Nurix

Associate Director, electronic Quality Management System (eQMS)

Nurix$200K — $233K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Computer Science, Life Sciences, or related field, or equivalent experience.
  • 8+ years of experience in pharmaceutical or biotechnology industry, with 6+ years in Quality Systems/Quality Assurance.
  • Experience implementing and managing electronic Quality Management Systems (eQMS).
  • Strong knowledge of quality system data management, reporting, and data integrity principles.
  • Proficiency with Microsoft Office Suite and related business applications.

Responsibilities

  • Manage processes, SOPs, and workflows for core QMS programs.
  • Lead eQMS implementation, ensuring scalability and compliance.
  • Execute and review QMS records within the eQMS.
  • Define data governance and reporting requirements for quality systems.
  • Drive continuous improvement initiatives within the quality system.
  • Update quality policies and procedures aligned with regulatory readiness.
  • Create and deliver training related to QMS processes and eQMS functionality.

Benefits

  • Comprehensive benefits package including healthcare and retirement plans.
  • Opportunities for professional development and training.
  • Collaborative and inclusive work culture.
  • Onsite role in a modern facility in Brisbane, CA.
Full Job Description
Associate Director, electronic Quality Management System (eQMS)

Job Summary:

We are seeking an Associate Director, electronic Quality Management System (eQMS) to provide quality expertise supporting the development and commercialization of Nurix's products in compliance with relevant US, EU, and ICH requirements. In this role, you will be responsible for actively managing, developing, implementing, and reporting on Quality Systems, including Deviations, Investigations, CAPAs, Change Controls, Complaints, Quality Metrics, and electronic Quality Management Systems (eQMS). You will serve as a subject matter expert (SME) and strategic partner across Technical Operations, Clinical, Regulatory Affairs, and other cross-functional teams, with overall responsibility for the execution, scalability, and continuous improvement of Nurix's Quality Management System as the organization grows and matures.

Job Responsiblities:
  • Manage and maintain processes, SOPs, and workflows for Deviations, Investigations, CAPA, Change Control, Complaints, Quality Metrics, and other core QMS programs.
  • Lead or support the implementation, configuration, validation, and optimization of the electronic Quality Management System (eQMS), ensuring phase-appropriate design and scalability.
  • Provide hands-on expertise in the day-to-day execution, review, and management of QMS records within the eQMS.
  • Partner with internal stakeholders to define data governance, system configuration, user roles, and reporting requirements for quality systems.
  • Ensure data integrity, traceability, and compliance of quality system data in accordance with regulatory expectations (e.g., ALCOA+ principles).
  • Monitor overall quality system effectiveness, identify gaps or inefficiencies, and drive continuous improvement initiatives.
  • Recommend updates to quality policies and procedures and implement process improvements aligned with organizational growth and regulatory readiness.
  • Develop, compile, analyze, and present quality metrics and KPIs for routine management review.
  • Perform trending and data analysis to identify risks, systemic issues, and opportunities for improvement.
  • Create and deliver training programs related to QMS processes, data integrity, and eQMS functionality.
  • Support inspection readiness and ensure adherence to cGMPs, regulatory mandates, and internal quality standards.
  • Build and maintain strong cross-functional relationships and foster a culture of engagement, transparency, and quality ownership.
  • Perform other duties as assigned.

Experience and Skills:
  • Bachelor's degree in Computer Science, Life Sciences, or a related field, or equivalent relevant experience.
  • Demonstrated experience implementing, administering, and improving an eQMS, including system configuration, validation support, and lifecycle management.
  • Minimum of 8 years of experience in the pharmaceutical or biotechnology industry, including 6+ years in Quality Systems / Quality Assurance.
  • Strong working knowledge of quality system data management, reporting, and data integrity principles.
  • First-hand experience managing and reviewing deviations, investigations, CAPAs, and change controls in a regulated environment.
  • Experience using validated computerized systems to manage regulated quality records.
  • Proven ability to develop and implement enhancements to electronic Quality Systems to improve usability, compliance, and reporting.
  • Strong proficiency with Microsoft Office Suite and related business applications.
  • Ability to manage multiple priorities in a fast-paced, evolving environment with strong attention to detail.
  • Highly organized, self-motivated, and capable of working independently while effectively collaborating cross-functionally.
  • Excellent written and verbal communication skills, with the ability to influence and interact effectively at all levels of the organization.

Fit with Nurix Culture and Values
  • Strong team orientation; highly collaborative
  • Solutions and results-oriented focus
  • Hands-on approach; resourceful and open to diverse points of view

Salary Range: $200,700 - $233,500

Location: Brisbane, CA - Onsite

About Nurix

Nurix Therapeutics is a biotechnology company that is focused on the discovery, development, and commercialization of small molecule therapies that modulate the ubiquitin proteasome system (UPS) for the treatment of cancer and other diseases. The company's proprietary drug discovery platform is based on the use of DNA-encoded libraries (DELs) to identify small molecules that selectively bind to E3 ligases, which are key enzymes in the UPS. Nurix's lead drug candidate, NX-2127, is a first-in-class small molecule inhibitor of the CBL-B E3 ligase that is being developed for the treatment of solid tumors and hematological malignancies. The company was founded in 2013 and is headquartered in San Francisco, California.
Learn more about Nurix
Size
135 employees
Market Cap
$486 million
Industry
Net Income
-$43.2 million
Founded
2009
Revenue
$17.8 million
NASDAQ

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