> Markdown version of [/jobs/ext/2924147-principal-scientist-in-peptide-technical-services-manufacturing-science](https://www.wearedevelopers.com/jobs/ext/2924147-principal-scientist-in-peptide-technical-services-manufacturing-science). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Principal Scientist in Peptide Technical Services & Manufacturing Science - **Company:** The Lilly Company - **Location:** Indianapolis, IN, United States - **Experience:** Expert - **Salary:** $155,000.0 - $195,000.0 - **Contract:** Permanent contract - **Skills:** Computer-Aided Design, Data Processing - **Published:** September 15, 2026 - **Apply:** https://find.jobs/jobs-near-me/apply/ats-redirect/?id=2964963356-2 ## About the Role * Peptide process development * GMP manufacturing support * Tech transfer and scale-up * Process validation * Statistical data analysis (Do * E) * Regulatory CMC/filing support * Process troubleshooting * Cross-functional project leadership * Quality and compliance expertise * Technical documentation and reporting ## Description Lilly seeks a Senior/Principal Scientist in Peptide Technical Services & Manufacturing Science to lead development, optimization, and tech transfer of peptide drug substance and drug product processes. In this role, you will design and scale robust, compliant manufacturing processes, support GMP operations, and drive process validation and continuous improvement across global sites. You will partner closely with R&D, quality, and operations to resolve complex technical issues, author regulatory and CMC documentation, and ensure reliable commercial supply. Lilly offers a collaborative, inclusive culture focused on ethical science, patient impact, and strong professional growth., * Lead development, optimization, and scale-up of peptide manufacturing processes * Support GMP manufacturing, troubleshooting, and continuous improvement initiatives * Plan and execute process validation and tech transfer to internal and external sites * Analyze process data using statistical tools to ensure robustness and scalability * Author technical reports, protocols, and regulatory/CMC documentation * Collaborate with R&D, quality, and operations to ensure reliable product supply * Ensure compliance with GMP, ICH, and internal quality standards * Mentor junior scientists and contribute to technical strategy for peptide platforms