Associate Director, Quality Control
Nuvalent, Inc.(2 days ago)
About this role
Nuvalent is a pioneering biotechnology company focused on developing targeted medicines for cancer treatment. The company values scientific expertise and innovation in drug discovery and oncology drug development.
Required Skills
- GMP
- ICH
- HPLC
- Stability Testing
- Method Validation
- Analytical Chemistry
- QC Management
- Regulatory Submissions
- CMC
- Statistical Analysis
Qualifications
- BS in Chemistry or related discipline, 10–15 years of industry experience, or MS/PhD with 3–5 years of experience
About Nuvalent, Inc.
nuvalent.comNuvalent is a clinical‑stage, Cambridge‑based oncology company that designs precisely targeted small‑molecule therapies using deep chemistry know‑how and structure‑based drug discovery. Its pipeline focuses on selective kinase inhibitors aimed at genetically defined cancers (ALK, ROS1, HER2 and other kinase-driven solid tumors) with the goal of overcoming resistance and improving patient outcomes. Lead programs include NVL‑520, NVL‑655 and NVL‑330, and the company highlights an approach centered on precision medicine, structure‑guided design, and translational development.
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