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Merck
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Rahway, New Jersey
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the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and ... trials to world-wide regulatory application submissions and post marketing support.
The incumbent
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Merck
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Rahway, New Jersey
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Job Description
Position Description:
**Device Development Associate Principal
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L'Oreal USA
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Clark, New Jersey
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Home (https://careers.loreal.com/en_US/content/Home) / Job Search (https://careers.loreal.com/en\
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Organon & Co.
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Jersey City, New Jersey
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Background Packages, participating in Agency meetings on CMC topics, and executing global initial marketing
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Johnson & Johnson Consumer Inc
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Skillman, New Jersey
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culture in the R&D organization. You will work closely within R&D, marketing, Consumer Business
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Merck
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Rahway, New Jersey
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enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and ... objectives and meet worldwide regulatory and marketing needs.
Independently identifies and anticipates
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L'Oreal USA
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Clark, New Jersey
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, scientists, and business partners while serving as a primary point of contact and coordinator of novel and
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Oracle
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Trenton, New Jersey
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Job Description
Building off our Cloud momentum, Oracle has formed a new organization - Oracl
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J&J Family of Companies
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Skillman, New Jersey
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organization. You will work closely within R&D, marketing, Consumer Business Intelligence and other cross
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Oracle
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Trenton, New Jersey
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Job Description
Building off our Cloud momentum, Oracle has formed a new organization - Oracl
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L'Oreal USA
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Clark, New Jersey
...
Home (https://careers.loreal.com/en_US/content/Home) / Job Search (https://careers.loreal.com/en\
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Oracle
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Trenton, New Jersey
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Job Description
Building off our Cloud momentum, Oracle has formed a new organization - Oracl
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Colgate-Palmolive
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Piscataway, New Jersey
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& Support, Research & Implementation, Safety, Regulatory, Legal, Marketing) to review concepts/claims
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Merck
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Rahway, New Jersey
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the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and ... from individual clinical trials to world-wide regulatory application submissions and post marketing
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