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Biophysicist Surface Plasmon Resonance

Location: 

Leadville, Colorado, US

Type of contract:  Permanent
Posting date:  Jan 23, 2026
Job offer reference:  201468

Overview:
Business Title: Biophysicist Surface Plasmon Resonance
Position Title: Scientist I
Division: Consumer Products Services 
Entity: ATL
Location: Louisville, CO
Reports to: Manager
FLSA: Non-exempt
 
Hours Worked: Typically, Monday through Friday 8:00 AM – 4:30 PM. However, must be flexible to work overtime as needed.

 

Position Summary:
The Biophysicist, Surface Plasmon Resonance is responsible for hit-to-lead discovery efforts by employing multiple technologies to characterize small molecule-protein, protein-protein, and other complex interactions. 

Duties and Responsibilities:
It is everyone’s responsibility to live out our Values and Absolutes by Shaping a World of Trust while ensuring responsible progress.
•    Characterize protein-ligand and protein-protein interactions primarily by SPR (Surface Plasmon Resonance). However, a variety of methods may also be used including but not limited to; Bio Layer Interferometry (BLI), fluorescence spectroscopy, light scattering techniques, intact protein mass spectrometry, and DSF.
•    Biophysically characterize protein samples destined for multiple workflows.
•    Use biophysical tools to interrogate protein-ligand and/or protein-protein interactions to triage or advance compound or large molecule series.
•    Learn and develop technical expertise in protein biochemical and biophysical characterization across multiple platforms which may lay outside the current skill set.
•    Develop and continually advance one’s knowledge base on genetically targeted drugs and structure-based drug design.
•    Adapt to highly dynamic project priorities, with diligent and rapid communication of scientific results and insights to the team, including maintaining an ELN and uploading data to the database.
•    Perform work in compliance with company Research Policies.
•    Perform final review and interpret data / reports. Perform critical error review. 
•    Review and close root cause analysis and corrective actions. 
•    Works directly with external contacts to implement new testing or process initiatives. 
•    Assist in the coordination of technical & administrative aspects of various departmental projects, providing direction to techs. 
•    Perform background/literature research to help further research goals. 
•    Conduct operational audits to identify defects and inconsistencies. 
•    Reviews contract requirements prior to testing in order to assure adherence to client requirements, and coordinates testing between labs. 
•    Perform final review and interpret data / reports for external regulatory agencies. 
•    Write, implement and update SOPs, test protocols, and technical procedures to facilitate department development and improve quality. 
•    Method development – write and adapt custom methodology for custom materials
•    Follow the guidelines set forth with clients and in the Bureau Veritas Consumer Products Services, Inc Quality, Health, Safety, Security and Environmental policies and procedures. 
•    Comply with clients and Bureau Veritas Consumer Products Services, Inc management systems in accordance with appropriate regulatory agencies. 
•    Follows the guidelines set forth in by clients and the Bureau Veritas Consumer Products Services, Inc Quality Manual and Safety / Chemical Hygiene Plan. 
•    Other duties as defined by Manager, department needs and workload. 

Skills & Proficiencies:

•    Direct experience in large or small molecule assay development for SPR.
•    Chemical labeling methods and technologies.
•    Experience using automation technologies (e.g. SPT Labtech, Tecan) programming and method development.
•    Experience in fluorescent-based methods or assay development (e.g. FP, FRET, etc.).
•    Working knowledge in assay development and utilizing BLI (e.g. Octet) and method development
•    Committed to staying current with the latest scientific breakthroughs in structure-based drug design and biophysical analysis.
•    Highly organized with excellent analytical, documentation and multi-tasking skills.
•    Proven ability to work in a flexible, team-oriented environment.
•    Excellent interpersonal skills with the ability to communicate and interact well with colleagues at all levels.
•    Full method development skills 
•    Champions Company Values


Education and Experience:
•    Bachelor’s of Science in Biochemistry, Chemical Biology, or a related field.
o    Master’s Degree preferred
•    2+ years of hands-on experience with SPR (e.g. Biacore, Bruker, or Caterra) and sound knowledge of various immobilization techniques. 

 

Compensation Range: $45.00-$51.00 per hour  (e.g., the job posting is not necessarily reflective of actual compensation that may be earned, and actual compensation is subject to variation due to such factors as locations, education, experience, and skillset).

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