Senior Scientist, Cell Therapy Analytics & Bioassays

Bristol-Myers Squibb Co; Madison (NJ); On-site; USD 108,000 - 131,000; Full time

Benefits offered by this job

Flexible Time Off

Comprehensive benefits

11 paid company holidays

Job summary

Bristol Myers Squibb is seeking a Senior Scientist, Drug Product Analytical Sciences (ASAT) in Cell Therapy to design, execute and interpret analytical experiments for QC methods. The role focuses on bioassay, flow cytometry and molecular biology analyses and requires hands-on bench work and cross-functional collaboration.

The candidate will contribute to method development, validation and regulatory-driven submissions, while mentoring teammates and ensuring cGMP compliance across projects.

Qualifications

• Bachelor’s degree in relevant scientific discipline; advanced degree preferred.
• 8+ years of analytical experience in GMP, cellular therapy, or gene therapy.
• Experience with bioassay, flow cytometry, and molecular biology methods.

Responsibilities

• Provide bioassay, flow cytometry and/or molecular biology analytical expertise in QC investigations.
• Design, plan and independently execute experimental work with high technical proficiency; contribute to data analysis and reports.
• Support transfer of commercial methods and method validation per global regulatory requirements.
• Train and mentor others; champion quality culture; lead improvement efforts.

Skills

Bioassay

Flow cytometry

Molecular biology

Technical writing

Education

Bachelor's degree in relevant field

Advanced degree preferred

Tools

GMP experience

Job description

Bristol Myers Squibb is seeking a Senior Scientist, Drug Product Analytical Sciences (ASAT) in Cell Therapy to design, execute and interpret analytical experiments for QC methods. The role focuses on bioassay, flow cytometry and molecular biology analyses and requires hands-on bench work and cross-functional collaboration.

The candidate will contribute to method development, validation and regulatory-driven submissions, while mentoring teammates and ensuring cGMP compliance across projects.