Scientist, Analytical Science and Technology (ASAT), Cell Therapy

Scorpion Therapeutics; Seattle (WA); On-site; USD 110,000 - 170,000; Full time

Job summary

Bristol Myers Squibb is seeking a Scientist to support the Cellular Therapy product portfolio, focusing on bioassay, flow cytometry, and molecular biology methods for QC analytical support.

The role involves experimental work, data analysis, assay development/optimization, and potential leadership of investigations, with collaboration across regulatory and technical teams. Travel may be required.

Qualifications

• Bachelor's degree in a relevant scientific discipline; 6+ years in regulated environments, cellular or gene therapy.
• Experience with cell-based bioassays, flow cytometry, and molecular techniques.
• Preferred: advanced degree, experience with viral vectors (AAV, lentivirus), and cGMP compliance.
• HighValue: cellular/gene therapy, viral vectors, QC analytical methods, cGMP, regulatory compliance, FDA/EMA guidance.

Responsibilities

• Conduct experimental work and support method investigations.
• Analyze data and develop/optimize assays; assist in transfer and validation per regulatory standards.
• May lead projects, author technical documents, and support regulatory submissions.

Skills

Bioassay development

Flow cytometry

Molecular biology techniques

Data analysis

Education

Bachelor's degree in a relevant scientific discipline

MS/PhD preferred

Tools

Viral vectors (AAV, lentivirus)

cGMP experience

Job description

Role:

Scientist supporting Bristol Myers Squibb's Cellular Therapy product portfolio, focusing on bioassay, flow cytometry, and molecular biology methods for QC analytical support.

Responsibilities:

conduct experimental work, support method investigations, analyze data, develop and optimize assays, and assist in method transfer and validation in compliance with regulatory standards. May lead project and investigation tasks, author technical documents, and support regulatory submissions.

Requirements:

Bachelor's degree in a relevant scientific discipline; 6+ years of experience in regulated environments, cellular or gene therapy, with expertise in cell-based bioassays, flow cytometry, and molecular techniques. Preferred: advanced degree, experience with viral vectors (AAV, lentivirus), and cGMP compliance. HighValue: cellular/gene therapy, viral vectors, QC analytical methods, cGMP, regulatory compliance, experience with FDA/EMA guidelines.

Reporting:

reports to Cell Therapy Global Quality Analytical Sciences and Technology management.

WorkSetup:

not specified; travel may be required.