WI-Madison, Summary: The QTI Group has partnered with a leading pharmaceutical company to recruit for an Regulatory Affairs Specialist to join their Quality team. This individual will help prepare and maintain regulatory agency submissions and maintain required compliance reports, such as Drug Master Files (DMFs) and related updates and amendments, to comply with US FDA and European Community (EC) requirement
Job Online on Website: http://jobview.monster.com/Regulatory-Affairs-Specialist-Job-Madison-WI-US-192798554.aspx
