support registration activities. Requirements Have a minimum 3 years of professional experience in regulatory affairs, preferably in medical device industry Have technical writing skills Understand
support registration activities. Requirements Have a minimum 3 years of professional experience in regulatory affairs, preferably in medical device industryHave technical writing skillsUnderstand technical
Inhouse Kurse: z. B. TEE, ALS, AFS Weitere spezielle Karrieremöglichkeiten: Clinician Scientist Programme, Master of Medical Education, Master of Business and AdministrationAngebote zur Vereinbarkeit