Posted to MedZilla on 10/15/2018

Phaidon International

US-CA, Senior Regulatory Specialist 452431228202-MZ


 
 

A large medical device Company headquartered in the San Francisco bay area is looking for a Senior Regulatory Affairs Specialist.  This position offers great compensation, benefit packages, and unprecedented growth opportunities with an industry leader.

 

We are looking for a professional that can lead preparation of regulatory submissions, submit regulatory documents such as safety reports and license renewals to clinical trials, and be responsible for ensuring product packaging and associated information in accordance to licensure. 

 

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 (micro biology, chemistry, biology) or higher
  • At least 2-3 years of regulatory experience
  • Must have experience GXPs (GMPs, GLPs, GCPs)
  • Knowledge of international and domestic submission requirements
  • Great written and verbal communication skills
 

Responsibilities:
  • Identify new, and enhance old regulatory policies
  • Develop regulatory strategies based upon regulatory changes
  • Develop SOPs
  • Write and edit technical documents

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.