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Regulatory Manager

Company: Midmark Corporation
Location: Dayton Ohio
Category: Manufacturing

Job Description:
This position assures company compliance to all pertinent United States F.D.A. state and international regulatory requirements which are applicable to the design manufacture and distribution of medical and diagnostic devices by performing the following duties:Responsibilities: Develops content and format for regulatory submissions. Coordinates submission of annual FDA registration updates to device listing MDRs 510(k)s and recall notices. Coordinates submission of documentation for international regulatory requirements including the European Medical Device Directive (See More)
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