Regulatory affairs specialist
Budapest
MEDITECH KFT
… CE marking activities (per MDD and EU MDR), including preparation and maintenance … surveillance activities, ensuring compliance with MDR and other regulatory requirements;Participate … 820, 803, 806, and 830, MDSAP, MDR, ISO 13485, etc.);Product registration …
profession.hu - 6 napja - szponzorált - Mentés