Regulatory Specialist

 
Location: Tennessee Ridge, Tennessee
Posted On: 8/5/2017
Job Code: 7460_RAS_TN_MP
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Job Description
 
The Associate Regulatory Affairs Specialist is responsible for coordinating and preparing International submissions related to our medical devices.

POSITION RESPONSIBILITIES:
• Coordinate and prepare product documentation for International regulatory agencies.
-Coordinate and consult with other departments on the content, review and assembly of regulatory documentation.
-Maintain the electronic/paper regulatory archives for all projects.

In order to be considered for this position, the following basic qualifications must be evident on your resume

Bachelors or Masters degree with:
• 2-4 Years regulatory experience with Bachelors
• 0-2 Years regulatory experience with Masters

DESIRED/PREFERRED QUALIFICATIONS
• Computer software applications including knowledge of MS Office (strong Excel skills desired), Documentum, SAP
• Strong communication skills
• Results oriented focus
• Ability to work independently and support multiple projects
• International Regulatory Medical Device experience
Category:Non-IT  code:new
 
 
Job Requirements
 
 
SAP,Regulatory,Regulatory Affairs
 

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Contact Details
 
Recruiter
Sparsh Patel
 
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E-mail Address
 
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