Developed, reviewed, and revised standard operating procedures (SOPs) to ensure compliance with cGMP and cGDP regulations. Manufactured T cell products with limited supervision, ensuring adherence to quality standards and meeting project timelines. Conducted mammalian cell culture activities with a focus on optimizing cell growth and viability. Collaborated with cross-functional teams to ensure efficient workflow, troubleshoot technical issues, and achieve project objectives. Experienced in facilitating cell-based assays and environmental assays on mammalian cells, analyzing and interpreting assay data. Experienced working with processing instruments such as Sepax, CliniMACS Plus, and CliniMACS Prodigy.