Lilly Posted August 25, 2026

Senior Director, Novel Drug Delivery Technologies

Boston, Massachusetts, United States of America FULL_TIME
Manufacturing & CMC Senior Director
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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.

Position Overview:

The Drug Delivery group at Lilly studies physiological barriers across routes of administration to create novel, patient-centric delivery solutions, serving as a center of excellence in injection physiology, device ideation, novel drug delivery technologies across modalities and routes of administration, nanomedicine and targeted delivery, and connected devices/digital biomarkers.

This role anchors technical leadership across an expanding portfolio of novel delivery modalities and routes of administration, including inhaled/pulmonary delivery and other emerging platforms, intended to enhance delivery of biologics, small molecules, and gene therapies beyond conventional parenteral administration. We are seeking a senior technical leader to define and drive the scientific and translational strategy across this portfolio at Lilly, operating at the enterprise level: setting technical direction across programs, representing Lilly externally with academic, clinical, and regulatory stakeholders, and mentoring the next generation of engineers and scientists. The role carries accountability for translating novel delivery science from mechanistic/preclinical understanding into IND- and design-control-ready delivery platforms.

Key Responsibilities:

Define the scientific vision and multi-year technical strategy across novel drug delivery modalities (including inhaled/pulmonary delivery and other emerging platforms), aligned with the group’s portfolio bets and enterprise R&D priorities, including build-vs-buy and external innovation decisions (licensing, partnerships, sponsored research).

Serve as Lilly's internal and external technical authority across the delivery modalities in scope; lead cross-functional and cross-company teams to translate platform concepts from feasibility through design control, leveraging AI/ML-enabled simulation and data-analysis tools to accelerate technical decision-making.

Build and leverage an external network of academic collaborators, consortia, and regulatory bodies; represent Lilly's novel delivery work in publications, conferences, and regulatory or standards discussions.

Design and oversee preclinical safety/performance and efficacy study strategy with CRO and academic partners to de-risk IND-enabling and design-control decisions; champion breakthrough approaches and make data-driven, sometimes bold, decisions under scientific and technical ambiguity where no precedent exists.

Actively mentor and coach engineers and scientists, including staff outside your direct reporting line; identify and help lead scientific or process improvements that draw on diverse thinking across DDCS's broader technical portfolio.

Basic Requirements:

Earned PhD in biomedical/mechanical engineering, pharmaceutical sciences, aerosol science, or a related field.

8+ years of relevant industry/translational experience across novel, non-conventional drug delivery modalities (e.g., direct to organ delivery or a comparable parenteral platform), including demonstrated depth in the physical and biological mechanisms underlying the platform(s)

Demonstrated ability to bridge preclinical mechanistic understanding of a novel delivery platform into IND-enabling or design-control-ready translational plans

Working knowledge of design controls and quality systems in a regulated industry (systems engineering and quality partners will co-attend external engagements and can support day-to-day execution)

Effective, hands-on use of AI/ML-enabled tools (e.g., large language models, computational modeling copilots, literature-synthesis or data-analysis assistants) to accelerate scientific research, technical writing, and translational planning.

Proven ability to lead, mentor, and develop technical talent, including staff outside a direct reporting line

A publication and/or patent record demonstrating recognized technical contribution in the field; and excellent scientific communication skills across technical/non-technical and internal/external audiences.

Additional Preferences:

Experience building and sustaining external scientific relationships (academic labs, consortia, key opinion leaders); comfort representing an organization's technical position externally.

Breadth of knowledge across multiple local delivery modalities (e.g., pulmonary/inhaled, ocular, transdermal, or other emerging platforms).

Other Information:

Position Location: Boston, MA

Travel Percentage (%): 10-15

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

$166,500 - $264,000

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
Senior Director
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Boston, Massachusetts, 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 124 comparable Senior Director Manufacturing & CMC roles across 36 biopharma companies.

124Comparable roles tracked
106Currently active
36Companies hiring similar roles
15Countries represented

Salary context

68 of 124 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 $166,500/yr – $264,000/yr
Lowest disclosed · Director - Engineering Design Lead · Lilly $130,500/yr – $191,400/yr
Highest disclosed · Executive Director, CMC Regulatory Science · ModernaTX, Inc. $224,900/yr – $404,600/yr
Peer group range $160,950 – $314,750 (median $218,771)

Where these roles are based

Top locations among the 124 comparable roles

United States87
India9
Netherlands6
Ireland6
Germany3
China3

+ 9 more countries

Seniority mix

124 of 124 peers have a known seniority level

Director86
Senior Director32
Executive/VP6

Therapeutic area mix

1 of 124 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology1

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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.

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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.