Teams at Ratio Therapeutics

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.

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

Develop, optimize, and scale radiopharmaceutical production processes; lead radiochemistry experiments and DOE/process characterization; author CMC documentation; ensure data integrity and radiation safety; automate and qualify synthesis/dispensing systems; mentor junior scientists and collaborate cross-functionally to advance programs through CMC and regulatory milestones.