Senior Scientist, Cell Therapy Analytics & QC Methods

Bristol Myers Squibb

Summit (NJ)

On-site

USD 108,000 - 131,000

Full time

9 days ago

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Benefits offered by this job

Comprehensive benefits
Flexible Time Off
11 paid holidays

Job summary

Bristol Myers Squibb in Summit, NJ seeks a Scientist to support the Cellular Therapy QC analytical methods, including bioassay, flow cytometry and molecular biology, with hands-on bench work and data interpretation.

You will design experiments, commit to regulatory requirements, train others, and partner with cross-functional teams to advance method lifecycle and method transfer during regulatory submissions.

Qualifications

  • Bachelor’s degree in a relevant scientific discipline; advanced degree preferred.
  • 8+ years of analytical experience in a regulated environment (GMP).
  • Hands-on lab experience with bioassays, flow cytometry, and molecular biology.

Responsibilities

  • Provide bioassay, flow cytometry, and/or molecular biology expertise for QC investigations.
  • Design, plan, and independently execute experimental work with data analysis and documentation.
  • Present experimental findings to the team and contribute to internal reports.
  • Support transfer of commercial methods and method validation per regulatory requirements.
  • Lead project, CAPA, and deviation/investigation tasks.
  • Train and mentor others in cell biology / molecular biology / flow cytometry techniques.

Skills

Bioassay
Flow cytometry
Molecular biology
Data analysis
Technical writing
Team collaboration
Regulatory knowledge

Education

Bachelor's degree
Advanced degree preferred

Job description

Bristol Myers Squibb in Summit, NJ seeks a Scientist to support the Cellular Therapy QC analytical methods, including bioassay, flow cytometry and molecular biology, with hands-on bench work and data interpretation.

You will design experiments, commit to regulatory requirements, train others, and partner with cross-functional teams to advance method lifecycle and method transfer during regulatory submissions.

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