Description
Do you have experience with a PMA submission? What about five years of regulatory affairs experience? Are you a hands-on leader? Do you possibly have a scientific degree? If you answered yes to these questions, and also are hungry to work on complex technology that will change the medical device industry, then I would love to hear from you.As regulatory affairs manager for this company that has less than 150 people, you will play an avid role in the PMA submission. You will help develop the regulatory team and build it for the future by coordinating with the FDA and other international agencies, and you will help represent the regulatory team in inter-departmental matters. You will also mentor the younger regulatory staff as well as hire new regulatory employees. This may likely be the most complex technology you have ever worked on, and it is a chance to jumpstart the treatment of a disease that harms millions of Americans every year. I look forward to hearing from you.
To find out more about Real please visit www.realstaffing.com