Entry-Level Laboratory Research Analyst

Charles River Laboratories, Inc.

Michigan

On-site

USD 27,000 - 38,000

Full time

16 hours ago
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Benefits offered by this job

Bonus incentives
401K
Paid time off
Stock purchase program
Health coverage
Wellbeing programs
Work-life balance

Job summary

Charles River Laboratories, Inc. is seeking an entry-level Research Analyst I to support regulated and non-regulated preclinical and clinical studies.

You will execute laboratory procedures, perform analyses, validate methods, and assist with formulation activities across several disciplines while adhering to GxP, SOPs, and quality standards. The role emphasizes attention to detail, organization, and the ability to work in a fast-paced, deadline-driven environment.

Qualifications

  • Bachelor's degree in biology, chemistry, biochemistry, molecular biology, pharmacy, immunology, or related field.
  • No professional experience required; relevant academic lab experience preferred.
  • Experience with LC/MS/MS, qPCR, ddPCR, flow cytometry, cell culture or formulation preparation is preferred.

Responsibilities

  • Perform and document laboratory procedures, materials, and results in compliance with SOPs and regulatory standards.
  • Maintain accurate, timely laboratory documentation and data recording.
  • Communicate effectively with peers, supervisors, and project teams.
  • Assist with laboratory maintenance, organization, and inventory.
  • Support routine sample analysis and method development/validation projects.
  • Operate instruments and analyze data using validated software systems.

Skills

Attention to detail
Organizational skills
Verbal & written communication
Microsoft Office
Analytical thinking
Time management
Teamwork

Education

Bachelor's degree in a related scientific discipline

Tools

LC/MS/MS
qPCR
ddPCR
Flow cytometry
Cell culture
Formulation preparation

Job description

Charles River Laboratories, Inc. is seeking an entry-level Research Analyst I to support regulated and non-regulated preclinical and clinical studies.

You will execute laboratory procedures, perform analyses, validate methods, and assist with formulation activities across several disciplines while adhering to GxP, SOPs, and quality standards. The role emphasizes attention to detail, organization, and the ability to work in a fast-paced, deadline-driven environment.

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