http://www.johnstonsearch.com/blog In this brief (1min) Video, Brian explains the “meat” his client (23 placements since 2004) needs for your dynamic Senior Regulatory Affairs Specialist role.
• You must have prepared FDA submission. (USA/International)
• Success with IDE’s in Class III Medical Device.
• Accomplished PMA submission/preparation from scratch
• BS, Biology, RA, etc.
Until you apply or refer your accomplished friend, enJOY your day!
Yours in Expert Medical Device Recruitment,