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Tulynode Biosciences Inc. in San Diego, CA is seeking a T cell Gene-Modification Scientist for a full‑time, on‑site role.
You will design and execute workflows to isolate, expand, and genetically modify T cells, with emphasis on lentiviral transduction and CAR‑T related constructs. You will analyze data, maintain electronic lab records, and contribute to protocol development, technology transfer, and preparation for preclinical studies and regulatory submissions, collaborating with immunology,
Company Description Tulynode Biosciences Inc. is a biotechnology company dedicated to addressing critical unmet needs in oncology by harnessing each patient’s own immune system. The company focuses on activating autologous immune cells that are specific to an individual’s tumor, aiming to deliver effective and safer cellular therapies with ex vivo manipulation. Tulynode’s gene modification strategy and “Immuno-Pod” platform is designed to expose otherwise inaccessible tumors in vivo, enhancing tumor-specific immune cell activation. This approach seamlessly integrates ex vivo and in vivo processes to create highly personalized, next-generation cancer treatments. Team members have the opportunity to contribute to innovative therapies at the intersection of immunology, gene modification, and oncology.
Role Description The T cell Gene-Modification Scientist will lead experimental design and execution to isolate, expand, and genetically modify T cells. This is a full-time, on-site role based in San Diego, CA. Daily responsibilities include designing and performing T cell modification workflows, optimizing transduction and transfection methods for packaging virus, and characterizing engineered cells using flow cytometry, molecular assays, and functional readouts (e.g., cytotoxicity, cytokine production). Emphasis would be on generating gene modifications of various types using lentiviruses.Experience with design and generation of constructs for transfer/packaging vectors for packagingis essential. The scientist will analyze and interpret data, maintain detailed electronic lab records, and present findings to cross-functional teams. The role also involves contributing to protocol development, technology transfer, and documentation to support preclinical studies, regulatory submissions, and future clinical translation, while collaborating closely with immunology, bioengineering, and operations teams.
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