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.

Join a team that's shaping clinical quality strategies to ensure compliance and enhance subject safety across various clinical development phases while leading audits, driving inspection readiness, and influencing key quality decisions.

Join a team that's pioneering innovative medical writing in clinical development. Collaborate across functions to deliver high-quality regulatory documents that meet stringent guidelines and timelines, ensuring scientific integrity and compliance.