- Lilly (Indianapolis, IN)
- …and operational support for market registrations and post-approval submissions. The regulatory scientist will leverage CMC technical knowledge and ... need them all over the world. We are seeking Regulatory Scientist GRA CMC -Parenteral Commercial...Products to be a part of the Lilly post-approval regulatory group to support global submissions and… more
- Lilly (Indianapolis, IN)
- …all over the world. The Senior Advisor/Director Post approval scientist in Global Regulatory Affairs - CMC commercial solid oral products will use CMC ... around the world. Lilly is looking for post approval regulatory CMC scientists to join us in... scientist will be encouraged to demonstrate innovative regulatory strategies that support the lifecycle of… more
- Lilly (Indianapolis, IN)
- …them all over the world. The Advisor Post approval scientist in Global Regulatory Affairs - CMC Commercial Products will leverage CMC technical knowledge ... around the world. Lilly is looking for post approval regulatory CMC scientists to join us in... scientist will be expected to demonstrate innovative regulatory strategies that support the lifecycle of… more
- Lilly (Indianapolis, IN)
- …that make life better for people around the world. Lilly is looking for regulatory CMC scientists to join us in developing and bringing life-changing new ... CMC technical knowledge and regulatory science expertise to drive regulatory CMC strategies and develop submissions for clinical trials and marketing… more
- Lilly (Indianapolis, IN)
- …(2025 to 2028), roles will be fluid and dynamic as we endeavor to support the project delivery, build a new organization, develop and implement the necessary systems ... and business processes required to support GMP operations. This will require significant collaboration, creativity and resilience as the Lilly Medicine Foundry goes… more
- Lilly (Indianapolis, IN)
- … climate and emerging requirements; ability to address key CMC regulatory questions that enable clinical studies and support marketing authorization ... the rapidly evolving Lilly Genetic Medicines (LGM) portfolio. The scientist will collaborate with a growing team comprised of...an opportunity to lead CMC activities to support clinical trials, product commercialization, and regulatory … more
- Lilly (Indianapolis, IN)
- …position presents an opportunity to lead CMC activities to support clinical trials and regulatory submissions of peptide/oligonucleotide therapeutics. ... needs across the rapidly evolving portfolio of medicines. The scientist will collaborate with a growing team comprised of... Support generating data to be used in regulatory filings. Possess ability to address key CMC… more