Posted to MedZilla on 6/10/2017


ProClinical

US-Northeast, Regulatory Affairs Specialist


 
 

1 Year contract assignment in a Regulatory Affairs Specialist role with one of our largets clients.

Location: Raynham(MA), Warsaw (IN), Somerville(NJ)

Requirements:

- Experience writing design dossiers

- Experience updating tech files

- Strong working FDA knowledge

- Experience with PMA supplements

- 510(k)

- 30 day manufacturing change notices.

Position just opened up, looking to fill immediately!


Visit Our Website

 
 


* 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.