Regulatory Affairs Specialist
- Maastricht
As Regulatory Affairs Specialist and member of the quality assurance and regulatory affairs team you play a key role in processes that ensure patients safety and regulatory compliance of all Technomed medical devices. Trefwoorden: Regulatory Affairs Specialist, Regulatory Affairs Manager, Regulatory Affairs, Regulatory Affairs Officer, Biomedical Engineering, Validation Engineer, Verification Officer, Quality Engineer, ISO 13485, Medical Devices Directive (MDD), Medical Devices Regulation (MDR), FDA, Regulations, RA, RA medewerker, Clinical Research, Biomedical, Medical Devices, Government
As Regulatory Affairs Specialist and member of the quality assurance and regulatory affairs team you play a key role in processes that ensure patients safety and regulatory compliance of all Technomed medical devices. Trefwoorden: Regulatory Affairs Specialist, Regulatory Affairs Manager, Regulatory Affairs, Regulatory Affairs Officer, Biomedical Engineering, Validation Engineer, Verification Officer, Quality Engineer, ISO 13485, Medical Devices Directive (MDD), Medical Devices Regulation (MDR), FDA, Regulations, RA, RA medewerker, Clinical Research, Biomedical, Medical Devices, Government
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