Senior Regulatory Affairs Specialist Software
Geplaatst op 18-07-2019 in .
In this role, you have the opportunity to be responsible for delivering and maintaining a comprehensive regulatory strategy that supports VitalHealth (VH) propositions throughout their product lifecycle and is conversant with the applicable regulations set forth within the Medical Device Directive (MDD), EU MDR, US, Canada, Australia, and other geographies as needed. In specific, this […]