Senior Specialist, Quality Control Analytical Testing

Purpose & Scope of Position

The QC Senior Scientist supports analytical testing in the QC Analytical Testing department at the CART manufacturing facility during clinical and commercial phases. Responsibilities include flow‑cytometry and molecular‑based testing for stability, validation, critical reagent qualification, training, and other critical support. The role requires independent task execution, interpretation of results, troubleshooting, and collaboration with multiple groups. Shift: Wednesday through Saturday, day shift.

• Advanced hands‑on experience with flow‑cytometry, molecular techniques, and pharmacological product characterization and transfer.
• Deep understanding of Global Regulatory and cGMP requirements.
• Strong technical writing, problem‑solving, and logical thinking.
• Ability to represent the group on cross‑functional teams and work independently in a high‑paced environment.
• Effective communication with peers, management, and cross‑functional stakeholders.

• Bachelor’s degree in a science discipline (advanced degree preferred).
• 2‑4 years of analytical testing or QC experience in a regulated setting.
• Experience with sterile cell culture, polychromatic flow‑cytometry panels, ELISA, and qPCR preferred.

• Perform cell‑based in‑vitro flow experiments, ELISA, and qPCR to assess critical reagent concentration.
• Handle complex issues and solve problems with general guidance.
• Prepare and present continuous‑improvement projects to management.
• Develop, write, and execute methods, protocols, reports, and related documents independently.
• Complete all work and peer‑review data within required timelines and cGMP standards.
• Review all data and documentation for compliance with applicable procedures.
• Assist with CAPA, deviation, project, and investigation/deviation tasks.
• Take leadership roles in projects when required.
• Draft and review technical documents such as SOPs, protocols, and reports.
• Communicate effectively with management regarding task completion, roadblocks, and needs.
• Maintain initiative, courage, and continuous improvement throughout investigative and corrective‑action life cycles.

• Must distinguish colors and have vision corrected to 20/20; annual eye exam required.
• Analyze numerical values on a daily basis.
• Laboratory setting, up to six hours per day, with exposure to biohazardous materials and chemical agents.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws. Recruitment and hiring practices are designed to ensure a diverse workforce and to provide reasonable accommodations for applicants with disabilities. Contact  for accommodations.

Requisition No.:

R1602459.