Morristown, NJ

Program Manager, Regulatory Affairs

The Program Manager, Regulatory Affairs is responsible for planning and timely submission of regulatory filings for new and existing marketing authorizations. 

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Morristown, NJ

Regulatory Affairs Associate

With supervision, helps to author, compile, review and submit high-quality regulatory submissions to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws. Under supervision, coordinates and writes clear, concise and accurate responses to inquiries from FDA resulting from their review of the submissions.  

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