The Associate performs testing of in-process, final product, and stability samples in accordance with BMS policies, standards, procedures, and Global Regulatory and cGMP requirements. The role supports the Quality Control Analytical department at the Bristol Myers Squibb CAR T Manufacturing facility in Summit, New Jersey. The Associate may also support data verification and GMP documentation review as needed. The scheduled shift is Wednesday through Saturday, 6:30 a.m. to 4:30 p.m.
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Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree