Advisor/Sr Advisor/Director – Manufacturing Science (LNP Commercialization & Commercial Manufacturing Support)

100 Eli Lilly and Company; Indianapolis (IN); On-site; USD 131,000 - 211,000; Full time

Job summary

Eli Lilly and Company is seeking a scientific leader for the Parenteral Product Network TS/MS team to drive commercialization of lipid nanoparticle (LNP) drug products and provide technical support for commercial LNP manufacturing. You will be a Global Product Steward and LNP process expert, ensuring successful launches and reliable supply across sites.

You will collaborate with Product Development, Manufacturing Operations, Quality, and Supply Chain to manage technology transfer, process

Qualifications

• Degree in Biochemistry, Chemistry, Chemical Engineering, Biology, or Pharmaceutical Science with PhD/Master/Bachelor plus years of practical experience in parenteral, oligonucleotide, or nucleic acid drug development/manufacturing.
• Hands‑on experience with oligonucleotide development or manufacturing.
• Working knowledge of lipid nanoparticle formulation and manufacturing processes.
• Experience supporting GMP commercial manufacturing, including technology transfer, process validation, and deviation investigation/resolution.

Responsibilities

• Serve as Global Product Steward for LNP‑based drug products, owning end‑to‑end technical accountability for process performance, product quality, and supply across sites.
• Maintain product technical knowledge base and lifecycle strategy including risk registers and material knowledge.
• Collaborate on tech transfer, scale‑up, validation, and comparability to support commercial launch readiness.
• Provide technical support for commercial LNP manufacturing and batch execution.
• Escalate risks with assessments and mitigation plans to management.
• Own commercial control strategy for critical parameters and attributes; maintain understanding via PV, stability, and trending.
• Partner with Product Development to ensure manufacturability and provide feedback for design and site selection.
• Prepare, review, and respond to regulatory submissions and inspections readiness.
• Lead process improvement and lifecycle management projects including new technologies and raw material qualification.

Skills

LNP formulation expertise

GMP manufacturing experience

Analytical characterization of nanomr

Education

PhD in Biochemistry/Chemistry/Pharmaceutical Science with 5 years experience in parenteral or nucleic acid drug development

Master with 10 years experience in parenteral or nucleic acid drug development

Bachelor with 15 years experience in parenteral or nucleic acid drug development

Job description

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, self‑less 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.

Company Overview 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.

Position Brand Description

How would you like a career where you get to apply your best technical and analytical skills to bring a new class of genetic medicine to patients? We are seeking a scientific leader on our Parenteral Product Network Technical Services/Manufacturing Science (TS/MS) team to drive the commercialization of lipid nanoparticle (LNP) drug products and to provide technical support for commercial LNP manufacturing. In this role, you are critical to the success of Lilly’s genetic medicine portfolio. As a Global Product Steward and LNP process expert, you will hold technical ownership of LNP‑based drug products from late‑stage development through the commercial lifecycle, serving as the technical link between Product Development and our commercial manufacturing sites. You will ensure these products are successfully launched, reliably supplied, and technically well controlled across internal and external sites.

Responsibilities

As an individual contributor, you will work side by side with colleagues in Product Development, Manufacturing Operations, Quality, and Supply Chain, as well as with external manufacturing organizations. You will be a visible technical presence on and off the manufacturing floor, mentor junior technical associates, and elevate significant technical, quality, and supply risks to management with clear assessments and recommended actions.

• Serve as Global Product Steward for LNP‑based drug products, holding end‑to‑end technical accountability for process performance, product quality, and supply across all manufacturing sites, and serving as the primary technical interface between Product Development and commercial manufacturing sites.
• Maintain the product technical knowledge base and lifecycle strategy, including process history, critical material and supplier knowledge (lipids, nucleic acid payload), a product technical risk register, and a roadmap for robustness, capacity, and site‑network improvements.
• Collaborate with product development and manufacturing site for technology transfer, scale‑up, process performance qualification/validation, and comparability activities to support commercial launch readiness at internal and external sites.
• Provide technical support for commercial LNP manufacturing (e.g., microfluidic or impingement mixing, buffer exchange, tangential flow filtration/concentration, sterile filtration, fill/finish, and frozen storage), including real‑time support of batch execution and process monitoring.
• Escalate significant technical, quality, compliance, and supply risks to TS/MS management in a timely manner, providing risk assessments, impact to patients and supply, and recommended mitigation plans.
• Own the commercial control strategy for LNP critical process parameters and critical quality attributes (e.g., particle size and distribution, encapsulation efficiency, lipid and payload content, and post‑formation hold effects), and maintain process understanding through continued process verification, stability and batch trending, and global product assessment.
• Partner with Product Development to ensure manufacturability of new LNP products and platforms, and to provide commercial manufacturing feedback that informs process design, specifications, and site selection.
• Author and review technical sections of global regulatory submissions, post‑approval changes, and responses to regulatory questions, and support inspection readiness at commercial sites.
• Lead process improvement and lifecycle management projects, including introduction of new mixing, filtration, and single‑use technologies and qualification of lipid and nucleic acid raw material sources.

Basic Qualifications

• A degree in a relevant area such as Biochemistry, Chemistry, Chemical Engineering, Biology, or Pharmaceutical Science with one of the following: PhD degree with 5 years of practical experience in parenteral, oligonucleotide, or nucleic acid drug substance or drug product development and/or manufacturing, or Master degree with 10 years of practical experience in parenteral, oligonucleotide, or nucleic acid drug substance or drug product development and/or manufacturing, or Bachelor degree with 15 years of practical experience in parenteral, oligonucleotide, or nucleic acid drug substance or drug product development and/or manufacturing.
• Hands‑on experience with oligonucleotide development or manufacturing (e.g., synthesis, purification, formulation, characterization, or process development).
• Working knowledge of lipid nanoparticle formulation and manufacturing processes.
• Experience supporting GMP commercial manufacturing, including technology transfer, process validation, and/or deviation investigation and resolution.

Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H‑1B or TN status) for this employment position.

Additional Skills/Preferences

We want you to bring your oligonucleotide and nanoparticle expertise, commercial manufacturing experience, and technical influence to help launch and supply genetic medicines.

Preferred experience includes:

• Direct LNP process experience, such as microfluidic mixing, scale‑up of mixing processes, and TFF‑based downstream operations in a commercial or late‑stage clinical setting.
• Background in oligonucleotide (e.g., siRNA, antisense, mRNA, or gene‑editing payload) process, formulation, or analytical development.
• Analytical characterization of LNPs and nucleic acids (e.g., dynamic light scattering, HPLC/CE methods, encapsulation assays, and particle analysis).
• Experience with lipid excipient and critical raw material qualification, and the interaction of materials with process equipment and single‑use systems.
• Product stewardship experience, such as serving as technical owner or product lead for a commercial or late‑stage product, authoring annual product reviews or technical risk assessments, and managing multi‑site process harmonization.
• Demonstrated leadership, influence, and problem‑solving skills, including the ability to interpret complex technical data, troubleshoot manufacturing issues, and clearly elevate risks and recommendations to management.
• Preparation, review, and response to global regulatory submissions (e.g., BLAs, NDAs, or equivalent), post‑approval changes, and support of regulatory inspections.
• Working knowledge of statistical design of experiments and analysis.
• Strong written and oral communication skills, with the ability to collaborate effectively across Development, Operations, Quality, and external manufacturing partners.

We’re also excited if you bring an insatiable desire to learn, to innovate, and to challenge yourself for the benefit of patients.

Additional Information

• 10–20% domestic and international travel to commercial manufacturing sites and partners (to be confirmed by leadership).
• Lilly is an EEO/Affirmative Action Employer and 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.
• 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.

Compensation & Benefits

The anticipated wage for this position is $130,500 - $211,200. 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

At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!