Lilly Posted October 10, 2026

Sr. Principal Engineer - Project Planning & Scheduling

Indianapolis, Indiana, United States of America FULL_TIME
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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.

Role Summary

The Sr. Principal Engineer, Project Planning & Scheduling serves as GFD's enterprise process owner for planning and scheduling across the global capital portfolio. The role is accountable for establishing, governing, and continuously improving standards, methodologies, systems, and performance measures that support schedule development, forecasting, and execution throughout the project lifecycle. Through technical leadership, governance, and assurance, the role ensures consistent application of planning and scheduling requirements across projects, contractors, and business partners while improving schedule quality, predictability, compliance, and project delivery outcomes.

Key Responsibilities

Serve as GFD's enterprise process owner for planning and scheduling, establishing standards, governance requirements, methodologies, and performance expectations across the capital portfolio.

Develop, maintain, and continuously improve enterprise planning and scheduling standards, procedures, work instructions, templates, and assurance frameworks.

Establish scheduling requirements for all phases of project delivery, including project development, engineering, procurement, construction, commissioning, qualification and validation (CQV), startup, operational readiness, and operational handover.

Define and govern schedule quality requirements, including schedule development, logic integrity, critical path methodology, progress measurement, forecasting, schedule risk analysis, and schedule performance management.

Lead planning and scheduling assurance activities across the portfolio to verify compliance with enterprise standards and drive corrective actions where deficiencies are identified.

Establish planning and scheduling requirements for contractors, consultants, and delivery partners and ensure consistent implementation across projects and regions.

Serve as GFD's senior technical SME for schedule recovery, acceleration planning, scenario analysis, forecasting, and schedule risk mitigation.

Govern enterprise KPIs and performance measures related to schedule quality, forecasting accuracy, schedule predictability, and project delivery performance.

Partner with project teams, contractors, and business partners to improve scheduling capability, strengthen project execution strategies, and promote adoption of best practices.

Build organizational capability through training, mentoring, communities of practice, and continuous improvement initiatives that advance planning and scheduling excellence across the portfolio.

Minimum Qualifications

Bachelor's degree in Engineering, Construction Management, Architecture, Business, Supply Chain, or a related discipline, or equivalent work experience.

Demonstrated expertise in planning and scheduling for large, complex capital projects, including development, governance, and assurance of integrated schedules, application of critical path methodology, forecasting, schedule risk analysis, and establishment of enterprise scheduling standards and best practices.

Proficiency with Primavera P6

Ability and willingness to travel up to 25%.

Position is based in Indianapolis, Indiana.

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.

Preferred Qualifications

Professional certification from AACE International, PMI, CMAA, or a similar professional organization.

Experience serving as a planning and scheduling lead, center-of-excellence lead, or process owner supporting large capital project portfolios.

Experience supporting integrated project delivery across engineering, procurement, construction, commissioning, qualification and validation (CQV), startup, operational readiness, and operational handover.

Experience supporting pharmaceutical, biotechnology, life sciences, advanced manufacturing, or other complex industrial capital programs, including contractor scheduling governance and assurance.

Proficiency with enterprise planning, scheduling, project controls, and project information management systems, including application of integrated master scheduling, schedule assurance, schedule recovery, scenario analysis, KPI management, and portfolio performance reporting.

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

$67,500 - $173,800

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
Principal
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 683 comparable Principal Manufacturing & CMC roles across 89 biopharma companies.

683Comparable roles tracked
620Currently active
89Companies hiring similar roles
34Countries represented

Salary context

264 of 683 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 $67,500/yr – $173,800/yr
Lowest disclosed · Senior Technician Calibration - Maintenance · Mylan Technologies, Inc. $37,000/yr – $80,000/yr
Peer group range $58,500 – $288,000 (median $154,950)

Where these roles are based

Top locations among the 683 comparable roles

United States451
India38
Ireland33
Netherlands23
Germany15
Switzerland14

+ 28 more countries

Seniority mix

683 of 683 peers have a known seniority level

Senior431
Principal137
Director115

Therapeutic area mix

9 of 683 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease4
Oncology3
Respiratory1
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.

60%similar
Merck Rahway, New Jersey, United States of America Principal
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Principal
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Principal
Same function Same seniority Same country
60%similar
AbbVie Pleasanton, CA Principal
Same function Same seniority Same country
60%similar
Sanofi US Services Inc. Waltham, United States Principal
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Tarrytown, United States Principal
Same function Same seniority Same country

Notify me about similar jobs

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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%
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Function Therapeutic area Seniority Country
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AbbVie · North Chicago, IL · Principal
Function Therapeutic area Seniority Country
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Regeneron Pharmaceuticals, Inc (USA) · Tarrytown, United States · Principal
Function Therapeutic area Seniority Country
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Lilly · Concord, North Carolina, 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.