Editas Medicine

At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing.

We believe our people are at the core of everything we do, and we’re committed to cultivating a culture where every individual feels valued and included. To do this, we strive to integrate belonging, inclusivity, diversity, and equity into every aspect of our organization.

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

Position Summary

Editas is seeking a Senior Development Associate to join our Analytical Development group. This person will work closely with teams across research & development to execute various biophysical methods for gene editing components and drug product characterization. Ideal candidates will have demonstrated experience with assay development, tech transfer of assays to QC, and the ability to work collaboratively across cross-functional teams.

Key Responsibilities:

• As the Senior Development Associate, you will be responsible for:
• Development and execution of various biophysical methods to gene-editing components and drug product characterization, release, and stability.
• Support testing of various samples as needed.
• Work collaboratively with Research to perform assay development and optimization.
• Opportunity to spearhead one or multiple assay development projects.
• Cross-train personnel on assays, as required.
• Meticulous documentation in electronic lab notebook (ELN).
• Compile and present data in various meetings.
• Assist in authoring and reviewing of test methods, technical reports, and supporting procedures.
• Assist in the technical transfer of assays to Quality Control or central testing laboratories.

Requirements

Required Qualifications:

The ideal candidate will possess:

• B.S. in chemistry, biotechnology, biomedical engineering, or related field with 2+ years of relevant experience (5+ years for Associate Sci I)
• M.S. in chemistry, biotechnology, biomedical engineering, or related field with 0-2 years of relevant experience (3+ years for Associate Sci I)
• Experience and/or familiarity with HPLC/UHPLC assay development is required. Experience and/or familiarity with sample preparation for mass spectrometry is required. Experience with various biophysical techniques such as icIEF, CE-SDS, static and dynamic light scattering, and mass spectrometry is preferred.
• Familiarity with protein or peptide analytical techniques.

Preferred Qualifications:

Additionally, candidates with the following attributes are preferred:

• Strong verbal and written communication skills.
• Strong organizational skills with the ability to multi-task, problem-solve, prioritize assignments, and adjust priorities to meet goals.

Benefits

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.

If you are a results-focused and collaborative professional with a passion for advancing transformative therapies, we invite you to apply. Join us at the forefront of genetic innovation and be a key contributor to Editas Medicine's mission of redefining healthcare through cutting-edge genetic technologies.

Fostering Belonging. Fueling Innovation. Transforming Lives.