Quality Control Scientist I

Bend, Oregon April 8, 2026 Full Time

Serán is searching for an experienced Scientist to join our Quality Control team! The role of Scientist I supports the laboratory's ongoing sample testing performed by the Quality Control department in support of GMP practices and customer satisfaction. Successful candidates will demonstrate expertise with specific laboratory equipment, techniques, and methods for technical review and data analytics for the development and manufacturing of pharmaceutical therapies. The ideal education includes a Bachelors degree in Chemistry or another related field and 1-2 years post-graduation of hands-on instrumentation experience with a variety of analytical equipment within a GMP laboratory environment. Applicants without GMP or post-graduation experience are also encouraged to apply if they also have 2 years of lab experience.

At Serán we aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, employees approach their work with integrity and enthusiasm to promote a principled and positive work culture

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. 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.

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.

The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701

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

Duties and Responsibilities

Adheres to Standard Operating Procedures, cGMPs, Quality Manual, and company policies
Performs routine testing using analytical equipment including but not limited to HPLC, GC, KFC, Disso, etc.
Conducts appearance testing, raw materials sampling, solution preparation, and pH measurements
Drafts stability tables, sets-up stability studies, logs-in samples and standards
Cleans lab and glassware and disposes of analytical waste appropriately
Participates in process improvement and other non-routine projects
Conducts peer review of routine testing at the discretion of the relevant supervisor
Performs hypothesis testing or investigative work for OOS results under management and SME guidance
Demonstrates cross-functional support capabilities with other QC teams

Required Education and Experience

Bachelor’s degree in chemistry, physics, engineering, or related scientific discipline
Hands on lab experience
Communicates effectively and maintains productive relationships with coworkers, clients and other contacts outside the Company
Demonstrated ability to collaborate and work in cross-functional teams
Excellent organizational skills and attention to detail
Excellent time management skills with a proven ability to meet deadlines
Strong analytical and problem-solving skills
Ability to prioritize tasks and to delegate them when appropriate
Ability to function well in a high-paced and at times stressful environment
Proficient with Microsoft Office Suite or related software

Physical Requirements

Prolonged periods of sitting or standing at a desk and working on a computer

Prolonged periods of sitting or standing while monitoring laboratory equipment

Must be able to lift up to 15 pounds at times routinely, 30 pounds occasionally

Motor skills for basic laboratory operations

Adheres to consistent and predictable in-person attendance