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:
As a Scientist of Critical Reagent Management, you will join the Analytical Development team within the Technical Operations group and embrace the opportunity to transform amazing sciences and technologies to powerful cures. As a Scientist within the analytical development department, you will employ your strong technical understanding of the use and assessment of biologic reference standards and critical reagents to oversee the qualification and stability of these materials. Responsibilities also include:
Support the qualification and stability assessment of new and existing reference materials and critical reagents for programs at various phases of development
Collaborate and coordinate with analytical testing sites, internal QC and SMEs to compile needed data and documentation as appropriate for trending of reference materials and critical reagents and to prepare documentation and issue memos/ Certificate of Testing
Participate in cross-functional teams to improve and optimize reference material qualification and stability processes
Work with analytical partners to implement best practices and efficiencies for reference material and critical reagent strategy
Technical and process troubleshooting and finding suitable resolutions
Author or revise procedures and other documentation to ensure the implementation and execution of sound reference material and critical reagent qualification and stability strategy in adherence to health authority expectations
Are you interested in working in the analytical development group? If you say yes, we encourage you to apply! Other qualifications and desired skills include:
M.S./ Ph.D. with 3 years of experience, or B.S with 6 or more years of experience in a relevant field required (Chemistry, Biology, Biotechnology or Chemical Engineering or related areas)
Knowledge and experience with regulatory requirements for GLP/GMP
Experience working with biological analytical methods and an understanding of analytical data generated from performing biological and biochemical analytical techniques such as cell-based assays, immunoassays, or chromatography is required
Familiarity with health authority expectations for biologic reference standards
Experience working with cross-functional teams in process and strategy improvement.
Experience interacting with health authorities and responding to health authority queries is a plus.
Excellent organizational, documentation, and communication skills; adaptive learning, critical thinking, and the ability to work well in a team
Meet your future team:
The Analytical Development team is a group of energetic, brilliant, fun and motivated individuals. We work on different modalities and still work as a team to achieve our goals. We are a small but growing family. This group is responsible for developing robust and innovative analytical methods to support internal and external manufacturing processes. We support Intellia’s clinical programs as well as in vivo and ex vivo emerging pipelines. While much of the day-to-day operations require wet-lab work, our team focus is not only on building everyone’s technical expertise but also on fostering an environment for career growth as scientists and engineers in the biopharmaceutical industry.
You will report to the Principal Scientist, Analytical Development. She loves to see people grow and develop and look forward to learning from your experiences and building the team together with you.
Covid-19 Vaccination Policy: Effective Monday, January 3, 2022, all Intellia employees, regardless of work location, must be fully vaccinated for COVID-19. 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.