GMP QA Associate II — Clinical Manufacturing
Listed on 2026-10-17
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Serán Bioscience, LLC in Bend, Oregon, is hiring a Quality Assurance Associate to ensure regulatory compliance in drug manufacturing. Key responsibilities include reviewing SOPs and production records, managing audits, and oversight of investigations. Candidates should have GMP experience and a bachelor’s degree in a scientific field.
Benefits include more than four weeks of paid time off and employer contributions to retirement accounts. Applicants must be authorized to work in the U.S. as sponsorship is not available.
Consider building your career as a GMP QA Associate II — Clinical Manufacturing at Serán Bioscience, LLC.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Bend, OR, United States.
This opportunity is part of our work in Management & Operations.
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