Quality Assurance Specialist II - GMP & Documentation Expert
Listed on 2026-11-05
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Arrowhead Pharmaceuticals, Inc. in Madison, WI, is seeking a Quality Assurance Specialist II to support preclinical, clinical, and commercial drug candidates. You will review manufacturing batch records, analytical data, and reports, helping ensure compliance with cGMP and related quality systems.
The role requires a BS/BA in a scientific field, 3+ years in QA within biotech/pharma, and strong communication skills. Experience with GMP, GCP, GLP, ICH, and FDA guidance is preferred.
Consider building your career as a Quality Assurance Specialist II - GMP & Documentation Expert at Arrowhead Pharmaceuticals, Inc.
We are looking to fill the Quality Assurance Specialist II - GMP & Documentation Expert position at Arrowhead Pharmaceuticals, Inc. in Madison, WI, United States.
The Quality Assurance Specialist II - GMP & Documentation Expert role at Arrowhead Pharmaceuticals, Inc. is now open for applications in Madison, WI, United States.
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