- PepGen (Boston, MA)
- We are seeking an experienced and motivated Medical Director to serve as the clinical lead for our myotonic dystrophy type 1 (DM1) program. Reporting directly to the ... with colleagues across functions (Regulatory, Commercial, Preclinical, Biometrics, and Operations ) to align on program objectives and deliverables. Stay abreast… more
- Lilly (Indianapolis, IN)
- …approaches to oligonucleotides and their conjugates as well as oligonucleotide purification, isolation, and formulation. The position presents an opportunity ... support clinical trials, product commercialization, and regulatory submissions of oligonucleotide therapeutics. Developing and working with both internal manufacturing… more
- Lilly (Lebanon, IN)
- …facility and the culture to enable a successful startup into GMP manufacturing operations ._ **Responsibilities** The Associate Director - Head of TS/MS Lab will ... to provide support to the Lebanon small molecule, peptide, and oligonucleotide manufacturing processes. Responsibilities include outfitting the TS/MS lab that is… more
- Lilly (Indianapolis, IN)
- …disease states. **Responsibilities:** The API External Manufacturing (API EM) QA Associate Director ensures that API EM operations have robust quality oversight. ... EM) provides oversight for all outsourced drug substance manufacturing operations for Lilly across multiple technical platforms. API EM...The API EM QA Associate Director is responsible for quality projects supporting API EM,… more
- Lilly (Indianapolis, IN)
- …be able to apply these learnings to a portfolio of small molecule, oligonucleotide , and synthetic peptide modalities. + Lead and/or supervise the design and ... + Experience with technical transfer of processes into manufacturing operations . Experience within the pharmaceutical sector is desired; however, other… more
- Lilly (Indianapolis, IN)
- …be able to apply these takeaways to a portfolio of small molecule, oligonucleotide , and synthetic peptide, and other emerging synthetic modalities + Possess solid ... + Experience with technical transfer of processes into manufacturing operations + Experience with authoring regulatory submissions and responding to… more
