Summary

The successful candidate will work in our state-of-the-art, good manufacturing practices (GMP) facility in a team of cellprocessing technologists, growing therapeutic T-cells for the treatment of patients with viral infections and cancer. They will be manufacturing of virus-specific T-cell and tumor-specific T-cells for patient treatment.

Occasional weekends and/or extended hoursmay be required.

Job Duties

• Manufacturing therapeutic cells and cryopreservation cells for patient treatment.
• Maintains, and improves computerized databases and electronic worksheets recording activities
• Processes data and generates reports for patient files and QA/QC program.
• Supervises the activities of junior processing staff.
• Assists with the training of new staff
• Prepares media, cytokines and the other reagent for cell culture.
• Maintains equipment for use.
• Assists in the preparation and writing of abstracts, reports, papers, and presentations on the activities of the cell processing group.
• Performs other job related duties as assigned.
• Responsible for job related training, including SOP update, GMP regulation, BCM and TCH required training.
• Writes deviation reports , incident reports and validation reports.
• Attends GMP training webinars and job-related seminars and meetings
• Liaises with other groups involved in cell therapy studies, such as physicians, translational researchers, researchco-ordinators, regulatory affairs staff, quality control and quality assurance staff.
• Maintains professional and courteous relationships with other staff members.

Minimum Qualifications

• Bachelor\'s degree in Biology or related field.
• Two years of relevant experience.

Preferred Qualifications

• Master\'s in a science-related area, with at least 2 years work experience in science field, with a particular emphasis on cell and tissue culture.
• Candidate must be able to lift up to 20 pounds