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Scientist RSCR

Bristol Myers Squibb
September 16, 2026
Full-time
On-site
New Brunswick, NJ
Operations
Role: Support Reference Standard and Critical Reagent (RSCR) operations within biopharma programs, focusing on inventory management, laboratory activities, and project deliverables. Responsibilities: coordinate with project teams and stakeholders on supply, milestones, and operational priorities; prepare and review protocols, data, COAs, and documentation; execute routine inventory functions including labeling, tracking, and reconciliation; support sample scheduling, material tracking, and laboratory benchwork; ensure compliance with GxP, EHS, and quality standards; assist with reference standard qualification activities and operational issue resolution; contribute to continuous improvement initiatives. Requirements: BS or MS in biological sciences, chemistry, or related field; 0-5 years industry experience in biotech/pharma, with knowledge of biological and chemical analytical techniques, separation science, instrumentation, and bioanalytical methods; experience working with reference standards or critical reagents preferred. High-Value: biologics and small molecule programs, reference standards, GxP compliance, laboratory operations, biological and chemical analytical techniques. Work setup: onsite in New Brunswick, NJ, with up to 5% travel.