Join Our Crew

Responsibilities Include

• Assist to design and develop analytical methods for the characterization and release of lentiviral vectors and CAR-T / CAAR-T cells.
• Assist to Identify and implement opportunities for analytical method improvement and participate optimization of existing analytical methods to enhance sensitivity and efficiency.
• Perform method qualification studies in accordance with regulatory guidelines.
• Conduct quality control assays to evaluate lentiviral vectors, CAR-T / CAAR-T cells and stability samples generated by internal groups and external partners.
• Perform general lab and equipment maintenance duties.
• Participate in technical troubleshooting and problem investigation.
• Prepare, evaluate, and present data internally to cross functional teams.
• Prepare detailed and accurate documentation of experimental procedures, results, and conclusions.
• Stay current with advances in analytical techniques and industry trends.

Required Qualifications

• Bachelor’s or master’s degree in biology or closely related discipline, and with 2-4 years of experience.
• Proficient in aseptic technique for cell culture and cell-based assays.
• Strong experience in analytic techniques, including flow cytometry, qPCR/dPCR, and ELISA etc.
• Flexible to support various analytical activities and to learn new techniques outside of existing field of expertise.
• Experience with analytical method development or quality control programs for lentiviral vector and CAR-T product preferred.
• Ability to work independently and collaboratively in a fast-paced environment.
• Highly organized and strong written and verbal communication skills.
• Strong team orientation and passion for continuous self-development.
• Strong laboratory documentation practice with high scientific integrity.
• Familiarity with regulatory requirements and guidelines (FDA, ICH, etc.) for biopharmaceutical manufacturing.
• Experience in industry or in a startup industrial setting is preferred.

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