Posted to MedZilla on 12/13/2017


Phaidon International

US-CA, Senior Regulatory Affairs Specialist 452431229515-MZ


 
 

A growing medical Device Company headquartered in the South San Francisco bay area is looking for a Senior Regulatory Affairs Specialist.  This position offers unprecedented growth opportunities, benefits package, and competitive salary.

 

We are looking for a professional that can provide a team with strategic planning and assist with SOP development, as well as provide input on regulatory lifecycle planning.   

 

If interested and would like more information on this position, please feel free to send me your up to date resume and cover letter to [click here]">[click here].

 

Requirements:
  • Bachelors  in biology, micobiology, chemistry, or related meidical fields
  • Masters in regulatory affairs preferred but not required
  • At least 2-5 years relevant regulatory experience in the medical device industry
  • Knowledge of FDA regulatory requirements
  • Great written and verbal communication skills
 

Responsibilities:
  • Understand submission and registration types (GXPs)
  • Must be able to execute regulatory strategy to obtain approvals
  • Understand international and domestic regulatory guidlines and regulations
  • Understand and be able to implement medical writing, labeling,and advertising promotion

Please visit our website at www.phaidoninternational.com

 
 


* If a direct employer requests that you go to their web site and complete your application there in order to be
  considered, please do so. Applications for all positions are subject to each employer's specific requirements.