Quality Assurance and Compliance Intern at Nurix Therapeutics

Department: Quality Assurance / Regulatory Compliance GxP Compliance and Document Management Intern Location: Onsite in Brisbane, CA (5 days a week) About the Role This summer paid internship supports our Quality Assurance team. The intern will complete four compliance workstreams -- auditing job descriptions, reviewing resumes on file, verifying electronic signature certifications, and updating legacy document references -- all critical to maintaining regulatory readiness. Responsibilities Maintain the complete GxP-designated user list from the Training Assignment System Audit job description completeness by cross-referencing each GxP user against existing records and tracking gaps to resolution Collaborate with users and managers to draft or finalize Job Descriptions meeting GxP standards, then upload approved documents to the Training Assignment System Verify that all GxP users have a current resume on file; conduct outreach for missing documents and upload completed records Confirm every GxP user has submitted a completed Electronic Signature Certification Form per 21 CFR Part11; follow up on incomplete submissions Audit and update legacy document references within the eDMS to reflect current versions and naming conventions Maintain clear tracking logs and follow‑up documentation throughout all workstreams Currently enrolled in or recently completed a degree in Life Sciences, Biology, Chemistry, Pharmaceutical Sciences, Healthcare Administration, or a related field Basic familiarity with GxP regulations (coursework, prior internship, or self‑study acceptable) Strong attention to detail and ability to manage multiple tasks and deadlines Proficiency with standard office software (email, spreadsheets, word processing) Clear written communication skills for professional outreach and documentation Ability to handle sensitive employee information with discretion Skills We Are Looking For Regulatory awareness: familiarity with GxP and 21CFRPart11 basics Systematic auditing and record‑keeping across large datasets Professional written communication and follow‑through Data organization using spreadsheets or tracking tools Discretion when handling employee personnel records Proactive follow‑up and independent task closure Nice to Have Prior QA or compliance internship experience Experience with a document management system 21CFRPart11 coursework or training Familiarity with electronic signature workflows or training management systems #J-18808-Ljbffr Wayne State