Jobs / Serán BioScience / Quality Assurance Associate II/III

Quality Assurance Associate II/III

Serán BioScience
Bend, Oregon Onsite Quality Assurance Full-time Exempt
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About this role

Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. As a Quality Assurance Associate, you will be responsible for performing the day-to-day tasks of the QA Department supporting a GMP facility manufacturing and testing pharmaceutical products. Tasks include auditing and audit support, supplier quality management, and continuous improvement.  Additional responsibilities include Quality Management System, risk analyses, change management and investigations/CAPA. Preference will be given to candidates with Quality Assurance experience in the pharmaceutical industry, while those with Quality oversight experience are encouraged to apply.

About Serán BioScience

CDMO specializing in long-acting injectable formulations and polymer-based drug delivery. Based in Bend, OR.

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Job Details
PostedMay 22, 2026
LocationBend, Oregon
Work typeOnsite
DepartmentQuality Assurance
EmploymentFull-time Exempt
SeniorityMid
CountryUnited States
About the company
Serán BioScience
CDMO specializing in long-acting injectable formulations and polymer-based drug delivery. Based in Bend, OR.
View all 29 open jobs at Serán BioScience
BioHired Insights
Salary benchmark for Quality Assurance roles in United States: median 103,000 – 196,000 USD · based on 18 similar roles