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- Develop analytical testing and characterization methods to evaluate drug substance and drug product attributes, identify technical risks, and collaborate toward risk mitigation strategies.
- Oversight and execution of analytical development, validation, and testing operations both internally and at external CDMO/CRO partners.
- Author relevant sections of regulatory filings.
- Expertise in chromatographic method development, impurity and stability characterization, and phase-appropriate control strategy.
- Record of contribution to Phase 1 INDs, and experience in vendor oversight.
Associate Director, Analytical Development and Quality Control - San Francisco - Nurix, Inc.

Description
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines. These medicines represent the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases.
The company's fully AI-integrated discovery engine enables it to tackle any protein class, and its unparalleled ligase expertise gives Nurix a formidable advantage in translating the science of targeted protein degradation into clinical advancements.
Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Job Title: Associate Director, Analytical Development and Quality Control
Nurix Therapeutics seeks an experienced Associate Director to lead IND-enabling and early phase analytical development within the Analytical Development and Quality Control group.
Key Responsibilities:
Requirements:
About Us:
Nurix Therapeutics is a clinical stage biopharmaceutical company dedicated to improving treatment options for patients with cancer and inflammatory diseases through the discovery, development, and commercialization of targeted protein degradation medicines.
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