Description
Serán BioScience is hiring an experienced Quality Assurance Associate to support regulatory compliance and quality systems for the clinical manufacturing of oral solid dosage drug products. The role includes reviewing and approving production records, analytical data, and QA documentation; supporting GMP and SOP compliance; conducting risk analyses and investigations; managing CAPA programs; and participating in audits and inspections. Candidates need at least a bachelor's degree, three or more years of manufacturing, quality control, or quality assurance experience, and knowledge of pharmaceutical characterization and analytical techniques. The position is based in Bend, Oregon, requires in-person attendance, and does not offer visa sponsorship.
