Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations

Role: Manufacturing Associate in Cell Therapy at Bristol Myers Squibb, focused on blood component production via cell culture, harvest, and cryopreservation within a cGMP environment. Responsibilities include equipment setup, aseptic processing, data recording, deviation investigations, CAPA support, and contributing to process improvements. The position requires maintaining compliance with GMP and FDA regulations, supporting quality investigations, and adhering to safety protocols. Qualifications: High school diploma required; Bachelor's or associate degree preferred. Experience: 0-1 years in cGMP cell therapy or bioprocessing manufacturing. Skills: knowledge of cell culture, aseptic techniques, GMP/FDA regulations, basic math, technical writing, and proficiency in MS Office. High-value biopharma specifics include work in cell therapy manufacturing, handling human blood-derived components, and operating in a controlled, restricted cleanroom setting. The role operates in a team-based environment with supervision from shift management, with potential for cross-training as subject matter expert and trainer. Work setup involves shift work (e.g., Sunday-Tuesday with alternating Wednesdays) in a cleanroom environment, with physical requirements including standing, lifting, and working with PPE. Travel requirements are not specified. The position offers competitive pay, comprehensive benefits, and opportunities for professional growth within a leading cell therapy manufacturing operation.