The Cell Therapy Associate III is responsible for the manufacturing of cellular therapeutics for clinical applications within a cGMP environment and reporting manufacturing data. This role requires skills to perform complex manufacturing operations with direct interaction with cellular products under minimal supervision.
- Manufacture cell therapy products per manufacturing batch records and in compliance with current regulations and quality standards. The duties required include basic cell culture and specialized cell culture techniques including, but not limited to, cell selection, transduction, and purification protocols.
- Collaborate with Development to transfer new procedures into Manufacturing.
- Perform operations in a cleanroom environment, applying controls to assure aseptic processing including gowning, cleaning, and isolation procedures.
- Train junior associates on technical and facility cleaning procedures, analyze manufacturing data for trending, work with others to assist in transfer of new procedures into manufacturing.
Associate Degree with 6 years or Bachelor’s degree with minimum 4 years’ GMP experience, preferably in cell therapy manufacturing.
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or Vietnam veteran status, are strongly encouraged to apply.