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Senior Manager, Quality Validation at CRISPR Therapeutics - ApplyBlast

Senior Manager, Quality Validation

CRISPR Therapeutics

10 months ago

3.1 on Glassdoor

Framingham, MA

Onsite

Full Time

Manager

1 applicant

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About this role

A Senior Manager, Quality Validation at CRISPR Therapeutics leads the Validation and Compliance Program for the company's GMP manufacturing site in Framingham, MA. The role sits within Site Quality Assurance and focuses on ensuring regulatory compliance and quality standards for facilities, utilities, and equipment.

Skills

Qualifications

Bachelor of Science

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.