Job Description

Key Responsibilities:

• Perform all tasks associated with the upstream portion of CAR-T manufacturing, including cell thaw, activation, transduction, and expansion in bioreactors or static culture systems.
• Operate and maintain single-use bioreactors, incubators, centrifuges, and other upstream equipment.
• Prepare and aliquot media, buffers, and other process-related solutions following aseptic techniques and SOPs.
• Execute cell culture operations in a cleanroom, maintaining strict adherence to GMP and aseptic processing standards.
• Accurately document all activities in batch records, logbooks, and electronic systems
• Collaborate with QA, QC, and MS&T teams to troubleshoot deviations and support process improvements.
• Participate in gowning qualification, environmental monitoring, and cleanroom maintenance.
• Assist in training of new team members and contribute to a positive, compliant, and efficient manufacturing environment.

Qualifications:

• Bachelor’s degree in Biology, Biotechnology, Biochemistry, or related field, or equivalent industry experience.
• 6 months or 1–3 years of experience in cell therapy, biologics, or pharmaceutical manufacturing in a GMP environment.
• Hands-on experience with cell culture, aseptic techniques, and bioreactor systems.
• Strong understanding of GMP regulations, cleanroom behavior, and safety practices.
• Ability to work a flexible schedule, including weekends or shift-based work as needed.

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