Associate Scientist - Process Development

Eli Lilly Eli Lilly · Pharma · Boston, MA

Associate Scientist - Process Development role at Eli Lilly focused on leading the development and optimization of downstream purification processes for viral vector programs, from research through preclinical development. Requires expertise in ultracentrifugation, chromatography, and TFF, with experience in process development strategies and platform development.

What you'd actually do

  1. Lead development, optimization, and scale-up of downstream purification workflows for viral vectors.
  2. Design and implement purification strategieusingng Iodixanol and CsCl density gradient ultracentrifugation, affinity chromatography, ion-exchange chromatography (AEX/CEX), membrane chromatography, and polishing operations.
  3. Lead AKTA-based chromatography workflow development and process intensification initiatives.
  4. Develop scalable downstream platform approaches to support rapid material generation and process consistency across programs.
  5. Independently design experiments, analyze data, interpret results, and present technical conclusions to multi-functional teams and leadership.

Skills

Required

  • Master's degree in biology, biochemistry, chemical engineering, biotechnology or related field
  • 8+ years of relevant downstream process development experience in industry
  • Deep technical expertise in downstream purification technologies including ultracentrifugation, chromatography, and tangential flow filtration (TFF)
  • Demonstrated experience driving process development strategies, platform development initiatives, technology implementation, and multi-functional collaboration
  • Strong scientific leadership
  • Hands-on technical capability
  • Ability to independently lead complex purification development activities

Nice to have

  • CsCl and iodixanol ultracentrifugation
  • Affinity chromatography
  • Ion-exchange chromatography
  • TFF/UFDF operations including concentration, diafiltration, and formulation development
  • AKTA systems and Unicorn software
  • Strong understanding of process scale-up, platform development, and purification process characterization.
  • Experience analyzing purification performance and product quality attributes using relevant analytical methods.
  • Experience in AAV downstream process development and capsid enrichment workflows.
  • Experience with automated chromatography systems and process intensification strategies.
  • Experience supporting technology transfer and manufacturing readiness activities.
  • Familiarity with GMP development environments and regulatory expectations.

What the JD emphasized

  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization and visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.