Operations Associate

Role: Manufacturing Operations Associate supporting CAR-T cell therapy production in a cGMP environment. Primary responsibilities include executing manufacturing processes such as cell culturing, purification, aseptic processing, and cryopreservation, adhering to SOPs and batch records, and ensuring compliance with quality and regulatory standards. The role involves documentation, process support, equipment operation, and participation in continuous improvement and audit activities. Requirements: High school diploma with 3-5 years biotech/pharmaceutical experience, or associate's/bachelor's degree with relevant experience; knowledge of GMP, sterile techniques, and manufacturing equipment; ability to interpret instructions and solve practical problems; physical ability to perform manufacturing tasks including lifting up to 25 lbs. Preferred qualifications include familiarity with process improvement tools and cell therapy manufacturing. High-value biopharma specifics: focus on autologous CAR-T product manufacturing for clinical and commercial use, in a regulated cGMP setting, supporting innovative immunotherapies for cancer. Collaboration involves cross-functional teams within manufacturing. Work setup: onsite in Raritan, NJ, with emphasis on safety, documentation, and team communication.