Individual contributor in a primarily laboratory-based role focused on the characterization of materials and processes for synthetic drug substances, including oligonucleotides, peptides, and small molecules.
Compensation
The anticipated wage for this position is $129,000 - $211,200
Responsibilities
Perform hands-on laboratory work to support the design, development, and implementation of product control strategies for oligonucleotide, peptide, and/or small molecule programs
Demonstrate proficiency in multiple analytical technologies through daily laboratory work, with an emphasis on chromatography and mass spectrometry
Execute analytical method development, generate data to justify specifications, conduct stability studies, perform starting material testing for synthetic processes, identify and characterize impurities, and test drug product performance characteristics
Conduct hands-on laboratory research to support internal process development
Provide technical input for analytical activities executed within the external network
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters.
Compensation
The anticipated wage for this position is $67,500 - $173,800
Responsibilities
Generate process design and unit operation knowledge based on engineering principles for small molecules, and other emerging therapeutic modalities.
Ensure successful scale-up of processes through fundamental engineering principles and equipment knowledge.
Design and execute laboratory experiments, including manual and automated high- and low-throughput reactors, in support of crystallization process design and optimization.
Develop drug substance processes and manufacturing technologies, with a focus on defining the physical properties of the API required for the drug product and designing crystallization processes to fulfill physical property and chemical purity requirements.
Leverage and develop process analytical technology (PAT), continuous processing, mechanistic models, and novel formulation platforms to develop well-understood and robust crystallization processes capable of enhancing or tailoring API physical properties.
Advisor, Analytical Chemistry in a laboratory‑based role focused on analytical method development, validation, and support of regulatory submissions for pharmaceutical products.
Compensation
$129,000 - $211,200
Responsibilities
Perform hands‑on laboratory work to support design, development, and implementation of product control strategies for oligonucleotide, peptide, and/or small molecule programs
Demonstrate proficiency in multiple analytical technologies with emphasis on chromatography and mass spectrometry
Execute analytical method development, generate data to justify specifications, conduct stability studies, perform starting material testing, identify and characterize impurities, and test drug product performance characteristics
Conduct hands‑on laboratory research to support internal process development
Provide technical input for analytical activities within external network and support technology transfer to CRO/CMO organizations and Lilly manufacturing sites
Requirements
PhD in Analytical Chemistry, Biochemistry, Chemistry, Materials Science, Pharmaceutical Sciences, or closely related STEM discipline
Master’s degree in Analytical Chemistry, Biochemistry, Chemistry, Materials Science, Pharmaceutical Sciences, or closely related STEM discipline with at least 8 years of pharmaceutical or biopharmaceutical development experience
Bachelor’s degree in Analytical Chemistry, Biochemistry, Chemistry, Materials Science, Pharmaceutical Sciences, or closely related STEM discipline with at least 12 years of pharmaceutical or biopharmaceutical development experience
Nice to have: PhD candidates with >2 years of post‑PhD hands‑on laboratory experience
Nice to have: Experience across multiple analytical techniques
Advisor - Analytical ChemistryLilly · Indianapolis, US