At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases.
Why Choose Editas?
At Editas Medicine, we’re a team of courageous problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what’s possible in medicine, come join us and become an Editor!
Decoding The Role:
As a Scientist II, Advanced Technology Group, you’ll be a vital contributor to our mission and our success. The Editing Technology and Molecular Biology Team at Editas focus on developing novel gene editing technologies for current and future therapeutic programs and is looking to add highly talented and motivated candidate to help develop precise gene correction and insertion platforms for advancing new therapies. This individual will lead the development of novel gene editing technologies and implement these technologies to treat therapeutic indications with significant unmet medical needs. In addition, they will provide molecular biology and cloning support to Editas’ in vitro and in vivo pre-clinical studies. With a strong background in molecular and cellular biology, this person will work within cross-functional teams including Discovery, Human Genetics and Genomics, Platform Technology, Translational Science in development and commercialization of gene therapy drug products.
Characterizing Your Impact:
As the Scientist II, Advanced Technology Group, you will:
- Leverage expertise in molecular biology, cell biology, human genomics to develop novel editing technologies that enable expanded editing capabilities (precision editing, targeted insertion and integration).
- Lead and develop projects and processes for the successful translation of gene editing technology into clinical development.
- Work cross-functionally to drive technology and program development.
- Generate data in a timely manner and within deadlines.
- Maintain clear and detailed electronic notebook and records, and prepare written data reports and figures, and present research results to other team members.
- Provide training and mentorship to junior scientists and associates.
- Additional duties may be assigned if necessary.
The Ideal Transcript:
To thrive in this role, you’ll need
- Ph.D. in cell biology, molecular biology, bioengineering, or a related field with a track record of productivity and qualification.
- 2+ years of industry experience in molecular biology or a related field.
- Prior experience related to gene therapy, gene editing and targeting.
- Molecular biology expertise including DNA recombineering, vector construction, RNA/DNA isolation and quantification (e.g. qPCR and ddPCR), next generation sequencing, western blotting, immunoprecipitation, ELISA, etc.
- Cell biology expertise including mammalian cell and tissue culture, transient and stable transduction (e.g. AAV, retroviral vectors) and transfection (e.g. nucleofection, lipofection), fluorescence microscopy, immunostaining, and flow cytometry.
- Hands-on experience developing in vitro and/or cell-based high throughput assays.
- Direct experience of in vivo studies with animal models is ideal.
- Strong critical thinking and problem-solving abilities for independent project design, execution and troubleshooting.
- Outstanding communication skills, both written and oral, and an ability to work in a team-oriented, multidisciplinary environment.
- Proven track record of collaborating with cross-functional teams.
Benefits Summary:
Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Stock Purchase Plan, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy.
Aspire to be an Editor? We invite you to apply and join us at the forefront of innovation and be a key contributor to realizing Editas Medicine's mission of developing transformative medicines for people living with serious diseases.
Top Skills
What We Do
What if you could repair broken genes? That is the question we ask ourselves every day at Editas Medicine. We’re a leading genome editing company focused on translating the power and promise of our proprietary genome editing systems into medicines to help transform the lives of people with genetically-defined diseases. Our goal is to discover, develop, manufacture, and commercialize transformative medicines for a range of serious diseases, including eye diseases, blood diseases, and cancer.
We are a vibrant company full of hope, possibilities, and a belief that, working together as One Editas, we can truly revolutionize the development of medicines. We are on an important journey to unlock the full potential of genome editing technology. A journey fueled by our distinct culture, expert team of Editas Medicine ‘Editors’, and the patients we aspire to help around the world. Connect with us to hear about the tremendous progress and scientific advancements we’ve already made and the next breakthrough on the horizon. If you are ingenious, passionate and resilient, come join the revolution. Repairing broken genes is only the beginning.