Biopharma QA Specialist II — GMP & Documentation Expert
Listed on 2026-10-06
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Pharmaceutical
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager
Arrowhead Pharmaceuticals, Inc. in Madison, WI is seeking a Quality Assurance Specialist II to support ongoing development programs for preclinical, clinical, and commercial drug candidates.
The role focuses on reviewing manufacturing batch records, analytical data, and related documents to ensure cGMP compliance and data integrity. The position requires a BS/BA in a scientific field, 3+ years of QA experience in biotech/pharma, strong communication, and organizational skills.
Step into the Biopharma QA Specialist II — GMP & Documentation Expert role at Arrowhead Pharmaceuticals in Madison, WI, United States and grow with us.
The Biopharma QA Specialist II — GMP & Documentation Expert role at Arrowhead Pharmaceuticals is now open for applications in Madison, WI, United States.
Join us at Arrowhead Pharmaceuticals as our next Biopharma QA Specialist II — GMP & Documentation Expert in Madison, WI, United States.
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