The Sr. Administrative Assistant will provide specialized support to the CFO, manage calendars, travel, expenses, and assist with meetings and office management.

The Director, Process Development leads the development of T-cell therapies, overseeing GMP processes and mentoring teams while ensuring regulatory compliance.

Lead a technical program strategy team, ensuring the alignment of CMC strategies with development plans, overseeing budgets, and managing cross-functional collaboration in cell therapy projects.

The Manager/Senior Manager, Quality Systems oversees quality system activities, ensuring compliance with regulations, managing documentation, and fostering collaboration across teams to improve QMS execution.

Lead the Biostatistical group, overseeing clinical studies, ensuring statistical rigor, and collaborating on regulatory submissions and clinical development strategies.

Lead statistical programming efforts for regulatory submissions, ensuring compliance with CDISC standards and overseeing CRO work. Develop programming guidelines and solve data issues collaboratively.

The Director of Quality Compliance and Risk Management will lead efforts in GxP quality, risk management, and ensure compliance with regulatory requirements across biopharmaceutical operations.

The Cloud Systems Administrator will manage infrastructure, ensuring security, performance, compliance, and optimization while automating tasks and providing technical support.