Arrowhead Pharmaceuticals
Quality Specialist III, GxP Conformity & Continuous Improvement
Verona, Wisconsin, United States · Mid
Sponsorship not specified$78k-$98kDetected 6 days ago
ExcelGMPFDA RegulatoryMedical DevicesResearchAnimal StudiesMicrosoft OfficeGxP
About the role
- The QA Specialist III role is responsible for supporting Product Complaints and Quality Events, including laboratory investigations, deviations, continuous improvement initiatives, and CAPAs within Arrowhead Pharmaceutical's eQMS (Veeva).
Responsibilities
- Support eQMS workflows related to Quality Events, Product Complaints, and Internal Audits.
- Support operations with identifying root causes and determining corrective and preventive actions.
- Manage product complaint tracking, escalation, and trending.
- Write, review, and approve procedural documents.
- Participate in and support audits and inspections.
Requirements
- 6 years of experience working in a regulated environment, with a preference for quality assurance auditing.
- Competent knowledge of and ability to use Microsoft Word, Excel, and Smartsheet.
- Bachelor's degree
- Candidates must have current, valid authorization to work in the country where this role is located.
Skills
- Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
- Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
Compensation
- Wisconsin pay range
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This listing is sourced directly from Arrowhead Pharmaceuticals's careers page and normalized into a canonical job model.