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.
How you will Achieve More with Intellia:
Intellia is looking for a Scientist focused on cell biology and assay development to support the advancement of genome editing products into the clinic. Within this role, you will be responsible for the implementation and execution of in vitro pharmacology data packages and generation of in vitro genotoxicity samples enabling in vivo and cell therapy program progression into clinical trials. You will be responsible for the documentation enabling regulatory filings including data documentation and quality control. In this role you will:
Develop appropriate cell-based models and molecular assays to measure on-target editing, target mRNA and/or protein expression level.
Work with research teams to transition relevant assays and methods from research into development through optimization to apply to regulatory programs implementing SOPs, standards, qualifications, etc
Establish and write SOPs as well as communicate data through presentation and written documentation.
Manage multiple workflow queues and requests.
Conduct experiments, troubleshoot, and optimize independently and in collaboration with colleagues to meet deadlines.
Accurately document project and sample information, protocols, and experimental details through the Laboratory Information Management System (LIMS) and Electronic Lab Notebook (ELN).
Write and QC technical and study reports to support regulatory filings (IND or CTA equivalent), and then synthesize the results for effective communication across various levels of expertise
Partner with Project Management and PreClinical Genomics on strategy and execution of in vitro sample preparation in support of genotoxicity assays
The Scientist, PreClinical in vitro pharmacology will have demonstrated expertise in cell biology, assay development, molecular biology, gene editing approaches, and experience in supporting gene editing therapies into the clinic.
PhD with 0-3 years experience directly related to industry or a BS/MS with >8/>6 years of equivalent relevant experience
Solid hands-on experience in cell culture techniques including primary cell culture. Primary hepatocytes experience is preferred.
Assay development, optimization, and qualification experience
Extensive knowledge of CRISPR gene editing approaches and genotoxicity assays.
Experience with NGS is preferred
Experience with liquid handling platforms (preferably Hamilton) is preferred.
Experience in writing and documentation to support regulatory filings is preferred.
Meet your future team:
The PreClinical team is a fun, energetic, and passionate group of individuals focused on pre-clinical Genomics data support for regulatory packages. You will report directly to the Director of Pre-clinical in vitro Pharmacology. Given the breadth of work on this team, the candidate will have the opportunity to explore a wide range of areas within the Automation, Engineering, Genomics, Informatics, and Screening (AEGIS) groups.
The team is currently working mostly onsite to execute workflows in a wet-lab environment. Therefore, we require a candidate to be currently local to Cambridge MA, or open to relocating. While much of the day-to-day operations require managing wet-lab work, our team is focused on building not just technical expertise but fostering an environment for the growth of young scientists interested in a career in biotech. If you join our team, you can expect to join a hardworking, collaborative but flexible environment. We look forward to fostering your skills, learning from your experiences, and building a larger team that will make a difference in patients' lives. We instill a culture of teamwork, respect, inclusion, collaboration, and communication ensuring that each team member strives to reach their professional and personal potential.
Covid-19 Vaccination Policy: All Intellia employees, regardless of work location, must be fully vaccinated for COVID-19. This requirement includes a booster dose once eligible. Requests for exemption for medical or sincerely held religious beliefs will be considered.
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.