Biotherapeutics Analytical Scientist – Methods & Data

RXinsider LTD.

Northern (KY)

Hybrid

USD 98,000 - 106,000

Full time

7 days ago
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Benefits offered by this job

Bonus/incentives based on performance
401K
Health and wellness coverage
Stock purchase program
Work life balance flexibility

Job summary

Charles River Biologics Testing Solutions seeks a scientist to assist in method development, validation, and routine testing of biotherapeutics in cGMP and R&D environments. You will interact with clients, interpret data, and deliver high-quality reports under supervision.

The role requires a chemistry/biotech background, 3+ years in CRO/pharma settings, and a strong grasp of regulatory requirements. Competitive pay and benefits accompany a collaborative, regulated work environment.

Qualifications

  • Bachelor’s degree in Chemistry/Biotechnology or related field; MS/PhD preferred.
  • Minimum 3 years of relevant CRO/pharma experience in characterization/analysis.
  • Equivalent mix of education and experience considered.

Responsibilities

  • Perform and troubleshoot analyses for biotherapeutics using analytical methods.
  • Execute chromatographic analyses and quantitative assays with high accuracy.
  • Interpret, present, and report data with minimal supervision.
  • Coordinate with clients on study design and timelines.
  • Maintain regulatory compliance and ensure safe, controlled lab operations.

Skills

Laboratory troubleshooting
Data interpretation
Report writing
Client interaction
Regulatory compliance
Team collaboration

Education

Bachelor's degree in Chemistry/Biotechnology or related scientific discipline
MS or PhD preferred

Tools

Empower software
Chromelion software

Job description

Charles River Biologics Testing Solutions seeks a scientist to assist in method development, validation, and routine testing of biotherapeutics in cGMP and R&D environments. You will interact with clients, interpret data, and deliver high-quality reports under supervision.

The role requires a chemistry/biotech background, 3+ years in CRO/pharma settings, and a strong grasp of regulatory requirements. Competitive pay and benefits accompany a collaborative, regulated work environment.

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