Advisor - Molecular Biology, Cell Culture Upstream Process Development

Eli Lilly and Company; Indianapolis (IN); Presencial; USD 129.000 - 189.000; Jornada completa

Descripción de la vacante

Eli Lilly and Company, headquartered in Indianapolis, IN, seeks an Advisor for upstream process development in bioproduct manufacturing. You will lead cell line development, optimize culture processes, and author regulatory sections.

The role interfaces with BR&D, Discovery, and Manufacturing teams to ensure robust, scalable processes. You will transfer processes to pilot and manufacturing sites, design experiments, troubleshoot, and contribute to regulatory submissions.

Formación

• PhD in Microbiology, Cell Biology, Molecular Biology, Biology, Chemical Engineering, or related STEM with 0–3 years pharma/biotech experience.
• Strong knowledge of cell biology, culture, and recombinant protein expression.
• Excellent experimental design, data interpretation, and independent work ability.

Responsabilidades

• Design and execute upstream development experiments for bioproduct APIs.
• Provide hands-on troubleshooting and drive innovation with new ideas.
• Collaborate with BR&D, Discovery and Manufacturing groups on process development.
• Support transfer of cell culture processes to pilot plant and manufacturing sites.
• Prepare technical reports and regulatory documents.
• Engage external partners on collaborations and outsourcing efforts.
• Contribute to department goals and enable ongoing scientific activity.
• Present at conferences and publish results as appropriate.

Conocimientos

Cell biology

Cell culture

Molecular biology

Experiment design

Data interpretation

Independent work

Team collaboration

Communication

Educación

PhD in Microbiology or related STEM

Herramientas

Automation tools

AI tools

Descripción del empleo

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.

Overview

The Advisor is responsible for upstream process development activities related to the production of bioproduct active pharmaceutical ingredients including cell line development, cell culture process definition and optimization, process robustness studies, process transfers to pilot plant and manufacturing sites and authorship of upstream process development sections of Regulatory submissions.

The position will interact closely with other scientists in BR&D as well as Discovery, Technical services for Manufacturing and Manufacturing scientists. They are expected to be an integral participant on multidisciplinary CMC project teams that support bioproduct process and product development activities.

Responsibilities

• Design, execute and interpret appropriate upstream development experiments for generation of bioproduct active pharmaceutical ingredients including protein intermediates for bioconjugation.
• Provide support including hands‑on experiments for troubleshooting technical issues and driving innovation projects with novel ideas and technologies.
• Participate in cross‑functional process development teams and effectively collaborate with other groups in BR&D, Discovery, Technical services for Manufacturing and Manufacturing.
• Support transfer of cell culture processes to pilot plant and manufacturing sites.
• Author technical reports and regulatory documents.
• Work effectively with external parties on development projects, research collaborations and outsourcing efforts.
• Support organizational initiatives as needed to achieve short‑term and long‑term departmental goals.
• Engage externally through conference attendance, presentations and publications.
• Identify, partner, and develop process innovations from the outside to complement existing capabilities and areas of focus and incorporate these across the portfolio.
• Ensure work is aligned with all relevant Development Quality, Regulatory, HSE, GLP and GMP requirements.

Basic Requirements

• PhD in Microbiology, Cell Biology, Molecular Biology, Biology, Chemical Engineering, or closely related STEM discipline plus 0 - 3 years of experience in the pharmaceutical or biotech industries.
• Knowledge of cell biology, cell culture, molecular biology with an emphasis on recombinant protein expression.
• Extensive experience with designing experiments, generating data, interpreting results, and documenting the work independently.
• Ability to work well in a team environment incorporating a variety of functional relationships and desire to be a point of accountability.
• Effective oral and written communication skills, self‑management, task planning and organization.

Additional Preferences

• Postdoctoral experience is a plus.
• General knowledge and understanding of the scaling of upstream processes, and potential issues and mitigation strategies.
• Hands‑on experience with cell line generation, fed‑batch and/or perfusion cell culture processes, bioreactor control strategies, and process parameter optimization.
• Demonstrated knowledge of engineering principles and skills.
• Experience with automation and AI tools.Demonstrated strong problem‑solving and decision‑making skills.
• Work productively in an interdisciplinary team environment.

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 $129,000 - $189,200

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.

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