Senior Scientist, AMP-Seq Team Lead
- Employer
- Intellia Therapeutics
- Location
- Cambridge, MA
- Start date
- Jul 13, 2024
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- Discipline
- Science/R&D, Biotechnology
- Required Education
- Doctorate/PHD/MD
- Position Type
- Full time
- Hotbed
- Genetown, Best Places to Work
Job Details
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 wantall ofour 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.
Senior Scientist, AMP-Seq Team Lead
We seek a Senior Scientist to lead the amplicon sequencing (AMP-Seq) team within the Genomics Innovation group. Genomics Innovation provides advanced genomics solutions, ranging from screening of editing modalities, to developing and implementing a diverse toolbox of sequencing assays for the characterization of genome editing outcomes. This dynamic role integrates team management in leading the AMP-Seq team and a labwork component in leveraging NGS expertise to explore and develop genomics applications with groups across the company.
AMP-seq is state of the art and operates on an industrial scale, processing tens of thousands of samples every month. It is central to the development of our genome editing technologies and builds the foundation of our diverse range of internal and external partner programs, advancing potentially life changing CRISPR/Cas9-based therapeutics. With a combination of genomics assay development ability, team leadership skills, and hands on NGS library prep and sequencer operation expertise, this role will generate opportunities to work together with research and early development teams, exploring a wide range of gene editing applications.
In this role, you will:
Lead a team of junior scientists responsible for running a high throughput Illumina amplicon sequencing workflow as well as smaller scale PacBio amplicon workflow
Chart the course for the future of AMP-Seq (e.g. process optimization, new automation workflows)
Ensure timely data delivery, working with automation and informatics teams to promptly address run failures, and work with collaborators to communicate updates and troubleshoot submissions
Apply NGS subject matter expertise to develop and support new projects and applications in Genomics
Explore and experimentally test new sequencing technologies, such as new short read sequencing platforms, duplex sequencing, and long read sequencing applications
Evaluate and implement new sequencing assays for characterizing gene editing outcomes, drawing on new published methods , new commercial kits, and internal assay development to answer emerging research questions
Present your or the team's work at project and larger team meetings
About You:
The successful candidate will have demonstrated deep expertise in Illumina NGS technology and molecular biology. The candidate should have biotech/pharma industry experience, some direct management experience, and exposure to liquid handling automation.
PhD in Genomics or related field with 2-5 years of directly relevant experience (industry experience strongly preferred)
Solid hands-on experience with Illumina library construction, quantification, instrument operation (NextSeq2000 preferred), troubleshooting, and expert level NGS knowledge
Experience directly managing junior scientists
Track record of developing, optimizing, and implementing NGS-based assays
Experience with running and optimizing liquid handling automation (Hamilton) is preferred
Experience with genome editing technologies (e.g. CRISPR) is preferred
Strong communication and documentation skills, coupled with exceptional time management skills and attention to detail
Meet your future team:
The team is focused on NGS applications for research and early development at Intellia. The focus is to predominantly support the development of new editing platforms, screening for new lead drug candidates, and evaluating drug candidate off-target editing profiles, in addition to supporting a wide range of other projects. The team is working onsite to execute NGS workflows in a wet-lab environment. Therefore, we require a candidate to be local to Cambridge MA, or open to relocating. Our team is focused on reliably delivering AMP-Seq data, improving the AMP-Seq process, and exploring innovative genomics solutions for emerging questions. In this role, you can expect to join a team of hardworking, supportive, and curious scientists in a collaborative environment.
#LI-KO2
Covid-19 Vaccination Policy:All Intellia employees, regardless of work location, are expected to follow all applicable federal, state, and local public health regulations and guidelines, and are strongly encouraged to follow all public health recommendations, including being vaccinated for COVID-19.
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.
Company
Many of us pursuing work in the biotechnology industry are inspired by a loved one who is living with a disease or the loss of someone in our community. Rare genetic and oncological and immunological diseases not only affect the people living with often debilitating and life-threatening symptoms, but these disorders also significantly impact their families, friends and caregivers.
Our researchers work tirelessly to harness the genome editing technology CRISPR/Cas9 for human therapeutic use. Jennifer Doudna, an Intellia co-founder, and Emmanuelle Charpentier were awarded the 2020 Nobel Prize in Chemistry for their pioneering work in CRISPR. We at Intellia are humbled to have a hand in making what we believe to be medical history. As a leader in this space, we take this responsibility to patients seriously.
We are employing a modular genome editing platform to create diverse in vivo and ex vivo pipelines, spanning a range of therapeutic indications. Guided by this full-spectrum approach, we are committed to making CRISPR/Cas9-based medicines a reality for patients suffering from genetic diseases and to creating novel engineered cell therapies for various cancers and autoimmune diseases.
Change life stories with genome editing therapies!
Stock Symbol: NTLA
- Website
- http://intelliatx.com/
- Phone
- (857) 285-6200
- Location
-
40 Erie Street
Cambridge
Massachusetts
02139
US
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