Biotechnician III

Role: Biotechnician III supporting cGMP manufacturing start-up and operations at BeOne’s Hopewell facility. Objectives include executing and supporting routine manufacturing activities, ensuring compliance, and assisting with facility commissioning. Responsibilities encompass hands-on cGMP production tasks such as media prep, cell culture, harvest, filtration, equipment troubleshooting, deviation management, change control, and environmental monitoring; also includes aseptic filling, labeling, packaging, and documentation. Leadership support involves acting as a temporary supervisor and assisting daily operations. Requirements: High school diploma or GED with 3+ years’ biopharma experience; familiarity with cGMP procedures, laboratory practices, and manufacturing equipment. Preferred: technical experience in biologics or cell therapy, biopharmaceutical manufacturing, or related fields; proficiency with computer systems (Word, Excel, PowerPoint). High-value specifics include work in a biologics manufacturing environment during startup, with tasks spanning bioprocessing, equipment operation, and quality documentation. Cross-functional collaboration with operations and quality teams is implied. Travel up to 5% domestically and internationally. Physical demands include prolonged standing, lifting up to 40 lbs, working with hazardous materials, and shift flexibility.