Analytical Scientist, LC-MS & Protein Analytics

KBI Biopharma, Inc.; Louisville (CO); On-site; USD 85,000 - 125,000; Full time

Job summary

KBI Biopharma, Inc. seeks an analytical scientist to join the Characterization Services team in Louisville, CO.

The role focuses on protein analytics using LC-MS, with responsibilities spanning method development, analytical testing for development through regulatory submission, and documentation for regulatory review. Strong communication and collaboration are essential in a fast-paced, team-driven environment.

Qualifications

• BS, MS, or Ph.D. in Biophysics, Biochemistry, Analytical Chemistry, Biochemical Engineering
• BS with 7 years of relevant experience
• MS with 5 years of relevant experience
• Ph.D. with relevant experience
• Excellent communication skills and ability to present complex data to diverse audiences
• Proficiency in scientific software and data analysis tools
• Ability to work independently and collaboratively in a fast-paced environment

Responsibilities

• Demonstrate expertise in LC-MS, HPLC/UPLC, and other common analytical techniques
• Provide method development support in addition to adhering to established methods for client programs
• Execute analytical experiments in support of product development and regulatory submissions
• Generate high-quality documentation of experiments suitable for publication and regulatory review
• Perform peer reviews of data documented in ELNs and reports
• Glycan characterization experience is preferred but not required

Education

BS/MS/PhD in Biophysics, Biochemistry, Analytical Chemistry, Biochemical Engineering

BS with 7 years of relevant experience

MS with 5 years of relevant experience

Ph.D. with relevant experience

Tools

Scientific software

Job description

KBI Biopharma, Inc. seeks an analytical scientist to join the Characterization Services team in Louisville, CO.

The role focuses on protein analytics using LC-MS, with responsibilities spanning method development, analytical testing for development through regulatory submission, and documentation for regulatory review. Strong communication and collaboration are essential in a fast-paced, team-driven environment.