Medical Device Regulatory Affairs

Carlsbad, CA

Job ID: 127455 Industry: CLINICAL

 

Medical Device Regulatory Affairs

Project Description:                                                     

Our client is currently in need of a regulatory affairs consultant to come on site and help with a multitude of projects.  The projects will include a series of international registrations along with labeling projects.  The purpose of this project is to effectively complete the integration of two different companies and sites.

 

Day to Day Responsibilities:

This consultant will be coming on site and help drive the submission and tech file update process for the client.  The person chosen for this role will support the transition of registrations and label changes for the transfer.  The consultant will also be responsible for informing the client of regulatory requirements and emerging issues which may affect the registration approval process.  This role also entails the review and approval of labeling materials. 

Required Skills:

Regulatory Affairs

Registrations

Submissions

Labeling

Job Type: Contract

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