Serán BioScience

Quality Assurance Associate II/III (Swing Shift)

Bend, Oregon · Mid

No sponsorshipDetected 67 days ago

ComplianceGMP

About the 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.
Essential task include reviewing and approving production records, analytical data, and internal QA documentation.
Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections.

Serán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications.
We aim to build a workforce that is collaborative, creative, and kind.

In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture.

Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience.

Summary: Serán employees accrue over four weeks of paid time off annually.
Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period.
Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions.
Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage.
An Employee Assistance Program provides support for all things related to our employees' wellbeing, along with access to pet insurance.

Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.

Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

This listing is sourced directly from Serán BioScience's careers page and normalized into a canonical job model.