Advisor - Purification Process Translation and Execution Lilly Medicine Foundry

Eli Lilly and Company; Lebanon (IN); On-site; USD 127,000 - 211,000; Full time

Benefits offered by this job

Annual bonus

Comprehensive benefits

401(k) plan

Job summary

Eli Lilly and Company in Indianapolis, Indiana, invites qualified scientists to join the Lilly Medicines Foundry in Lebanon. You will oversee API/DS transfer, ensure process fit, and support scalable, right-first-time manufacturing in a high-impact, fast-paced environment.

This role requires BS/MS/PhD in relevant fields and 4+ years in biologics or conjugates product/process development. You will mentor junior staff, collaborate across PRD/CMC, and contribute to continuous improvement and

Qualifications

• BS required with 15+ years, MS with 10+ years, or PhD with 4+ years in Biologics/Drug Conjugates Product/Process Development or related roles
• Strong knowledge of bioprocesses including upstream/downstream processes and aseptic processing
• Experience in data analysis, regulatory compliance and cGMP environments

Responsibilities

• Oversee transfer of API/DS processes from development to Foundry, focusing on purification and scalability
• Monitor manufacturing processes, analyze data, and author technical reports and change controls
• Support creation/review of batch records, process descriptions, and risk assessments ensuring regulatory compliance
• Collaborate across Foundry, PRD/CMC to achieve project goals
• Lead or assist investigations and CAPA to maintain product quality and timelines
• Provide scientific input during audits and mentor junior staff in lab procedures and data analysis
• Apply scientific knowledge to troubleshoot issues and implement improvements
• Collaborate with Tech Lilly and Digital Innovation to adopt transformative technologies

Skills

Bioprocess knowledge

Root cause analysis

Communication skills

Cross-functional collaboration

Regulatory knowledge

Project management

Mentoring

Continuous improvement

Education

BS/MS/PhD in Biology/Biochemistry/Biological Engineering/Chemical/Biochemical Engineering

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, 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.

Organization And Function Overview

Lilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a pioneering center that integrates advanced manufacturing and drug development. As the first facility of its kind, the Foundry is designed to accelerate innovation in manufacturing processes, expand capacity for clinical trial medicines, and speed Lilly innovative medicine to Clinics, and reduce both costs and environmental impact.

Key Responsibilities

• Process Transfer and Production Support: Oversee the successful transfer of API/DS processes from development to Foundry with a focus on purification and flexibility in supporting multiple modalities, including Biologics, ADCs, Tides, ensuring process fit to plant, scalability, and right-first-time execution.
• Data Analysis and Reporting: Monitor manufacturing processes, analyze experimental and production data, and author technical reports, protocols, and change controls.
• Documentation and Compliance: Support the creation and review of technical documents, batch records, process descriptions, and risk assessments, ensuring adherence to cGMP and regulatory standards.
• Cross-Functional Collaboration: Work closely with various functions within Foundry and across PRD/CMC to achieve project goals and ensure product quality.
• Investigations and CAPA Support: Lead or assist in process-related investigations, assess deviations, design and conduct needed lab studies, and support Corrective and Preventive Actions (CAPAs) to maintain product quality and timelines.
• Technical Expertise: Provide scientific input during audits, provide on-floor support for critical operations, and mentor or supervise junior scientists or technicians in laboratory procedures, data analysis and related PTE activities.
• Continuous Improvement: Apply scientific knowledge to troubleshoot production issues, identify areas for improvement, design and conduct lab studies, and implement new technologies or procedures.
• Site Technology Agenda & Innovation: Collaborate with PRD, Process Engineering, and leverage internal/external/academic partnerships to accelerate innovation, including scouting, assessing, developing, and implementing new technologies. Collaborate with Tech Lilly and Digital Innovation to contribute to identification and implementation of transformative technologies and methodologies to accelerate technology transfer, minimize translation errors, and drive continuous improvement.

Basic Requirements

• Education: BS, MS or PhD in Biology, Biochemistry, Biological Engineering, Chemical/Biochemical Engineering, or related disciplines
• Experience: BS with 15+ years, or MS with 10+ years, or PhD with 4+ years in Biologics/Drug Conjugates Product/Process Development, Manufacturing Technical Services, or related functional roles

Additional Skills And Preferences

• Technical Expertise: Strong knowledge of bioprocesses (upstream or downstream, including cell culture, centrifugation, filtration, chromatography, conjugation, and aseptic processing).
• Problem-Solving Skills: Proven ability to analyze data, perform root cause analysis, and resolve complex technical challenges.
• Communication Skills: Excellent written and verbal communication skills for technical report writing, presentations, and effective collaboration across teams.
• Collaboration: Demonstrated success in cross-functional, dynamic, and matrixed environments.
• Regulatory Knowledge: Solid understanding of biopharmaceutical manufacturing principles and cGMP requirements.
• Scientific Curiosity: Proactive engagement with external innovation and industry trends.
• Project Management: Experience in leading small projects, coordinating activities, and managing timelines to meet project goals.
• Supervisory Experience: preferred

Other Information

• Initial location at Lilly Technology Center, Indianapolis and/or Parkwood West
• Permanent location at the new Lilly Medicines Foundry in Lebanon, Indiana.
• Limited domestic and international travel (< 5%) may be required for this role
• Role requires ability to work in manufacturing and laboratory environments.

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
$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.

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