Why Join Intellia?
Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.
Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We welcome challenging thoughts and imagination to develop innovative solutions. And we know that patients are counting on us to make the promise a reality, so we must maintain high standards and get it done.
We want all of our people to go beyond what is possible. We aren’t constrained by typical end rails, and we aren’t out to just “treat” people. We’re all in this for something more. We’re driven to cure and motivated for change. Just imagine the possibilities of what we can do together.
- Contribute to the design, development, and optimization of a functionally closed-system process for the manufacture of genetically modified T cells for the treatment of cancer
- Design and execute complex small-scale and full-scale experiments involving the isolation, expansion and cryopreservation of primary T cells
- Optimize gene editing in primary T cells using the CRISPR Cas9 system
- Utilize an array of analytical techniques (FACS, ELISA, qPCR, cytotoxicity) to understand the dynamics and behavior of genetically modified T cells
- Contribute to cell-based assay development by designing experiments, screening reagents, and troubleshooting critical parameters
- Interact cross functionally in order to effectively support early-stage development of product candidates
- Write SOPs, technical reports, and maintain a highly detailed electronic lab notebook
- Present data across multiple teams
- Stay informed of recent advances in the field of cell therapy by reading scientific journals and attending conferences
- Bachelor’s degree in Biochemistry, Biology, Biological Engineering, or Immunology with 5+ years of hands-on experience or Master’s degree with 2+ years.
- Previous hands-on experience with large scale closed system cell processing equipment such as CliniMACS, Sepax, Rotea, Prodigy, and Xuri bioreactors is highly desirable. Experience with clinical scale cell therapy manufacturing equipment preferred.
- Process flow design, SOP drafting and review, and development report drafting, required.
- Demonstration of aseptic cell culture techniques, including cell banking and expansion.
- Ability to work effectively with management, process and analytical development, and supply chain to aid in sourcing reagents; and evaluating multiple vendors to inform process decisions.
- Thorough knowledge of immunology with a focus on T-cell function and differentiation is required.
- Previous experience in flow cytometry, including data analysis in FlowJo and cytometer operation preferred.
- Familiarity with gene editing techniques, including electroporation and transduction.
- Self-motivated with a passion for bringing life changing therapies to patients.
- Willingness to acquire new skills and ability to work with minimal supervision.
- Ability to communicate effectively with strong writing skills, and thrive in a team with time critical objectives.
EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.