Nurix Therapeutics

HQ
San Francisco
Total Offices: 2
288 Total Employees
Year Founded: 2012

Nurix Therapeutics Benefits Overview

Compensation + Benefits

Offers 401(K)

Offers life insurance

Offers occupational accident insurance

Offers disability insurance

Offers supplemental life insurance

Offers accidental death & dismemberment insurance

Offers company equity

Offers performance bonuses

Offers employee stock purchase plan

Offers dental insurance

Offers health insurance

Offers mental health benefits

Offers Flexible Spending Account (FSA)

Offers vision insurance

Offers Health Savings Account (HSA)

Provides family medical leave

Offers generous parental leave

Company Culture

Provides commuter benefits

Offers travel concierge services

Provides free snacks and drinks

Offers legal assistance

Utilizes a flexible work schedule

Offers a remote work program

Work-Life Balance + Wellbeing

Offers company-sponsored outings

Offers gym membership

Offers an Employee Assistance Program (EAP)

Offers generous PTO

Provides paid sick days

Provides military leave

Provides paid holidays

Provides bereavement leave

Offers unpaid extended leave

Career Growth + Development

Provides customized development tracks

Job training & conferences

Provides tuition assistance

Healthtech • Biotech • Pharmaceutical
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.
8 Days AgoSaved
In-Office
Brisbane, CA, USA
Healthtech • Biotech • Pharmaceutical
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.
Healthtech • Biotech • Pharmaceutical
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.