Regulatory Affairs Manager

vor 2 Monaten

Zug, Zug, Schweiz KMP MANAGEMENT CONSULTING Vollzeit
Aufgaben und Verantwortlichkeiten

Als Regulatory Affairs Manager sind Sie für die Einhaltung der regulatorischen Anforderungen für Medizinprodukte verantwortlich. Sie müssen sicherstellen, dass Produkte und Prozesse den neuen und existierenden regulatorischen Anforderungen entsprechen.

Qualifikationen und Erfahrungen
  • Erfolgreich abgeschlossenes Studium im wissenschaftlichen, medizinischen oder technischen Bereich oder vergleichbare Ausbildung
  • Mehrjährige Berufserfahrung als Spezialist im Regulatory Affairs und/oder Qualitätsmanagement vorzugsweise in branchennahen Unternehmen mit internationaler Ausrichtung
  • Sehr gute Kenntnisse der Regularien für Medizinprodukte
  • Gute analytische Fähigkeiten
  • Sicher in der Umsetzung von Moderations- und Präsentationstechniken
  • Proaktives und lösungsorientiertes Vorgehen
  • Sehr gute Deutsch- und Englischkenntnisse, jede weitere Fremdsprache ist vom Vorteil
Vorteile
  • Eine interessante Aufgabe in einem innovativen, international tätigen Familienunternehmen
  • Eine Unternehmenskultur, in der es Spaß macht, Ideen, Kraft und Initiative einzubringen
  • Mitarbeit in einem engagierten Team
  • Flache Hierarchien und kurze Kommunikationswege
  • Überdurchschnittliche Sozialleistungen

Wir suchen nach einem motivierten und erfahrenen Regulatory Affairs Manager, der sich in unserer dynamischen und innovativen Umgebung wohlfühlt. Wenn Sie sich für diese Herausforderung interessieren, senden Sie bitte Ihre vollständigen Bewerbungsunterlagen einschließlich Ihres Fotos und Ihrer frühestmöglichen Eintrittstermins sowie Ihrer Gehaltsvorstellungen an den unten genannten Ansprechpartner.

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