Medical Device EU MDR Specialist

Princeton, NJ

Job ID: 131609 Industry: Regulatory & Scientific

Medical Device EU MDR Specialist

 

Background:

The client is a large medical device company who are preparing to start their EU MDR remediation project. They are budgeted and approved to bring on two EU MDR Specialists to update the technical files and design dossiers for their products in the EU. They want to bring on two Specialists with experience updating these types of documents. The consultants are expected to have an understanding of European medical device regulations.

Project:

The consultants will be EU MDR SMEs that will come onto the Regulatory team and work with the full-time employees to analyze and interpret all aspects of the new European regulations and how they relate to the devices of the client. They will be responsible for taking the pertinent information and updating the technical files and design dossiers accordingly. It is expected that these consultants will have the experience and capability to work autonomously to complete these updates.

Required:

EU MDR

Technical File Updates

Design Dossier Updates

 

Job Type: Contract

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