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Quality Assurance Associate II/III -Quality Management System

SeranbioBend🇺🇸United StatesPosted May 22, 2026

Quick overview

SeniorityMid Senior
Employment typeFull Time
Work modeOn Site
LocationBend, United States
Posted5 months ago
Document Management

Job description

Serán BioScience is searching for an experienced Quality Assurance Associate to support quality systems programs. As a Quality Assurance Associate, you will be responsible for performing the day-to-day tasks of the QA Department in a GMP facility manufacturing pharmaceutical products. Tasks include supporting quality system programs such as document management, training, and quality event programs.  Additional responsibilities include assisting in the maintenance of the electronic Quality Management System, conducting risk analyses and investigations, and participating in audits and inspections. Preference will be given to candidates within the pharmaceutical industry, while those with Quality oversight experience encouraged to apply.