Posted to MedZilla on 10/16/2017


Phaidon International

US-CA, Regulatory Specialist 452431227836-MZ


 
 

A medical device start up headquartered in the Los Angeles greater area is looking for a regulatory specialist.  This position offers great compensation, benefit packages, and unprecedented growth opportunities with an up and coming company.

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 or higher in related scientific background (MS, PhD is highly preferred)
  • At least 3-5 years of regulatory experience
  • Must have experience in 510K, PMA, and IVDs
  • Knowledge of QA/QC systems for clinical and commercial products
  • Great written and verbal communication skills
 

Responsibilities:
  • Identify new, and enhance old regulatory policies
  • Develop regulatory strategies based upon regulatory changes
  • Understanding of QA systems
  • Manage doucument submissions
 


Please visit our website at www.phaidoninternational.com

 
 


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  considered, please do so. Applications for all positions are subject to each employer's specific requirements.