Senior Scientist, Cell Therapy Analytics & QC

Nutanix

Seattle, Northern (WA, KY)

Hybrid

USD 117,000 - 142,000

Full time

8 days ago
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Job summary

Bristol Myers Squibb in Seattle, WA is seeking a Senior Scientist in Drug Product Analytical Science (ASAT) for Cell Therapy. The role will conduct bench experiments and provide analytical expertise in bioassay, flow cytometry and molecular biology to support QC investigations.

You will design experiments, analyze data, and contribute to method transfer, validation, and regulatory submissions while training team members and guiding cross-functional projects in a fast-paced biotherapeutics

Qualifications

  • Bachelor's degree or higher in a relevant science field with GMP exposure.
  • 8+ years of analytical experience in cellular therapy or GMP environments.
  • Expertise in bioassay, flow cytometry or molecular biology methods.

Responsibilities

  • Provide bioassay, flow cytometry and/or molecular biology analytical expertise in QC investigations.
  • Design, plan and execute experimental work; contribute to data analysis and documentation.
  • Support transfer of commercial methods, validation, and regulatory reporting.
  • Lead project, CAPA and deviation/investigation tasks and drive improvements.
  • Train and mentor others in cell biology, molecular biology and flow cytometry.

Skills

Bioassay
Flow cytometry
Molecular biology
GMP
Regulatory knowledge
Technical writing
Data analysis
Laboratory techniques

Education

Bachelor’s degree in a relevant scientific discipline or equivalent
Advanced degree preferred

Tools

Lentiviral vectors
AAV vectors
Regulatory documentation tools

Job description

Bristol Myers Squibb in Seattle, WA is seeking a Senior Scientist in Drug Product Analytical Science (ASAT) for Cell Therapy. The role will conduct bench experiments and provide analytical expertise in bioassay, flow cytometry and molecular biology to support QC investigations.

You will design experiments, analyze data, and contribute to method transfer, validation, and regulatory submissions while training team members and guiding cross-functional projects in a fast-paced biotherapeutics

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