Associate Engineer, Computer Systems Validation, Quality Engineering This position supports the validation and lifecycle management of computerized systems within a regulated quality organization, ensuring compliance with cGMP, GLP, and GCP standards. Responsibilities include reviewing validation documentation, serving as an SME in CSV, managing change controls, and supporting audits and inspections. Candidates should have a science degree, 5+ years of relevant experience, and knowledge of GMP/GLP regulations. Preferred qualifications include experience with electronic document management systems. The role offers a salary range of $80,000—$95,000 USD in Wisconsin and requires US work authorization. #J-18808-Ljbffr Arrowhead Pharmaceuticals
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