Join us in providing technical leadership for biologics drug substance manufacturing. You’ll oversee operational processes, ensuring compliance and efficiency from late-stage development through commercialization, maximizing product quality.

Lead the charge in quality assurance for contract manufacturers, ensuring compliance and GMP oversight across critical drug production processes, while collaborating with technical teams to validate systems and processes for successful commercialization.

Join a team that's pioneering advancements in nephrology by providing scientific leadership and medical expertise to drive the Global Medical Affairs strategy for civorebrutinib and support vital clinical development initiatives.

Transform the future of nephrology by leading innovative medical strategies and fostering relationships in the biotechnology space. Bring your expertise to engage key opinion leaders and drive evidence generation for next-generation therapies.

Join a team that's redefining Medical Affairs training and operations. You'll drive innovative learning initiatives and support Medical Information activities, enhancing our scientific communication capabilities for improved patient outcomes.