About the role
Job | Kyverna Therapeutics Platform & Pipeline Opportunity CAR T-Cell Therapy Pipeline Clinical Trials and Expanded Access Patients Experience Stiff Person Syndrome Myasthenia Gravis Multiple Sclerosis Lupus Nephritis Systemic Sclerosis Inside Kyverna Leadership Mission & Values Education & Events Publications Videos Investors News Careers Contact --> ← Back Senior Specialist, QA Operations Emeryville, CA Quality Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what’s possible. Title : Senior Specialist, QA Operations Location: Emeryville, CA (Hybrid) Reports To: Sr Director, Quality Assurance Operations
Responsibilities Review executed batch records and supporting documentation to ensure accuracy, completeness, and compliance with applicable
requirements. Support batch disposition and product release activities while maintaining adherence to established timelines. Consistently meet production release schedules and quality deliverables. Proactively identify, investigate, and escalate quality and compliance issues to Quality Management. Provide quality oversight and guidance regarding documentation discrepancies, deviations, and compliance-related matters. Maintain and update the vendor change notification tracking system and support the monitoring of key quality and operational performance metrics. Partner with cross-functional teams to facilitate the timely assessment, implementation, and closure of vendor change notifications. Support quality system processes, including deviations, change controls, CAPAs, and vendor change management activities. Ensure compliance with cGMP regulations, ICH guidelines, and company SOPs and quality standards. Author, review, revise, and maintain SOPs and other controlled documents to standardize and improve business processes. Contribute to continuous improvement initiatives and enhancements to the Quality Management System (QMS). Support inspection readiness activities, internal and external audits, and perform additional