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Senior QA Specialist at Editas Medicine - ApplyBlast

Senior QA Specialist

Editas Medicine

3 months ago

3.4 on Glassdoor

Onsite

Full Time

Senior

0 applicants

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About this role

The Senior QA Specialist is responsible for ensuring the quality and reliability of biotechnology products through rigorous testing and analysis. This role involves developing test plans, executing test cases, and collaborating with cross‑functional teams to identify and resolve issues, supporting the company's commitment to high standards and regulatory compliance.

Responsibilities

Develop and execute quality assurance test plans
Validate laboratory processes and equipment
Analyze data to ensure product compliance
Collaborate with cross‑functional teams on regulatory requirements
Mentor junior QA staff and review documentation

Skills

About Editas Medicine

editasmedicine.com

Headquarters

Cambridge, Massachusetts, United States

Company Size

201-500 employees

Founded

2013

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Editas Medicine is a leading biotechnology company focused on developing CRISPR-based medicines to treat people with serious diseases. It pioneers genome-editing therapies, translating CRISPR research into clinical programs aimed at delivering transformative treatments. The company concentrates on building a pipeline of investigational medicines and collaborating across the biotech ecosystem to advance gene editing from the lab to the clinic. By leveraging precision genome editing, Editas Medicine seeks to expand treatment options for patients with previously intractable conditions.