Lilly Posted August 17, 2026

Site Master Planning and Project Engineer

KOBE, Hyogo, Japan FULL_TIME
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About this opportunity

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Site Master Planning and Project Engineer

Company: Eli Lilly Japan K.K.

Location: Seishin Laboratories

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At Lilly, we believe in the talent of our workforce. One of the best ways to utilize and develop that talent is to use our existing workforce to fill new and/or open positions. If you are looking for a new position within Lilly, you can view and apply to open roles posted in the internal job posting system. You must meet the minimum qualifications outlined in the job description and have/obtain work authorization in the country the position is located in order to be considered. When applying internally for a position, your current supervisor will receive notification that you have applied to the position. We encourage employees to discuss the opportunity with their supervisor prior to applying.

Path/Level: 

P1-P3

Note:  Roles are posted at the lowest level of a band, however, employees should search across all levels of the band to identify all opportunities.  Employees hired on banded positions (ex: P1-P3, R-path, B1-B3, etc.) transfer at their current level, despite the level indicated on the job posting.  For example, if a P2 candidate is selected for a P1-P3 banded position, the candidate will remain a P2 in the new role.

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Job Summary

The Site Master Planning and Project Engineer will be responsible for developing and implementing strategic site master plans and executing capital projects to support Eli Lilly Japan K.K.'s manufacturing and operational growth, ensuring alignment with global standards and local regulations.

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Job Responsibilities

* Strategic Planning : Develop, maintain, and update the long-range site master plan, incorporating business growth forecasts, technological advancements, operational efficiency improvements and facility fit-and-finish.

* Project Management : Lead and manage capital projects from conception to completion, including scope definition, budget development, schedule management, resource allocation, and risk mitigation.

* Engineering Design & Execution : Oversee and contribute to the engineering design, procurement, construction, and commissioning phases of various projects, ensuring adherence to safety, quality, and environmental standards.

* Stakeholder Collaboration : Collaborate effectively with internal stakeholders (e.g., manufacturing, quality, regulatory, HSE, finance) and external partners (e.g., contractors, vendors, consultants) to ensure project success and alignment with company objectives.

* Regulatory Compliance : Ensure all project activities and site master plans comply with relevant Japanese regulations, Good Manufacturing Practices (GMP), and Eli Lilly global engineering standards.

* Cost Control & Optimization : Manage project budgets, track expenditures, and identify opportunities for cost savings and process optimization without compromising quality or schedule.

* Technical Expertise : Provide technical expertise and guidance on facility design, utility systems, process equipment, and infrastructure development.

* Continuous Improvement : Identify and implement best practices in project management, engineering, and site planning to drive continuous improvement within the organization.

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Job Qualifications

* Education : Bachelor's degree in Engineering (e.g., Chemical, Mechanical, Civil, Industrial) or a related technical field. A Master's degree is a plus.

* Experience : Minimum of 7-10 years of experience in site master planning, capital project management, and engineering roles within the pharmaceutical, biotechnology, or a highly regulated manufacturing industry.

* Technical Skills :

Proven experience in leading complex engineering projects from initiation to close-out.

Strong understanding of GMP, HSE regulations, and quality systems.

Experience with facility design, utility systems, and process equipment.

* Soft Skills :

Excellent leadership, communication, and interpersonal skills with the ability to influence and collaborate across various functions and levels.

Strong analytical and problem-solving abilities.

Demonstrated ability to manage multiple projects simultaneously and prioritize effectively in a fast-paced environment.

Fluency in Japanese (written and spoken) is essential, and strong English communication skills (written and spoken) are required for interaction with global teams.

* Attributes : Proactive, detail-oriented, results-driven, and committed to continuous learning and improvement.

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 does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

#WeAreLilly

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
KOBE, Hyogo, Japan
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 2526 comparable Manufacturing & CMC roles across 157 biopharma companies.

2526Comparable roles tracked
2230Currently active
157Companies hiring similar roles
61Countries represented

Salary context

639 of 2526 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 Not listed on this posting
Lowest disclosed · Sr Manufacturing Technician · Genz. Therap Product LP $2,400/yr – $3,200/yr
Highest disclosed · Executive Director, CMC Regulatory Science · ModernaTX, Inc. $224,900/yr – $404,600/yr
Peer group range $2,800 – $314,750 (median $122,900)

Where these roles are based

Top locations among the 2526 comparable roles

United States1158
India165
Germany152
Switzerland89
France89
Netherlands87

+ 55 more countries

Seniority mix

1056 of 2526 peers have a known seniority level

Senior320
Manager267
Associate129
Principal99
Associate Director90
Director86
Senior Director33
Intern/Fellow/Postdoc26
Executive/VP6

Therapeutic area mix

5 of 2526 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease2
Vaccines & Infectious Disease1
Oncology1
Respiratory1

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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%
【今市】プロダクションエンジニア / 設備保全エンジニア
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Function Therapeutic area Seniority Country
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Function Therapeutic area Seniority Country
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埼玉:Packaging Staff(工程責任者候補)
UCB · Saitama, Saitama, Japan · 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.