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Bristol Myers Squibb
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New Brunswick, New Jersey
...
/working-with-us .
The CMC Regulatory Associate Director, Biologics is responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions to support
...
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Bristol Myers Squibb
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Princeton, New Jersey
...
/working-with-us .
The CMC Regulatory Associate Director, Biologics is responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions to support
...
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Bristol Myers Squibb
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Hyderabad,
India
...
/working-with-us .
The CMC Regulatory Associate Director, Biologics is responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions to support
...
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Bristol Myers Squibb
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Uxbridge,
United Kingdom
...
/working-with-us .
The CMC Regulatory Associate Director, Biologics is responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions to support
...
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Bristol Myers Squibb
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Hyderabad,
India
...
support Health Authority submissions. The team also supports Medical Information to build/maintain database to address external questions regarding drug products.
The CMC Regulatory Associate
...
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Bristol Myers Squibb
-
Princeton, New Jersey
...
support Health Authority submissions. The team also supports Medical Information to build/maintain database to address external questions regarding drug products.
The CMC Regulatory Associate
...
-
Bristol Myers Squibb
-
New Brunswick, New Jersey
...
support Health Authority submissions. The team also supports Medical Information to build/maintain database to address external questions regarding drug products.
The CMC Regulatory Associate
...
-
Bristol Myers Squibb
-
Uxbridge,
United Kingdom
...
support Health Authority submissions. The team also supports Medical Information to build/maintain database to address external questions regarding drug products.
The CMC Regulatory Associate
...
