Associate Director, electronic Quality Management System (eQMS)

Role: Associate Director, electronic Quality Management System (eQMS), overseeing the development, implementation, and continuous improvement of Nurix's Quality Systems to ensure compliance with US, EU, and ICH regulations during product development and commercialization. Responsibilities: manage core QMS processes (Deviations, Investigations, CAPAs, Change Controls, Complaints, Metrics), lead eQMS configuration and validation, ensure data integrity, monitor system effectiveness, develop KPIs, and support inspection readiness. Requirements: Bachelor's in Computer Science, Life Sciences, or related field; 8+ years in pharma/biotech, including 6+ years in Quality Systems/QA; extensive hands-on experience with regulated quality records, validated computerized systems, and quality data management; strong knowledge of data integrity principles and regulatory expectations. High-Value: biopharma industry, regulated environment, Quality Systems, GxP compliance, cGMP, eQMS implementation, cross-functional collaboration, data governance, and metrics reporting. WorkSetup: onsite Brisbane, CA.