Lilly Posted July 30, 2026

Associate Director - Engineering

Indianapolis, Indiana, United States of America FULL_TIME
Manufacturing & CMC 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.

Organization Overview:

Lilly has been manufacturing life-changing medicines for over 150 years, and our Indianapolis Parenteral Manufacturing (IPM) site is at the center of that mission. We produce sterile injectable products in vial, cartridge, and pre-filled syringe formats, and the work done here reaches patients around the world.

As Engineering Leader for our Formulation, Filling, and Automated Inspection operations, you won't just manage equipment, you'll build the systems, culture, and talent that ensure every batch is safe, reliable, and right. This is a role for someone who leads from the floor and thinks at the system level.

We make medicines people depend on. The engineering that keeps those lines running, reliably, safely, every day, starts with leaders like you.

What You'll Own

People & Culture, Develop, coach, and build a team that's technically sharp and quality-obsessed.

Equipment Reliability, Keep critical manufacturing assets qualified, maintained, and performing at the highest standard.

Quality & Compliance, Drive GMP adherence and regulatory readiness across a 24/7 manufacturing environment.

Business Performance, Set and track objectives that tie directly to IPM's reliability and supply goals.

Day-to-Day Responsibilities

Mentor and develop engineers; recognize performance and grow capability across the organization

Translate site business plan priorities into actionable engineering objectives with clear ownership and milestones

Ensure all equipment is properly maintained, qualified, and positioned to reliably supply medicine to patients

Develop and enforce local processes and procedures in alignment with the FUME asset management system

Remove barriers, technical, organizational, or cultural, that limit team effectiveness

Staff your team with the talent and skills needed to meet evolving business needs

Serve as a technical authority and escalation point for complex engineering challenges

Champion safety and quality, not just as compliance requirements, but as cultural values

Minimum Requirements:

Bachelor's degree in Engineering

4+ years of relevant engineering experience

Additional Preferences:

Parenteral or sterile manufacturing background

Prior supervisory or leadership experience

GMP / OSHA regulatory knowledge

Strong problem-solving and analytical skills

Clear communicator at all levels

Proven track record in talent development

Additional Information:

Monday–Friday day schedule; off-hours support required as needed given 24/7 manufacturing operations

Occasional 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
Manufacturing & CMC
Therapeutic area
Not listed
Location
Indianapolis, Indiana, United States of America
Employment type
FULL_TIME

How this role compares

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

We currently track 459 comparable Associate Director Manufacturing & CMC roles across 66 biopharma companies.

459Comparable roles tracked
426Currently active
66Companies hiring similar roles
27Countries represented

Salary context

150 of 459 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
Lowest disclosed · Senior Scientist II – CMC Developmental Sciences · AbbVie $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · Associate Director Packaging Development · Gilead Sciences, Inc. $182,070/yr – $235,620/yr
Peer group range $0 – $208,845 (median $150,600)

Where these roles are based

Top locations among the 459 comparable roles

United States275
India67
Ireland18
Singapore14
China's Mainland11
Switzerland10

+ 21 more countries

Seniority mix

459 of 459 peers have a known seniority level

Senior251
Manager165
Associate Director43

Therapeutic area mix

0 of 459 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 Indianapolis, Indiana, United States of America Associate Director
Same function Same seniority Same country
60%similar
Merck Rahway, New Jersey, United States of America Associate Director
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Associate Director
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Associate Director
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Associate Director
Same function Same seniority Same country
60%similar
Novartis Watertown (Massachusetts), 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, CMC Project Management
Lilly · Indianapolis, Indiana, United States of America · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, CMC Portfolio Management
AbbVie · North Chicago, IL · Associate Director
Function Therapeutic area Seniority Country
60%
Assoc Director, Outsourced Manufacturing
Gilead Sciences, Inc. · Foster City, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, Master Production Planner
Gilead Sciences, Inc. · Foster City, 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.