GMED North America is seeking a Lead Auditor for medical devices to conduct ISO 13485/MDSAP audits and CE marking activities. This is a home-based role with travel to client sites, reporting to the Unit Manager.
The ideal candidate has hands-on technical experience in active and non-active devices, plastics and metals, with at least four years in R&D, manufacturing, testing or auditing of medical devices and two years in quality management. Remote work is possible.
#J-18808-LjbffrRemote Medical Device QA Lead Auditor in workfromhome at Unknown Company
This position is listed as full time and able to be worked remotely.