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Bristol Myers Squibb
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Princeton LVL, New Jersey
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Director, Biologics is responsible for content development, compilation, maintenance, and review of the ... applications; New marketing applications; HA responses & background packages (including participating/leading
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Bristol Myers Squibb
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New Brunswick, New Jersey
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Director, Biologics is responsible for content development, compilation, maintenance, and review of the ... applications; New marketing applications; HA responses & background packages (including participating/leading
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Bristol Myers Squibb
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Princeton Pike, New Jersey
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Director, Biologics is responsible for content development, compilation, maintenance, and review of the ... applications; New marketing applications; HA responses & background packages (including participating/leading
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Takeda Pharmaceuticals
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Lexington, Massachusetts
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-changing therapies to patients worldwide.
Join Takeda as an Associate Director, Global Regulatory ... . Serve as or act as the delegate for the GRA CMC Product Lead at Regulatory, Pharmaceutical Development
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