Lilly Posted August 28, 2026

Process Engineer

Pleasant Prairie, Wisconsin, United States of America FULL_TIME
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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 a fortune 500 company in operation for 150 years creating high-quality medicines for our patients. The new facility on the Kenosha County campus will be one of Lilly’s most technically advanced manufacturing sites. The facility will include high-speed manufacturing, robotics, advanced data collection and analytics that will result in safety improvements, increased productivity, and variability reduction for Device Assembly/Packaging lines.   This is an exciting opportunity to help build a state-of-the-art facility and Quality System from the ground up.

Responsibilities:

As the  Process Engineer , you will be supporting and managing the Packaging crucial to Lilly's supply chain. This role will be part of the LKC Site Engineering organization responsible for the delivery of the lines and support of continuous operations by providing subject matter expertise in process control, improvements, project management, and technical leadership to the process team. This position will require the development of expertise in production processes, commissioning, qualification, and validation requirements and equipment specific code and/or control system technologies. Individuals who have passion to integrate, qualify, and start up complex Device Assembly/Packaging systems while serving as the technical bridge between OEM equipment, manufacturing control systems, MES, warehouse systems, and site operations are encouraged to apply.

Key Objectives/Deliverables:

Partner with Corporate Automation, Global Device Assembly/Packaging & Robotics, Automation Integrators, and Global Facilities Delivery to design, install, and qualify the new LKC Packaging lines.

Take overall responsibility for the safe design and safe operation of the equipment within the area.

Lead or participate in qualification activities (including commissioning activities of new equipment or areas).

Assist in the integration of these lines into the site data collection and SCADA layer.

Lead activities through the full project lifecycle including design review, FAT, installation, SAT, qualification, and startup support.

Assist for integration between Device Assembly/Packaging equipment and enterprise manufacturing systems including MES, warehouse management systems, scheduling systems, and site automation platforms.

Review OEM electrical, controls, and safety designs to ensure compliance with Lilly standards and applicable industry standards (e.g., machine safety, electrical safety, and control panel requirements).

Assist automation verification and qualification activities, including IV/OV testing, system integration testing, and startup troubleshooting.

Support implementation and lifecycle management of Lilly manufacturing platforms such as Global Packaging Platform (GPP), GRIP, GPM, Global Scheduler, and MES integrations.

Support manufacturing system interfaces including PLCs, HMI/SCADA systems, databases, servers, virtual environments, networks, and middleware platforms.

Partner with Quality, Operations, Engineering, IT, OEMs, and global platform teams to resolve complex automation and integration challenges during project execution and commercial operations.

Assist manufacturing system startup readiness activities including PSSR execution, safety verification, automation cutovers, and qualification support.

Communicate effectively with cross functional team members in roles such as quality, logistics, and crafts personnel.

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

Clear understanding of equipment flow chart, process flow document, critical process parameters, and equipment controls.

Establish control charts & monitor/trend operating parameters to verify and optimize equipment performance.

Lead troubleshooting efforts to resolve more difficult equipment and operational problems.

Utilize formal problem-solving techniques, such as root cause analysis and causal factor charting, to resolve equipment deviations.

Provide oversight and assist maintenance personnel and engineering techs that support the equipment.

Evaluate all activities for impact on qualified state of equipment and utilize appropriate tools/processes as necessary (change control, hold, etc.).

Responsible for system/component classification and maintenance strategy for equipment.

Implement corrections, corrective actions, and countermeasures arising from CAPA’s.

Participate in Periodic Reviews for equipment.

Act as user representative for capital projects or local projects.

Understand equipment reliability issues and performance KPIs.

Identify and drive improvement opportunities (procedural changes, upgrades, projects, etc.) associated with equipment within the area.

Plan and coordinate equipment planned downtime windows for equipment improvements and preventative maintenance.

Compare equipment performance data with other manufacturing sites within the network to determine areas of opportunity.

Establish & monitor/trend control systems as tool for verifying and optimizing equipment performance.

Lead troubleshooting efforts to resolve more difficult equipment and operational problems.

Utilize formal problem-solving techniques, including Root Cause Analysis, to resolve equipment issues.

Provide oversight to Maintenance Tech/Engineering Tech(s) that support the area.

Responsible for system/component classification and maintenance strategy for equipment.

Drive continuous improvement initiatives by identifying root causes, implementing robust automation solutions, and improving reliability, quality, and operational performance.

Mentor engineers and provide technical leadership across multiple manufacturing areas and project teams.

Owner/SME of equipment, Device Assembly/Packaging processes, and maintenance programs associated with Lilly Global Quality Standards (GQS) and Engineering Best Practices/Functional Standards (EBP/EFS).

Technically lead and delegate activities to a cross-functional technical team supporting the Device Assembly/Packaging lines on medium-large scale projects.

Proficient and capable of understanding OSHA/regulatory (CFR) requirements and ensuring compliance.

Requirements (Education, Experience, Training):

Bachelor’s degree in STEM

7+ years of experience as a process engineer in highly automated environment

Preferred attributes but not required:

Technical leadership.

Strong automation background.

Strong learning mindset with curiosity, adaptability, and technical aptitude to rapidly acquire new skills and technologies.

Proven experience delivering engineering projects in both greenfield and brownfield environments, including facility startup, commissioning, expansion, and retrofit initiatives.

Ability to lead first-time processes and navigating a cross-functional team through ambiguity.

Pharmaceutical cGMP experience and compliance OSHA and CFR knowledge.

Project management skills.

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

Strong knowledge of Studio 5000 and FactoryTalk View SE.

Understanding of automated vision systems, and robotics.

Ability to apply statistical thinking concepts to the analysis of manufacturing problems.

Experience in utilizing root cause analysis techniques for the systematic solving of problems.

Additional Information: 

Schedule - 8-hour days - Monday through Friday, rotational on-call support will be required.

Travel - Domestic and International travel may be required during startup phase (25-50%). Domestic and International travel may be required after Operation Readiness (5-10%).

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
Pleasant Prairie, Wisconsin, 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 2556 comparable Manufacturing & CMC roles across 173 biopharma companies.

2556Comparable roles tracked
2343Currently active
173Companies hiring similar roles
56Countries represented

Salary context

662 of 2556 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 · Associate Director, Digital Scientific Workflows · Merck $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · VP, CMC Development Technical Strategy · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $0 – $381,150 (median $122,400)

Where these roles are based

Top locations among the 2556 comparable roles

United States1232
India167
Germany134
France95
Ireland91
Netherlands77

+ 50 more countries

Seniority mix

1172 of 2556 peers have a known seniority level

Senior323
Manager265
Associate154
Intern/Fellow/Postdoc147
Principal88
Director79
Associate Director75
Senior Director34
Executive/VP7

Therapeutic area mix

12 of 2556 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease7
Rare Disease2
Oncology2
Dermatology & Aesthetics1

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
AstraZeneca New Haven, Connecticut, United States of America
Same function Same country
40%similar
40%similar
Lilly Indianapolis, Indiana, United States of America Senior Director
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Director
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Director
Same function Same country
40%similar
Lilly Louisville, Colorado, United States of America Principal
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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%
Development Scientist III, Analytical Development and Clinical Quality Control
AstraZeneca · New Haven, Connecticut, United States of America · Seniority not listed
Function Therapeutic area Seniority Country
40%
Director, Analytical Chemistry - Peptides
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
40%
Advisor, Data Scientist - CMC Data Products
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Function Therapeutic area Seniority Country
40%
Scientist - Molecular Biology, Cell Culture Upstream Process Development
Lilly · Indianapolis, Indiana, United States of America · Seniority not listed
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.