Principal Process Engineer, Parenteral Drug Product Development

LI Test Company(20 days ago)

United States, Indianapolis, INOnsiteFull TimeSenior$79,500 - $148,500Bioproduct Research and Development (BR&D)

About this role

Principal Process Engineer on Lilly’s Bioproduct Research & Development team focused on development and commercialization of parenteral biologic drug products. The role supports platforms including monoclonal antibodies, therapeutic proteins and peptides, oligonucleotides, LNPs, ADCs and other delivery modalities. The position is based at Lilly Technology Center in Indianapolis and works in a laboratory environment.

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Required Skills

Process Development
Tech Transfer
Process Qualification
Regulatory Submissions
cGMP Compliance
LNP Manufacturing
ADC Development
Stability Testing
Statistical Analysis
Cross-Functional Collaboration

Qualifications

B.S. in Pharmaceutical Chemistry
M.S. in Pharmaceutical Chemistry
B.S. in Engineering
M.S. in Engineering
US Work Authorization

About LI Test Company

lilly.com

Eli Lilly and Company is a global biopharmaceutical company headquartered in Indianapolis, Indiana. It discovers, develops, manufactures and commercializes prescription medicines across therapeutic areas including diabetes, oncology, immunology, neuroscience and pain, and has a longstanding history in insulin and other major drug discoveries. Lilly invests heavily in research and clinical development and partners with biotech, academic institutions, and industry collaborators to advance biologics, small molecules, and precision medicines. The company operates global manufacturing and commercial networks and provides patient-support programs to improve access to its therapies.

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