Pharma Documentation & Change Control Specialist
Bristol Myers Squibb
Bristol Myers Squibb in New Jersey is seeking a professional to manage commercial specifications and methods ensuring compliant documentation across drug products and materials. The role focuses on content review of change controls, global testing standards, and QC documents. The candidate should have a bachelor's degree, at least four years in pharma, and experience with SAP or LIMS, with strong communication and project management skills to collaborate across R&D, Regulatory, IT and QA. #J-18808-Ljbffr Bristol Myers Squibb
Vacancy posted 1 day ago
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