Join us to lead and scale Regulatory Operations, ensuring timely global submissions and compliance as we advance innovative NK cell-based therapies. Drive cross-functional collaboration and build a high-performing team to meet our regulatory goals.

Champion quality excellence by overseeing raw material testing in GMP environments. Collaborate with internal teams and external laboratories to ensure compliance, review analytical data, and support the qualification of biologically derived materials.

Transform quality assurance in clinical programs by leading risk-based oversight, audits, and compliance efforts. Collaborate with cross-functional teams to ensure patient safety and data integrity throughout all clinical stages.