Medpoint, LLC is conducting a search for Senior and Junior-level Regulatory Specialists at three different Client locations. Senior-level candidates must have a minimum of 10 years experience writing and submitting 510(k)
and Junior-Level candidates must have a minimum of 4 years experience assisting with writing and submitting 510(k). EU Regulation and PMA experience is preferred for both Senior and Junior-Level Regulatory Specialists.
Locations:
West Chester, Pennsylvania
Warsaw, Indiana
Raynham, Masschusetts
Travel: must be flexible to work both on and off-site
Duration: 1-2 years beginning immediately
Rate: Based on experience
Please send your CV and summary of 510(k) experience to [email protected].