Posted to MedZilla on 4/30/2017


Phaidon International

US-CA, Director of Regulatory Affairs 452431224013-MZ


 
 

Global medical device Company headquartered in San Francisco, California is looking for a Director of Regulatory Affairs.  This position offers great compensation, benefit packages, and unprecedented growth opportunities.

We are looking for a professional that can lead preparation of regulatory submissions, develop strategy, submit regulatory documents such as safety reports and post-market products support and license renewal. 

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 or higher in related scientific background (PhD highly preferred)
  • At least 10-15 years of regulatory experience
  • Must have experience with PMAs, 510k, and IVDs
  • Knowledge of FDA and Health Canada regulatory practices
  • Must have Reagent and chemical experience
 

Responsibilities:
  • Able to advise sales, marketing, clinical, and R+D groups in regulatory areas
  • Prepare and maintain SOPs
  • Being able to work in U.S. and Japanese markets
  • Able to lead marketing and sales strategy

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.