Teams at Nurix Therapeutics

Manage and improve Nurix’s electronic Quality Management System and core quality processes, including deviations, investigations, CAPAs, change controls, complaints, metrics, and data integrity. Lead eQMS implementation, configuration, validation, lifecycle management, reporting, and continuous improvement. Partner cross-functionally to support regulatory compliance, cGMP adherence, inspection readiness, training, and scalable quality-system operations across the growing biotechnology organization.

Leads nonclinical toxicology operations and program management for biopharmaceutical discovery programs from late lead optimization through IND filing. Responsibilities include planning GLP and non-GLP studies, managing CROs and contracts, tracking budgets and timelines, coordinating cross-functional teams, maintaining program dashboards and risk registers, supporting regulatory submissions, and driving milestone and decision-making processes across toxicology, DMPK, pharmacology, CMC, chemistry, and regulatory functions.

Leads analytical development and quality control activities for IND-enabling and early-phase clinical studies. Develops and validates methods, characterizes drug substances and products, manages stability programs, investigates deviations and out-of-specification results, and oversees analytical work at internal and external partners. Reviews technical documentation, establishes specifications and control strategies, supports regulatory filings, and ensures cGMP and SOP compliance. The role is onsite in Brisbane, California, with domestic and international travel.