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© All Rights Reserved. ApplyBlast.com
Artiva Biotherapeutics
This role supports Quality Assurance Operations at a clinical-stage biotechnology company by managing document control, records management, training programs, and controlled labeling within an electronic Quality Management System. The position ensures all quality documentation, including logbooks and forms, remains accurate, current, and compliant with FDA, ISO, and GMP regulations to support the development of cell therapies.
Headquarters
San Diego, California, United States
Company Size
51-200 employees
Founded
2019
Artiva Biotherapeutics is a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies for autoimmune diseases. Their lead product candidate, AlloNK®, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs) across multiple clinical trials, including basket trials in rheumatoid arthritis and Sjögren's disease. The company leverages highly scaled, off-the-shelf, allogeneic NK cell manufacturing to make cell therapies broadly accessible to patients.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Artiva Biotherapeutics.
Artiva Biotherapeutics didn’t post a salary, so this is our estimate from similar listings.
31% below the average for this role
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