Job Title: QC Scientist

Job Description

When you are part of the team, you’ll do important work and have the opportunity for continual growth and learning in a culture that empowers your development. As part of the Quality Control Biochemistry Group, you directly impact patients’ lives by providing testing to ensure their biologic pharmaceuticals are safe and potent!

Work Location: St. Louis, MO (on-site)

What will you do?

• Conduct routine compendial, purity, and impurity testing of pharmaceutical release, stability, and in-process samples by internally developed, qualified, and validated test methods.

• Support qualification and validation of test methods for pharmaceutical concentration, purity, and impurity testing.

• Assist in preparing regulatory documents and other communications with outside agencies, clients, and/or colleagues from other corporate sites.

• Perform all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Maintain the necessary compliance status required by company and facility standards.

Skills

• cGE (capillary gel electrophoresis) experience from school or 6 months-1 year of industry (example: MS Level Biochemist with cGE)
• Minimum of 1 year of cGE-icIEF experience in quality/analytical/pharmaceutical industry or similar experience
• Knowledge of GMP regulations in cGMP manufacturing environment
• Working knowledge of scientific principles for wide range of analytical techniques

Work Environment

Friday-Monday role, 10 hour Shift (Must be flexible for 8-6pm, 10-8pm, and 12-9pm)

Bench work