Medical Device Regulatory Affairs procedure writing


Job ID: 125852 Industry: CLINICAL


Medical Device Regulatory Affairs procedure writing

Project Description:                                                     

Our client is currently in need of a consultant to come on board and help consolidate their procedures.  Right now, their regulatory procedure documents are not harmonized and need to be consolidated.  The client would like this consultant to have an understanding of the process of submissions, global registrations, license registrations, regulatory tracking, data collection, etc.  


Day to Day Responsibilities:

This consultant will be responsible for gathering the information on how the client would like to proceed in certain regulatory areas.  This consultant will then take the information and harmonize the procedures by putting the process into terms that can be easily understood.  These procedures will be related to regulatory projects such as submissions, global registrations, license registration, tracking, data collection, and other regulatory practices.  The client is a medical device organization, therefore expertise in medical device is a must.  

Required Skills:

Procedure Writing

Medical Devices

Regulatory Affairs

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