Flow Cytometry Scientist – Immunotox Data and Analysis

Charles River Laboratories

Mattawan (MI)

On-site

USD 48,000 - 80,000

Full time

13 days ago
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Benefits offered by this job

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

Job summary

Charles River Laboratories is seeking a skilled scientist in the Immunotox group to support drug development by performing immune response analyses and cell-based assays. You will develop, validate, and analyze data across regulated and non-regulated non-clinical studies.

The role emphasizes project portfolio management, data integrity, and collaboration with sponsors, with the goal of timely, high-quality results.

Qualifications

  • Bachelor’s degree in life sciences with 5–7 years relevant experience, or Master’s with 1–2 years, or PhD with no experience.
  • Strong verbal and written communication abilities across levels.
  • Proficiency with Microsoft Office; ability to learn validated systems.

Responsibilities

  • Manage a portfolio of sample analysis projects and meet timelines.
  • Review and approve data; support scientific/technical decisions.
  • Assist with quality audits and investigations; respond to QA observations.
  • Write study plans/protocols/amendments with guidance.
  • Communicate with sponsors and internal teams; ensure data integrity.
  • Develop and validate quantitative/qualitative methods under scope.
  • Perform data analysis using appropriate software.

Skills

Communication skills
MS Office
Validated systems
Extended hours availability
Team collaboration
US work authorization

Education

Bachelor’s degree in life sciences
Master’s degree in life sciences
PhD in life sciences

Tools

Data analysis software

Job description

Charles River Laboratories is seeking a skilled scientist in the Immunotox group to support drug development by performing immune response analyses and cell-based assays. You will develop, validate, and analyze data across regulated and non-regulated non-clinical studies.

The role emphasizes project portfolio management, data integrity, and collaboration with sponsors, with the goal of timely, high-quality results.

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