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    Senior Development Associate, Analytical Development - Cambridge, United States - Editas Medicine

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    Full time
    Description

    At Editas, we are united by a common goal: to deliver groundbreaking therapies to individuals facing severe illnesses with the most critical needs. This ambition propels us to strive for excellence in scientific advancement, enabling us to leverage the potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing.

    We firmly believe that our team members are the heart of our organization, and we are dedicated to fostering a culture where every person is valued and included. Our commitment involves promoting a sense of belonging, diversity, inclusivity, and equity throughout every facet of our company.

    Together, we are paving the way towards a healthier and more equitable future.

    Position Summary

    Editas is on the lookout for a Senior Development Associate to join our Analytical Development team. This individual will collaborate closely with various departments within research & development to carry out different biophysical techniques for gene editing components and drug product analysis. The ideal candidates will demonstrate proficiency in assay development, transferring assays to quality control, and effective teamwork across interdisciplinary groups.

    Key Responsibilities:

    • Execute a variety of biophysical techniques for analyzing gene-editing components, drug products, release, and stability.
    • Provide support for sample testing as required.
    • Collaborate with Research in assay development and enhancement.
    • Lead one or multiple assay development projects.
    • Train staff on assays when necessary.
    • Maintain thorough documentation in the electronic lab notebook (ELN).
    • Prepare and present data in meetings.
    • Contribute to the creation and review of test methods, technical reports, and related procedures.
    • Aid in transferring assays to Quality Control or central testing labs.

    Requirements

    Required Qualifications:

    • B.S. in chemistry, biotechnology, biomedical engineering, or related field with 2+ years of experience (5+ years for Associate Sci I).
    • M.S. in chemistry, biotechnology, biomedical engineering, or related field with 0-2 years of experience (3+ years for Associate Sci I).
    • Must have experience with HPLC/UHPLC assay development and sample preparation for mass spectrometry. Familiarity with various biophysical techniques is a plus.
    • Knowledge of protein or peptide analytical methods.

    Preferred Qualifications:

    • Excellent verbal and written communication skills.
    • Strong organizational abilities, including multitasking, problem-solving, and goal prioritization.

    Benefits

    Benefits Summary:

    At Editas, we offer a comprehensive benefits package to all employees, which includes medical, dental, vision insurance, life and disability coverage, tuition reimbursement, 401(k) matching, stock purchase plan, wellness programs, and flexible paid time off.

    If you are a dedicated professional with a collaborative mindset and a drive to advance transformative therapies, we encourage you to submit your application. Become part of our team at the forefront of genetic innovation and play a significant role in Editas Medicine's mission to redefine healthcare through cutting-edge genetic technologies.

    Fostering Belonging. Fueling Innovation. Transforming Lives.



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