Associate Technical Writer - GMP Deviations & CAPA Support
Bristol-Myers Squibb
Bristol Myers Squibb seeks an associate to collaborate with internal Manufacturing partners, such as MSAT, Warehouse, Environmental Health and Safety (EHS) and Quality, to support improvement actions (Deviations, CAPAs, Change Control and Document updates). The associate will work with MO and Quality teams on CAPAs and Change Controls to ensure on-time implementation and maintain GMP documents for S12 CAR T manufacturing. #J-18808-Ljbffr Bristol-Myers Squibb
Vacancy posted 2 hours ago
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