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 Regulatory Affairs Consultant

Details
Country: USA
Location: New Jersey-Northern US-NJ-Northern
Total applied: 1
Job Category:Biotech/R&D/Science
Location:US-NJ-Northern
Status:Full Time, Temporary/Contract/Project, Employee
Regulatory Affairs Consultant

 

Regulatory Affairs Consultant

 

Our client has a high priority need in its Regulatory Affairs group for a Regulatory Affairs Consultant in its Northern NJ location.  This is a great opportunity that offers potential for you to leverage your experience and while working with a top-notch team.

 

In this position, you will play an integral role in Regulatory Affairs.  Experience doing FDA and EU submissions, Regulatory Strategy, Project Management is required. 5 years of Regulatory Affairs experience needed. 

 

Experience in a Project setting is desirable.  Take advantage of this great opportunity to expand on your Project Management skills and increase your potential in the ever expanding Regulatory marketplace.

 

Your day-to-day responsibilities will be directly determined not only by your previous experience, but also by your desire to take on challenges.  If you have experience in some of these areas and are looking to round out your arsenal, we would be interested in speaking with you about this position. 

 

*** NOTE: We have requirements for similar opportunities (both permanent and contract) in other locations around the country, and for client projects in Europe.  If you have expertise in Regulatory Affairs or Regulatory Operations and would be interested in discussing available opportunities (either permanent or contract positions), please contact jbogdansky@kleinhersh.comto discuss. ***

 

Visit www.kleinhersh.com to view additional job opportunities available through our company.

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