Quality Control Scientist II - In-Process Lab & HPLC

Serán BioScience; Bend (OR); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Paid time off: 4+ weeks

Retirement plan after 90 days

Health insurance options

Employee Assistance Program

Job summary

Serán BioScience in Bend, Oregon is seeking an experienced Quality Control Scientist II to support an extended manufacturing schedule and ensure manufacturing excellence through rigorous testing in a cGMP laboratory.

The role emphasizes in-process control methods, data integrity, and cross-functional collaboration within QC teams, with a preferred 11:00 am–8:00 pm schedule (negotiable for swing shifts).

Qualifications

• Bachelor’s degree in a scientific discipline or related field.
• Minimum 3 years of dedicated lab experience.
• Requires 2 years of GMP experience.

Responsibilities

• Adheres to SOPs, cGMPs, Quality Manual and policies.
• Performs routine extractions for dissolution, assay and impurities testing.
• Operates analytical equipment (including HPLC) and manages data records.
• Conducts appearance testing, sampling, solution prep and pH measurements.
• Prepares stability tables and runs stability studies.
• Cleans lab, glassware and disposables, handles waste per procedures.
• Supports process improvement and non-routine projects.
• Performs peer review of routine testing as directed.
• Assists in investigating OOS results under guidance.
• Trains and mentors staff on processes and procedures.
• Demonstrates cross-functional support with QC teams.
• Duties may expand with company initiatives.
• Performs other related duties as assigned.

Skills

HPLC experience

Cross-functional teamwork

Analytical instrumentation

Attention to detail

Microsoft Office

Empower software

Education

Bachelor’s degree in a scientific discipline

Tools

Empower

Job description

Serán BioScience in Bend, Oregon is seeking an experienced Quality Control Scientist II to support an extended manufacturing schedule and ensure manufacturing excellence through rigorous testing in a cGMP laboratory.

The role emphasizes in-process control methods, data integrity, and cross-functional collaboration within QC teams, with a preferred 11:00 am–8:00 pm schedule (negotiable for swing shifts).