Senior Quality Documentation Specialist
Listed on 2026-10-06
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Arrowhead Pharmaceuticals is seeking an experienced QA Document Control and Training Compliance specialist in Madison, WI. You will manage controlled documents, records, and training within the eQMS and LMS systems, ensuring accuracy and regulatory compliance.
Responsibilities include creating and maintaining SOPs, supporting audits, and generating compliance reports. Candidates should have 5+ years in pharma/biotech, strong organizational skills, and excellent communication abilities.
We have an opening for a Senior Quality Documentation Specialist in Madison, WI, United States within Management & Operations.
We are looking to fill the Senior Quality Documentation Specialist position at Arrowhead Pharmaceuticals in Madison, WI, United States.
The Senior Quality Documentation Specialist role at Arrowhead Pharmaceuticals is now open for applications in Madison, WI, United States.
Join us at Arrowhead Pharmaceuticals as our next Senior Quality Documentation Specialist in Madison, WI, United States.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).