Search the 5 jobs at Kyverna Therapeutics

The Manager, Quality Systems will oversee and enhance the quality management systems at Kyverna, ensuring compliance with regulatory standards and fostering a culture of quality. Responsibilities include managing processes for deviations, investigations, CAPAs, and quality metrics while collaborating with Technical Operations and developing training for QMS programs.

The Manager of Quality Systems will oversee document control, training processes, and ensure compliance with quality and regulatory requirements. Key responsibilities include managing document development, implementing training plans, maintaining quality management systems, executing daily tasks in document control, and driving continuous improvement initiatives.

The Document Management Senior Specialist ensures compliance and integrity of documentation in a drug development environment. Responsibilities include overseeing the Document Management System, ensuring document compliance with regulatory standards, supporting audits, leading process improvements, and training staff.

The Senior Director of Biostatistics will lead the Biostatistical group at Kyverna Therapeutics, overseeing clinical studies and providing strategic biostatistical guidance. Responsibilities include statistical analysis execution, study design, collaboration with CROs, and regulatory interaction, ensuring the delivery of projects with rigor and quality.

The Executive Director of Strategic Sourcing and Supply Chain at Kyverna Therapeutics will build and optimize the sourcing and supply chain functions, manage critical components for cell therapy production, negotiate contracts, and ensure efficient supply networks while collaborating with various stakeholders.