Nurix Therapeutics
Senior Manager, External Quality-Supply Chain
Brisbane, California · Senior
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About the role
- The Senior Manager, Supply Chain Quality Assurance is responsible for ensuring the quality and compliance of materials, products, and distribution activities throughout the global supply chain.
- This position provides quality oversight of contract manufacturers, suppliers, warehouses, packaging operations, depots and logistics providers to ensure compliance with applicable GMP, GDP, GCP (where applicable) and company quality standards.
Responsibilities
- Qualify, monitor, and maintain approval status of suppliers, CMOs, laboratories depots and logistics providers.
- Maintain current knowledge of evolving regulatory expectations and industry standards
- Maintain current knowledge of evolving regulatory expectations and industry standards; translate requirements into practical operational guidance for the organization.
- Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases.
Requirements
- Bachelor's degree in chemistry, pharmaceutical sciences, life sciences, engineering or a related
- 5+ years of progressive Supply Chain or Supply Chain Quality Assurance experience in the pharmaceutical or biopharmaceutical industry with global distribution activities.
- Thorough knowledge of FDA regulations (21 CFR Parts 210/211) and ICH guidelines (Q7, Q8, Q9, Q10, Q11), and EudraLex - Volume 4 - Good Manufacturing Practice (GMP) and their practical application to CMC development.
- Proven track record managing quality events, deviations, CAPA programs, and change control in a clinical or commercial pharmaceutical setting.
- Experience supporting regulatory agency inspections (FDA, EMA, or equivalent).
- Thorough knowledge of FDA regulations (21 CFR Parts 210/211) and ICH guidelines (Q7, Q8, Q9, Q10, Q11), and EudraLex
Nice to have
- Experience in a clinical-stage biotech environment scaling quality operations through late-stage development and toward commercialization.
- Experience with electronic QMS platforms (e.g., Veeva Vault) and document management
- Expertise in both development-phase and pre-commercial-phase quality assurance standards and expectations.
- Strong team orientation
- highly collaborative
- Solutions and results-oriented focus
- Hands-on approach
- resourceful and open to diverse points of view
Compensation
- $173,000 - $199,00
This listing is sourced directly from Nurix Therapeutics's careers page and normalized into a canonical job model.