Reports to the Manufacturing Manager and the Manufacturing Supervisor, and is responsible for performing cell therapy manufacturing activities in a GMP environment.
Works cooperatively with other Cell Therapy Technologists as well as with the Quality Control staff to successfully perform overall job duties.
Produce preclinical and clinical lots of material in accordance with manufacturing batch records and approved standard operating procedures while adhering to all applicable regulations and standards (i.e. GMP, GTP, AABB).
Perform simple as well as complex procedures on blood products intended for administration into patients for immunotherapeutic purposes.
Recognize, monitor and evaluate technical, instrument or physical conditions and problems.
Participate in performance improvement activities.
Assist in evaluating new technologies and process developments on tech transfer from the appropriate departments.
Other duties as required.
Minimum Education and/or Experience Required
BS degree in the life sciences (MT, biology, microbiology, cell biology), or SBB.
Minimum of 1 year of experience in aseptic processing.
State or Province