Posted to MedZilla on 10/23/2017


Phaidon International

US-CA, Senior Regulatory Specialist 452431227043-MZ


 
 

One of the largest and industry leading medical device companies headquartered in Los Angeles, CA is looking for a Sr. Regulatory Affairs Specialist.  This position offers great compensation, benefit packages, and unprecedented growth opportunities.

We are looking for a professional that can provide support to ensure efficient business processes and environment. Someone who can assist in SOP development and review, as well as have regulatory input in product life cycle 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 degree or higher in related scientific background (biology, micro biology, medical technology, pharmacy, pharmacology, math, engineering)
  • At least 2-3 years of regulatory experience
  • Must have experience in GCPs, GLPs, and GMPs
  • Knowledge of domestic and international regulatory guidelines and policies
  • Great written and verbal communication skills
 
Responsibilities:
  • Identify new, and enhance old regulatory policies
  • Develop regulatory strategies based upon regulatory changes
  • Working with requirements of advertising, promotion, and labeling
  • Working with cross functional teams

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.