Advisor – Technical Services

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.

At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.

This position is part of the Bioproduct Research and Development (BR&D) organization within Lilly Research Labs. The  &D Clinical Trial (CT) manufacturing facility is focused on bringing new protein therapeutics to market by producing bulk drug substance (DS) for clinical trials, along with the associated technical data and documentation to support GMP activities.

The Bioprocess Operations team within  &D is responsible for the manufacture of DS to support clinical trials within the Lilly portfolio. This includes the internal manufacture of monoclonal antibodies, bioconjugates, and adeno-associated viruses, as well as oversight of DS manufacturing at qualified collaboration partners.

This role serves as the Technical Lead for the Downstream Tech Service and Manufacturing Science (TS/MS) team within the  &D DS CT manufacturing facility. You will combine technical leadership with strategic execution—driving DS batch technology transfer and delivery, ensuring robust clinical manufacturing performance, and acting as a key technical interface across development, operations, automation, and maintenance teams. In addition, you will mentor and develop downstream team members, fostering a culture of technical excellence and continuous improvement.

• Lead and deliver downstream process technology transfer for Bulk DS into clinical manufacturing
• Input and authoring for cGMP and PRD Quality System compliant manufacturing master production records and review of executed batch records where applicable
• Ensure robust execution of DS batches with adherence to quality and regulatory standards
• Active oversight of process and equipment performance, troubleshooting, optimization and real-time data monitoring
• Serve as primary technical resource for downstream operations in the DS CT manufacturing pilot plant
• Drive alignment between process development and manufacturing execution
• Lead plant improvement projects focused on safety, efficiency, reliability, plant digitalization, and scalability of downstream operations
• Actively engage with HSE, Quality Assurance, Tech Services, Development, Operations, FUME/CQ, Automation, Engineering, Maintenance, Environmental Monitoring, and Manufacturing to resolve complex technical challenges.
• Coach and mentor team, fostering technical growth and professional development
• Promote a culture of collaboration, accountability, and operational excellence

• PhD in Chemical Engineering, Chemistry, Biochemistry, Biology, or related discipline with at least 3 years hands‑on purification experience OR
• MS in Chemical Engineering, Chemistry, Biochemistry, Biology, or related discipline with at least 5 years hands‑on purification experience OR
• BS in Chemical Engineering, Chemistry, Biochemistry, Biology, or related discipline with at least 8 years hands‑on purification experience
• Proficiency with UNICORN software for chromatography process control and data analysis
• Demonstrated ability to lead cross‑functional projects and mentor technical staff
• Excellent communication and leadership skills, with the ability to influence and drive change

• Understanding of cGMP requirements and regulatory compliance for clinical manufacturing
• Experie…