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You will be updated with latest job alerts via emailThis QA position will work with internal and external QA teams and QC labs ensuring adherence to compliance while supporting both clinical and commercial release and stability testing of a genetically edited cell therapy product. The position will provide compliance support to both clinical and commercial data review and data management. This person will support QA activities related to GMP release and stability as well as lifecycle improvement for methods related to raw material in-process and drug product samples. The GMP-facing nature of this work requires keen attention to detail and understanding of analytical compliance expectations.
This position is a hybrid position based in Boston that requires the ability to work independently while actively communicating key risks to management.
The Key Responsibilities are as follows:
$45-$55/hr
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (Vertex). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation medical benefits fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors including skills competencies experience location and/or being pursued and other job-related factors permitted by law. In addition this role will be eligible for overtime pay in accordance with federal and state requirements
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No C2C or Third-Party Vendors
Required Experience:
Unclear Seniority
Full-Time