HPLC Scientist – Analytical Development HPLC Scientist – Analytical Development Eurofins In-per[...]

Seeds Renewables; Lexington (KY); On-site; USD 70,000 - 90,000; Full time

Job summary

A biotechnology company in Kentucky seeks an HPLC Scientist to join its analytical development team. The role involves executing testing and analytical development for biological therapeutic products while ensuring compliance with regulatory requirements. Key responsibilities include performing techniques such as HPLC and capillary electrophoresis, as well as data analysis and troubleshooting methods. Strong analytical skills and experience with cGMP/GLP guidelines are essential.

Qualifications

• Experience in bioanalytical methods such as HPLC and UPLC.
• Knowledge of relevant regulatory requirements (cGMP/GLP).
• Strong analytical skills with ability to interpret complex data.

Responsibilities

• Execute analytical development and routine testing.
• Perform data analysis and documentation.
• Troubleshoot HPLC, UPLC, and CE methods.

Skills

HPLC/UPLC

Capillary Electrophoresis

Data Analysis

Problem Solving

Job description

HPLC Scientist – Analytical Development

The Analyst Scientist will contribute as part of an analytical development team supporting biological therapeutic product release and characterization testing in a regulated, compliance-based environment.

Key responsibilities include:

• Execute analytical development and routine testing using established methods to support biologics characterization and release testing.
• Independently perform techniques including but not limited to:
  • HPLC/UPLC (SEC, CEX, Reverse Phase)
  • Capillary Electrophoresis (CE, CE‑SDS)
  • icIEF (Maurice), iCE
  • P20, P80 methods
• Perform data analysis, interpretation, and documentation in accordance with approved test methods, protocols, and reporting requirements.
• Troubleshoot HPLC, UPLC, and/or CE methods and instrumentation as needed.
• Apply sound scientific judgment in technique selection, method execution, and problem‑solving for assignments of moderate scope and complexity.
• Conduct all work in compliance with cGMP/GLP, safety policies, and regulatory requirements.
• Support non‑laboratory tasks as assigned (e.g., documentation support, data review, presentations).