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Quality Site Head at CRISPR Therapeutics - ApplyBlast

Quality Site Head

CRISPR Therapeutics

23 days ago

3.1 on Glassdoor

Framingham, Massachusetts, United States

Onsite

Full Time

Director

0 applicants

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About this role

The Quality Site Head provides strategic direction and operational leadership for the Quality function at CRISPR Therapeutics' internal manufacturing facility in Framingham, MA. This role ensures end-to-end quality compliance, including FUSE qualification, materials management, and product disposition, while fostering a culture of innovation and continuous improvement. The position requires hosting audits, maintaining inspection readiness, and collaborating with internal partners to support compliant manufacturing operations.

Responsibilities

Lead strategic direction and operational leadership for site Quality function
Manage end-to-end Quality including qualification, batch record reviews, and product disposition
Host audits and Health Authority inspections to maintain site inspection readiness

Skills

Qualifications

BS in relevant scientific disciplineMS in relevant scientific discipline

About CRISPR Therapeutics

crisprtx.com

Headquarters

Boston, Massachusetts, United States

Company Size

201-500 employees

Founded

2013

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CRISPR Therapeutics is a gene-editing company pioneering the development of transformative medicines using CRISPR/Cas9 technology to treat serious diseases. The company has a broad pipeline spanning hemoglobinopathies, immuno-oncology, autoimmune diseases, in vivo editing, and regenerative medicine, including CASGEVY™, the first-ever approved CRISPR-based therapy for sickle cell disease and transfusion-dependent beta thalassemia. CRISPR Therapeutics operates across multiple clinical and preclinical programs in collaboration with partners such as Vertex Pharmaceuticals.