About The Position

The position is a post-doctoral scientist position in the Technical Services/Manufacturing Sciences (TS/MS) organization and is available beginning January 1, 2027. It provides technical and scientific support within a dynamic manufacturing environment. They will lead the technical development and commercialization aspects for parenteral drug products to ensure process robustness and capability across multiple scales. The successful candidate will be responsible for designing and executing experiments to advance product and process knowledge, process optimization and production technical transfer, as needed. TS/ MS scientists actively contribute to the organization, and have extensive opportunities for involvement in cross-functional teams. This position allows for development of a comprehensive understanding of the pharmaceutical industry, current Good Manufacturing Practices (cGMP), regulatory requirements, and the essential role scientists play in creating solutions for Eli Lilly and Company and the patients we serve.

Requirements

  • Ph.D. in scientific disciplines of Chemistry, Materials Chemistry, Chemical Biology or closely related field.
  • 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.

Nice To Haves

  • Functional understanding of organic chemistry as applied to stability of peptides and biomolecules and characterization methods (preferred)
  • Understanding of first principles that may impact absorption/desorption properties of various materials of construction.
  • Demonstrated record of scientific achievement
  • Demonstrated problem solving abilities
  • Ability to work well independently, as well as in teams
  • Strong written and oral communication skills

Responsibilities

  • Ensuring reliability of our manufacturing processes and systems
  • Continuously searching for, developing and implementing improvements
  • Driving technical projects in a rigorous manner for robust implementation
  • Maintaining our processes in a state of compliance with US and global regulations
  • Designing and developing drug processes and delivery systems
  • Understand the chemistry and stability (including oxidation/degradation pathways) of peptides and biomolecules.
  • Develop appropriate laboratory-scale models to assess manufacturing changes.
  • Understand the scientific principles required for bioproduct manufacturing of drug substances and drug products, including the interaction of molecule/solution chemistry with process equipment, drug product containers, and/or delivery systems.
  • Design, conduct, and analyze statistically designed experiments to deepen process understanding and optimize processing conditions.
  • Understand scale-up requirements and as needed, partner with the manufacturing sites to conduct appropriate scale-up work.
  • Provide technical support to process development areas as needed.
  • Document all work in an appropriate manner.
  • Mentor lab associates enhance their technical capabilities.
  • Participate in technology transfer as needed.

Benefits

  • company bonus (depending, in part, on company and individual performance)
  • 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
  • well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Education Level

Ph.D. or professional degree

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