GLP Analytical Chemistry Research Scientist

Charles River Laboratories; Reno (NV); On-site; USD 90,000 - 95,000; Full time

Benefits offered by this job

Bonus incentives

401K matching

Paid time off

Stock purchase program

Health coverage

Wellbeing programs

Work-life balance

Job summary

Charles River Laboratories seeks an experienced Research Scientist (Analytical Chemistry) for our Safety Assessment site in Reno, NV. The role involves conducting preclinical studies, GLP-compliant study management, data interpretation, and reporting with expert use of techniques like HPLC and iCIEF.

You'll coordinate study planning across departments, prepare high-quality protocols and reports, and interact with sponsors for scheduling and study execution.

Qualifications

• Bachelor's degree or higher in a scientific discipline with 3–5 years of related experience.
• Expertise in analytical techniques (HPLC, SoloVPE, UV-Vis, CE, iCIEF) and GLP awareness.
• Strong data interpretation, reporting, and study management skills.

Responsibilities

• Conduct preclinical and clinical studies with basic to moderate complexity, ensuring regulatory compliance.
• Serve as study director for assigned studies under GLP regulations.
• Coordinate study planning with departments and generate protocols/reports.
• Interpret and present data; provide technical guidance to staff.
• Interact with sponsors on planning, scheduling, and reporting of studies.

Skills

HPLC

SoloVPE

UV-Vis

Subvisible particles

CE

iCIEF

Regulatory compliance

Education

Bachelor's degree in a scientific discipline

Master's degree or PhD preferred

Tools

Microsoft Excel

Microsoft Word

PowerPoint

Job description

Charles River Laboratories seeks an experienced Research Scientist (Analytical Chemistry) for our Safety Assessment site in Reno, NV. The role involves conducting preclinical studies, GLP-compliant study management, data interpretation, and reporting with expert use of techniques like HPLC and iCIEF.

You'll coordinate study planning across departments, prepare high-quality protocols and reports, and interact with sponsors for scheduling and study execution.