Advisor, Drug Product Process Development

Position Summary

The successful candidate will design, execute, and oversee experiments for the technical development and scale-up of lipid nanoparticle (LNP) drug product processes. This role offers a unique opportunity to independently drive LNP platform science within Orna, identify knowledge gaps, and translate cutting‑edge formulation science into robust, scalable manufacturing processes.

The successful candidate will design, execute, and oversee experiments for the technical development and scale-up of lipid nanoparticle (LNP) drug product processes. This role offers a unique opportunity to independently drive LNP platform science within Orna, identify knowledge gaps, and translate cutting‑edge formulation science into robust, scalable manufacturing processes.

Channel interactions and strategic objectives will be performed in the concerted treatment domain of the pharmaceutical manufacturing technical genetics spin‑off to integrated field transfer and cross‑platform evaluation paired with project construction and leadership management coordination while supporting the extended delivery process of lipid nanoparticles and device reagents.

• PhD, MS, or BS degree in chemical engineering, biomedical engineering, pharmaceutical sciences, chemistry, biology, or a related field with the following years of industry experience:
  PhD 0‑5 years, MS 7+ years, or BS 10+ years.
• Demonstrated hands‑on experience in formulation and process development particularly in carrier‑based or complex drug product systems (e.g., lipid nanoparticles, liposomes, emulsions, microspheres, or other advanced delivery platforms).
• Working knowledge of fluid mixing dynamics, particle self‑assembly, and surface chemistry concepts, including common characterization methods (e.g., DLS, Ribogreen, Cryo‑EM).
• Track record of independently designing and executing experiments; ability to proactively identify scientific knowledge gaps and propose structured plans to address them.

• Experience with multiple filtration technologies such as TFF hollow fibers, flat sheets, and depth filtration.
• Experience working within a matrixed CMC environment, including cross‑functional collaboration with manufacturing, analytical development, and formulation development teams.
• Strong oral and written communication skills; ability to present complex technical information clearly to diverse audiences.
• Organized, collaborative, and able to effectively partner with a diverse group of scientists, engineers, and external stakeholders.
• Proven ability to work on cross‑functional teams in a fast‑paced, dynamic environment, managing multiple priorities simultaneously.
• Detail‑oriented, self‑motivated, and enthusiastic about taking on new scientific and technical challenges.

The physical demands of this job are consistent with a laboratory environment.

Travel: < 5%

This position’s work environment is a laboratory environment.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $141,000 - $206,800.

Full‑time equivalent employees are also eligible for a company bonus (depending, in part, on company and individual performance). Lilly offers a comprehensive benefit program including a 401(k) plan; pension; vacation benefits; and medical, dental, vision, and prescription drug benefits. Additional flexible benefits such as healthcare or dependent day care flexible spending accounts, life insurance, and other time‑off and wellness benefits are also available.

See  for further assistance with accommodation requests.

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.