Lentivirus Manufacturing Operator

Role: Lentivirus Manufacturing Operator responsible for producing lentivirus vectors for autologous CAR-T therapies within a cGMP cleanroom. Responsibilities include executing process unit operations such as cell culture (shake flasks, bioreactors), virus harvest, purification, filtration, and sterile filling, while maintaining compliance with GMP, GDP, and safety protocols. The role involves documenting batch data, supporting process development, and participating in continuous process improvements. Qualifications: High school diploma with 1-2 years’ relevant experience or an associate’s/bachelor’s degree in Chemical Engineering, Biological Sciences, Chemistry, or Biochemistry. Preferred experience in biopharmaceutical manufacturing, aseptic processing, GMP compliance, and industry-specific operations. Skills include knowledge of GMP, process execution, data management, and communication, with proficiency in Microsoft Office. Work in Raritan, NJ, with up to 10% domestic travel, day shifts, and flexibility for schedule adjustments. The position emphasizes team collaboration in a fast-paced biotech manufacturing environment, supporting cell therapy production for innovative medicine applications.