Bioanalytical Development Associate II

KBI Biopharma

Durham (NC)

On-site

USD 55,000 - 75,000

Full time

6 days ago
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Job summary

KBI Biopharma, Inc. in Durham, NC, is seeking a Research Associate II to join the Analytical Development Department.

You will execute experimental protocols, perform elementary data analysis, and collaborate with your manager to meet project goals in a highly technical environment. Responsibilities include conducting bio-analytical testing (HPLC, SDS-PAGE, ELISA, UV-Vis), maintaining notebooks, analyzing results, staying current with literature, and following safety procedures.

Qualifications

  • Bachelor's degree in chemistry or biochemistry or related area; 2–4 years of experience.
  • Ability to read, analyze, and interpret general business periodicals, journals, and procedures.
  • Ability to write reports and present information to groups of managers and clients.
  • Ability to apply logical/scientific thinking to problems and handle complex variables.

Responsibilities

  • Performs testing on drug substance/drug product, or formulation samples using bio-analytical techniques (HPLC, SDS-PAGE, SDS-CGE, ELISA, UV-Vis, etc.).
  • Makes detailed observations and carries out elementary data analysis.
  • Understands experiments and conducts troubleshooting analyses.
  • Maintains and updates knowledge of instrumentation and lab notebooks.
  • Adheres to safety requirements and proper labeling/handling of hazardous waste.

Skills

Analytical thinking
Scientific literacy
Strong communication skills
Problem solving
Data interpretation

Education

B.A./B.S. degree in chemistry or biochemistry

Tools

HPLC
SDS-PAGE
SDS-CGE
ELISA
UV-Vis

Job description

KBI Biopharma, Inc. in Durham, NC, is seeking a Research Associate II to join the Analytical Development Department.

You will execute experimental protocols, perform elementary data analysis, and collaborate with your manager to meet project goals in a highly technical environment. Responsibilities include conducting bio-analytical testing (HPLC, SDS-PAGE, ELISA, UV-Vis), maintaining notebooks, analyzing results, staying current with literature, and following safety procedures.

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