Join our team in leading Quality Control initiatives for drug development, ensuring compliance with GMP and regulatory standards. Collaborate with cross-functional teams to drive clinical advancements in rare disease therapies and make a difference.

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 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.

Lead the commercialization of critical drug products by managing external CDMOs and cross-functional teams, ensuring quality and compliance from scale-up through validation and manufacturing phases for rare disease therapies.