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The Director of Quality Compliance and Risk Management at Kyverna Therapeutics will lead the establishment and enhancement of quality systems, ensuring regulatory compliance across GxP operations. They will develop a risk-based audit strategy, manage domestic and international audits, and foster collaboration between various departments to create a culture of sustainable compliance, ultimately advancing the company’s clinical development programs.

The Cloud Systems Administrator will design, deploy, and manage cloud infrastructure, ensure system availability and performance, implement security measures, automate tasks, manage backups, troubleshoot issues, and maintain documentation while collaborating with cross-functional teams.

The Director of Process Development at Kyverna Therapeutics will lead the development of processes for the expansion of genetically modified T-cells for clinical studies. Responsibilities include managing process development activities, supporting GMP manufacturing, and serving as a technical interface with CDMO partners. The role requires collaboration with various teams and maintaining regulatory compliance throughout the process development cycle.