55 biopharma companies.

238Comparable roles tracked
221Currently active
55Companies hiring similar roles
28Countries represented

Salary context

49 of 238 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 $123,000/yr – $180,400/yr
Peer group range $98,050 – $219,500 (median $159,000)

Where these roles are based

Top locations among the 238 comparable roles

United States106
India26
Ireland22
China16
Singapore15
Japan10

+ 22 more countries

Seniority mix

238 of 238 peers have a known seniority level

Manager116
Senior97
Associate Director25

Therapeutic area mix

0 of 238 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
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
Same function Same seniority Same country
60%similar
Novartis Durham, United States Associate Director
Same function Same seniority Same country
60%similar
Novartis Indianapolis, United States Associate Director
Same function Same seniority Same country
60%similar
Boehringer Ingelheim Ridgefield, Connecticut, United States Associate Director
Same function Same 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%
Associate Director, Quality Assurance Compliance
Gilead Sciences, Inc. · Foster City, United States · Associate Director
Function Therapeutic area Seniority Country
60%
QA Operations Head (Associate Director)
Novartis · Durham, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, Global Quality Risk Management
Biogen · Cambridge, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director - Quality Assurance - Device Assembly
Lilly · Pleasant Prairie, Wisconsin, United States of America · 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.