Teams at Ratio Therapeutics

Ratio Therapeutics invites interested candidates to upload their resumes and cover letters for potential roles in advancing cancer therapy technologies.

Lead and execute technology transfer and validation for radiopharmaceutical GMP manufacturing, including process validation, lifecycle management, documentation, training, regulatory inspection support, and cross-functional coordination during facility startup and ongoing operations.

Develop and optimize radiopharmaceutical GMP manufacturing processes and lead tech transfer to internal and external CDMO sites. Design process qualification/validation, author GMP documentation and regulatory sections, support investigations and corrective actions, train manufacturing personnel, ensure GMP/GLP compliance and inspection readiness. Occasional travel (~10%) for transfer and troubleshooting.