Senior Specialist, CAR-T Lifecycle Management

Role: Senior Specialist, CAR-T Lifecycle Management, supporting production of personalized cell therapy products for clinical trials and commercial supply at Bristol Myers Squibb. Responsibilities include providing process floor support, developing process automation inputs, managing technical projects, driving process improvements, and supporting regulatory inspections. The role involves cross-functional collaboration with Development, Manufacturing, Supply Chain, and Quality teams, with a focus on enhancing manufacturing strategies and resolving production issues. Qualifications: Bachelor's degree in science or engineering; 5+ years of cGMP experience in cell therapy; hands-on process engineering expertise; project management experience; familiarity with biopharma regulations and GxP standards. Preferred skills include knowledge of cell therapy manufacturing, single-use technologies, and ERP/MES systems; excellent organizational, communication, and strategic thinking abilities; experience with CAR-T or biopharmaceutical QC is a plus. High-Value: Cell therapy (CAR-T), biopharma manufacturing, process development, regulatory compliance, hands-on process engineering, cross-functional project management. Work setup: Hybrid (office and manufacturing/lab), with potential travel to NJ sites; flexible hours including some extended days and weekends.