GMP QC Scientist – Lab Testing & Data Analysis

Serán BioScience; Bend (OR); In loco; USD 70.000 - 100.000; Tempo pieno

Vantaggi offerti da questo lavoro

PTO accrual

Retirement plan (5% 401k)

Health plans

Life and disability coverage

Employee assistance program

Descrizione del lavoro

Serán BioScience in Bend, Oregon seeks a scientist with laboratory experience to support manufacturing in In-Process Control within GMP environments. You will test raw materials and production equipment, review data, and contribute to technical investigations to ensure high-quality drug products.

Preferred candidates have cGMP experience and strong written and verbal communication. The role emphasizes collaboration with QC teams, data analysis, and involvement in process improvements in a

Competenze

• Bachelor's degree in a related scientific discipline is required.
• 3 years of hands-on laboratory experience; cGMP experience preferred.
• Minimum 2 years of GMP experience to be considered for Scientist II.

Mansioni

• Adheres to SOPs, cGMPs, Quality Manual, and company policies.
• Performs routine testing using analytical equipment including HPLC, GC, TOC, FT-IR.
• Conducts appearance testing, solution preparation, raw material sampling, and pH measurement.
• Drafts stability tables, sets up stability studies, logs samples and standards.
• Cleans lab and glassware and disposes of analytical waste appropriately.
• Performs technical writing and reporting including incident reporting and investigations.
• Supports cross-functional QC teams and participates in process improvement initiatives.

Conoscenze

HPLC

GC-HS

TOC

FT-IR

Raw materials testing

Cross-functional collaboration

Written communication

Formazione

Bachelor's degree in related scientific discipline

Strumenti

Microsoft Office Suite

Descrizione del lavoro

Serán BioScience in Bend, Oregon seeks a scientist with laboratory experience to support manufacturing in In-Process Control within GMP environments. You will test raw materials and production equipment, review data, and contribute to technical investigations to ensure high-quality drug products.

Preferred candidates have cGMP experience and strong written and verbal communication. The role emphasizes collaboration with QC teams, data analysis, and involvement in process improvements in a