Senior Principal Chemist

4 weeks ago

Marquand, Missouri, United States Eli Lilly Full time

At Eli Lilly, we're dedicated to making life better for people around the world. Our Bioproduct Research and Development (BR&D) organization is a global leader in delivering new medicines to patients through the development and commercialization of insulins, peptides, oligonucleotides, monoclonal antibodies, novel therapeutic proteins, and gene therapy systems. We're seeking a highly skilled and motivated Senior Principal Chemist to join our team in Indianapolis, IN.

This role will involve enabling the design, development, and implementation of analytical methodologies for the characterization and analysis of cell and gene therapy products. You'll contribute to the establishment of robust control strategies through generation of data, development of analytical methods, design and execution of stability strategies. You'll also engage with scientists across development and manufacturing as well as through collaboration with external development partners to design and implement control strategies for projects at various stages of development.

Key responsibilities will include evaluating and/or implementing new analytical technologies/methods to advance Lilly's current analytical capabilities, spearheading new initiatives to improve existing scientific processes within the organization and across the company, identifying and exploiting new scientific concepts, and demonstrating strong written and verbal communication skills to speak to both technical and business-related implications of your work.

Requirements include a MS with 3+ years of drug development experience, BS with 8+ years of drug development experience, or PhD with 0-5 years of experience. Additional skills and preferences include experience with analytical control strategy development from pre-FHD to commercial launch, demonstrated proficiency with drug development for cell and gene therapy products, and knowledge of ddPCR and ELISA based methods for analysis of cell and gene therapy products.

This is an exciting opportunity to work in a dynamic environment with a diverse team of analytical chemists, pharmaceutical scientists, and engineers. If you're passionate about advancing the field of analytical chemistry and have a strong desire to make a meaningful impact, we encourage you to apply.

  • Enable the design, development, and implementation of analytical methodologies for the characterization and analysis of cell and gene therapy products.
  • Contribute to the establishment of robust control strategies through generation of data, development of analytical methods, design and execution of stability strategies.
  • Engage with scientists across development and manufacturing as well as through collaboration with external development partners to design and implement control strategies for projects at various stages of development.
  • Evaluate and/or implement new analytical technologies/methods to advance Lilly's current analytical capabilities.
  • Spearhead new initiatives to improve existing scientific processes within the organization and across the company.
  • Identify and exploit new scientific concepts.
  • Demonstrate strong written and verbal communication skills to speak to both technical and business-related implications of your work.
Requirements:
  • MS with 3+ years of drug development experience, BS with 8+ years of drug development experience, or PhD with 0-5 years of experience.
Additional Skills/Preferences:
  • Experience with analytical control strategy development from pre-FHD to commercial launch.
  • Demonstrated proficiency with drug development for cell and gene therapy products.
  • Knowledge of ddPCR and ELISA based methods for analysis of cell and gene therapy products.

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