Senior Quality Documentation Specialist
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Job Description & How to Apply Below
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 are looking to fill the Senior Quality Documentation Specialist position at Arrowhead Pharmaceuticals in Madison, WI, United States.
We appreciate your interest in this position.
Join Arrowhead Pharmaceuticals and contribute to our ongoing work.
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This posting is for the Senior Quality Documentation Specialist role at Arrowhead Pharmaceuticals, based in Madison, WI, United States.
Position Requirements
10+ Years work experience(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).