Cell Therapy Specialist I

Role: Cell Therapy Specialist I responsible for executing manufacturing tasks for commercial and clinical cell therapy products at a state-of-the-art facility, ensuring compliance with GMP, SOPs, and safety protocols. Responsibilities: operate, monitor, troubleshoot, and verify automated cell processing equipment in Grade B and C cleanrooms; support investigations, deviations, and change controls; maintain cGMP standards and safety practices; and identify opportunities for process improvement. Qualifications: Associate degree with at least 1 year (or High School diploma with 2+ years) relevant GMP or aseptic processing experience; preferred Bachelor’s degree; experience supporting investigations and deviations is advantageous. HighValue: cell therapy (CAR T), GMP manufacturing, clinical and commercial production, cleanroom environment, process troubleshooting, equipment operation, compliance with safety and regulatory standards. WorkSetup: on-site in Frederick, Maryland; includes requirements for PPE and cleanroom work; may involve working holidays and wearing respirators.