GMP QC Materials & Lab Documentation Specialist
Bristol Myers Squibb
Bristol Myer-Squibb in Summit, NJ seeks a Quality Control Raw Materials and Lab Support Specialist for a 12-month contract. Hybrid (50% onsite) with standard M-F hours, supporting CAR T manufacturing QC activities and GMP documentation. Requires 4+ years in a GxP environment and proven GMP writing experience. Role involves deviations, change controls, investigations, CAPA development, and collaboration with internal teams. Bachelors in Science required; pharma experience essential. #J-18808-Ljbffr Bristol Myers Squibb
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