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Quality Control Analyst (Multiple Openings) at CRISPR Therapeutics - ApplyBlast

Quality Control Analyst (Multiple Openings)

CRISPR Therapeutics

4 months ago

3.1 on Glassdoor

Framingham, MA

Onsite

Full Time

Senior

0 applicants

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About this role

A full-time, lab-based QC Analyst performs in-process, final product, and stability testing for novel gene therapies in a GMP environment. The role involves supporting analytical method validation, writing SOPs, and utilizing Laboratory Information Management Systems within CRISPR Therapeutics' Framingham facility.

Responsibilities

Perform in-process and final product testing for novel drug therapies
Support implementation and validation of analytical methods
Write and revise SOPs, test methods, and compliance reports
Conduct environmental monitoring and microbiological testing
Utilize Laboratory Information Management Systems for data recording

Skills

Qualifications

Bachelor's degree in a relevant scientific area

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.