Lilly Posted August 9, 2026

Engineer - Process Automation / IDAP Site Expansion - Assembly

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

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

At Lilly, we serve an extraordinary purpose.   We make a difference for people   around the glob e   by discovering,   developing   and delivering medicines that help   them   live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.

Position Brand Description

The Engineer – Process Automation will be a part of the IDAP Expansion Team, a dedicated team responsible for executing strategies and objectives to ensure successful delivery and ramp up of multiple assets within IDAP.  The Process Automation Engineer is the area expert for the automation systems, controls and integration aspects of the equipment they are assigned.  The Engineer – Process Automation is responsible for understanding all automation aspects of the asset delivery requirements within IDAP, partnering with the asset delivery organization SMEs (e.g. IDM/GPR), IDAP Site automation and infrastructure for ensuring the equipment is delivered, qualified and is capable of meeting customer needs.  The Process Automation Engineer will support the ramp up and handover to the process team after defined milestones.

Responsibilities

Safety

Ensure a safe working environment by enforcing and following HSE policies and ergonomic environment within process team.

Actively participate in safety-related activities (audits, JSA’s, hazard reviews, etc.) to drive ongoing safety improvement.

Wear proper personal protective equipment (gloves, steel-toed shoes, safety glasses) as required by local procedures and the activity being performed.

Understand safe operation of the equipment within the area.

Asset Delivery

Obtain technical expertise of equipment and processes in area of responsibility.

Have a basic understanding of Infrastructure / Telecom.

General understanding of Data Flow, S95, MES (Manufacturing Execution System), SAP, and its integration with our controls systems.

Knowledgeable in multiple technologies such as Vision, PLC, VFDs, etc.

Knowledgeable in Data Integrity requirements and expectations, ensuring appropriate integration into assets within scope

Comprehensive knowledge of the code and process for assets assigned

Develop a deep understanding of Global and local requirements and expectations for Asset delivery

Understand equipment flow chart / process flow document, critical process parameters, and Control Strategy for responsible process area.

Understand design and user requirements of equipment and fundamental understanding of the operational area’s processes where the asset will reside

Understand customer needs and issues associated with new and existing process control systems.

Actively participate in project meetings, connect with delivery organizations and OEM and engage in the overall C&Q process throughout project, preparing asset for PV

Work with the project team to ensure that design, code development, and testing approaches are in line with agreed standards.

Leverage control system and electrical data to support troubleshooting, provide solutions and implement actions.

Perform activities in accordance with cGMPs and applicable procedures.

Proactively evaluate automation code to identify and correct code opportunities.

Ramp Up Phase:

Monitor, analyze, and trend data to define action plans for data integrity, process efficiency, and commercialization continuous improvements.

Monitor and enforce compliance of AQMS (Asset Qualification Monitoring Strategy), automation change strategy, and ensure compliance with all requirements, policies, and regulations.

Lead or manage small projects or initiatives related to automation technologies.

Continuously monitor and perform assessments in the assigned area of support to proactively identify opportunities and implement corrections to deliver results, drive productivity, and to be more agile and competitive

Support equipment related deviation investigations, understand potential equipment failure modes, and implement appropriate countermeasure for equipment related deviations.

Initiate change controls to optimize the systems or processes, including business case, technical recommendations, and resources / cost estimates.

Implement and/or support implementation of the change controls (complete all information, follow up approval signatures, close the document).

Participate at a Process Team member as technical SME and train individuals as appropriate to assume process automation engineering responsibilities

Fundamental Deliverables

Communicate effectively with others, especially project/process team members, customers, engineering techs, and crafts personnel.

Educate, coach, and collaborate with process team members including Operations, Maintenance, and Engineering front line staff.

Be prepared for and participate in project team meetings

Identify roadblocks and communicate to the appropriate level on time.

Use project management practices for meeting project commitments and communicate the status of initiatives to project team.

Prioritize time and task execution based on impact to business needs.

Escalate technical, safety, and quality issues as recommended by process area.

Basic Requirements

Bachelor's Degree in Engineering

Experience supporting GMP production

Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1."

Additional Preferences

Previous experience in the Pharmaceutical Industry

Previous experience in the delivery of GMP production assets

Computer System Validation experience is desirable.

Strong interpersonal and communications skills to be able to work effectively in a team-based environment

Ability to work safely to ensure the safety of self and others.

Have a basic understanding of Infrastructure / Telecom.

Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE (Health Safety and Environment) Corporate and Site Goals.

Other Information:

8-hour days, after-hour support.

Extended travel / stays may be required to support / learn from other site start- ups for similar equipment

Travel to US and OUS (4-12 weeks/yr) will be required for OEM interactions, FAT testing, and other project requirements

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

$66,000 - $171,600

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
Not listed
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 1527 comparable Manufacturing & CMC roles across 125 biopharma companies.

1527Comparable roles tracked
1434Currently active
125Companies hiring similar roles
44Countries represented

Salary context

455 of 1527 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject $66,000/yr – $171,600/yr
Lowest disclosed · Senior Scientist II – CMC Developmental Sciences · AbbVie $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $540,400 (median $140,000)

Where these roles are based

Top locations among the 1527 comparable roles

United States781
India104
Germany74
Singapore67
France64
Ireland54

+ 38 more countries

Seniority mix

705 of 1527 peers have a known seniority level

Senior251
Manager165
Principal79
Associate68
Director64
Associate Director44
Senior Director21
Intern/Fellow/Postdoc8
Executive/VP5

Therapeutic area mix

7 of 1527 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease6
Oncology1

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.

40%similar
Alexion New Haven, Connecticut, United States of America
Same function Same country
40%similar
AstraZeneca Cambridge, Massachusetts, United States of America Director
Same function Same country
40%similar
Alexion New Haven, Connecticut, United States of America
Same function Same country
40%similar
40%similar
Lilly Boston, Massachusetts, United States of America Associate
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Senior Director
Same function 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.

40%
Scientist II, LC Development, Biologics Analytical Development
Alexion · New Haven, Connecticut, United States of America · Seniority not listed
Function Therapeutic area Seniority Country
40%
Director, Global Regulatory Affairs – Chemistry, Manufacturing and Controls (CMC), Platform Innovation – Synthetic Peptides and Oligonucleotides
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
40%
Senior/Principal Scientist, Bioprocess Purification Development
Lilly · Indianapolis, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
40%
Senior Principal Scientist - Bioanalytical Research
Lilly · Louisville, Colorado, United States of America · Principal
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.