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Associate Director, Lipid Process Chemistry at Editas Medicine - ApplyBlast

Associate Director, Lipid Process Chemistry

Editas Medicine

21 days ago

3.4 on Glassdoor

Cambridge, Massachusetts, United States

Onsite

Full Time

Director

0 applicants

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About this role

The Associate Director of Lipid Process Chemistry leads the development, scale-up, and technical oversight of GMP manufacturing for novel lipid components in the lipid nanoparticle therapeutic pipeline. This role involves managing external CDMO partners, ensuring regulatory compliance, and driving the transition from bench-scale research to validated clinical manufacturing processes. The position requires deep expertise in organic synthesis, purification, and analytics within the advanced therapeutics industry.

Responsibilities

Lead development and scale-up of GMP manufacturing for novel lipid components
Provide technical oversight and manage external CDMO partners for lipid production
Author and review lipid excipients for regulatory submissions including INDs and IMPDs

Skills

Qualifications

Ph.D. in Organic ChemistryBS in Organic ChemistryMS in Organic Chemistry

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.