Emergo Group, Inc. is an ISO 9001:2008 registered consulting firm that serves the medical device sector. We ensure our clients' compliance by offering comprehensive, customized Quality Assurance and Regulatory Affairs solutions. The majority of our client base is comprised of small to medium-sized Medical Device manufacturers that are required to develop, implement and/or maintain ISO Quality Assurance Systems in order to export their products. We have offices in Austin, Texas, The Netherlands, France, Germany, UK, Australia, Canada, China, Japan, Russia, Mexico, and Brazil.
In the US and Europe we are seeking to fill positions for Regulatory Consultants who have at least 10 years of experience in a variety of therapeutic areas with technical file and design dossier compilations and FDA submissions, in particular 510(k)s and pre-IDEs. Ideally also experience with IVDs, active devices and devices containing software.
Please send your resume to careers [at] emergogroup [dot] com and let us know if you are interested in a full time position or working with us on a contract basis.