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Stelle verifiziert vor 4 Stunden

Regulatory Expert (f/m/x)

EBG MedAustron GmbH·Wiener Neustadt (Niederösterreich)Vor Ort
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Vox-Zusammenfassung
  • Aufgaben: Verantwortung für regulatorische Aktivitäten bei der Entwicklung medizinischer Geräte, Koordination von Usability- und Risikomanagementaktivitäten, Erstellung technischer Dokumentation.
  • Anforderungen: Abgeschlossenes technisches oder naturwissenschaftliches Studium, Erfahrung mit ISO 13485, IEC 62304, gute Deutsch- und Englischkenntnisse.
  • Bedingungen/Vorteile: Mindestbruttogehalt nach Kollektivvertrag, mit Überzahlung möglich, unbefristete Vollzeitstelle, Standort in Wiener Neustadt.
An der Quelle bewerbenSie verlassen VoxJobs zu karriere.at — die Bewerbung erfolgt direkt beim Unternehmen. karriere.at

Stellenbeschreibung

Who we are: MedAustron International GmbH is a subsidiary of EBG MedAustron GmbH and realizes international technology projects in the course of the construction of a new particle accelerator in the rapidly growing medical technology sector. The parent company EBG MedAustron operates one of the most modern centers for ion therapy and research in Europe. As a Regulatory Expert, you will be responsible for regulatory activites for medical device development. You will work in a meaningful environment where your expertise will directly contribute to the successful development of innovative medical device projects and help advance technologies that ultimately benefit patients. Share our spirit and become part of our team as a Regulatory Expert (f/m/x) A job where you can make a difference: • Contribution to the compliant execution of regulatory activities for medical device development • Coordination and execution of usability engineering activities according to IEC 62366 • Contribution to risk management activities according to ISO 14971 • Definition of workflows and processes, especially regarding design control • Preparation of technical documentation • Implementation of regulatory strategies to obtain medical device approvals (MDR CE marking, FDA 510(k)), as well as participation in internal and external audits Skills that make you our strength: • Completed technical or scientific degree, e.g., in Medical Engineering, Mechanical Engineering, Electrical Engineering, Physics, or a comparable field • Strong understanding of product development processes and regulatory requirements in medical device development • Experience with medical device development according to ISO 13485 and with the medical software life cycle according to IEC 62304 is an advantage • Excellent organizational skills and a structured, solution-oriented working style • Strong communication skills and team-oriented mindset • Very good German and English language skills, both written and spoken For the advertised position we offer a minimum gross annual salary based on the classification in use group IV of the collective agreement for white-collar workers in the metal industry, with the possibility of a significant overpayment, depending on professional qualifications and experience. Further information on MedAustron International GmbH, our benefits and what matters to us can be found here. Ready to grow with us as a Regulatory Expert? Take the next step in your career and send us your application documents using our online application tool. Apply now

Transparenz-Panel

Originalquelle
karriere.at
Veröffentlicht
14. Juli 2026 · echtes Datum
Zuletzt verifiziert
vor 4 Stunden
Qualitäts-Score
35/100
Gehalt angegeben0
Unternehmen identifiziert0
applyUrl0
postedAt15
Vollständige Beschreibung20

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