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  • Hamburg, Hamburg, Deutschland apoqlar Vollzeit

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  • Hamburg, Hamburg, Deutschland apoqlar Vollzeit

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  • Hamburg, Hamburg, Deutschland apoqlar Vollzeit

    About the RoleWe are seeking a highly skilled Regulatory Affairs and Quality Management Lead to join our team at apoQlar. As a key member of our Regulatory & Quality Management team, you will play a leading role in ensuring our medical mixed reality platform is in compliance with regulatory and statutory requirements.Key ResponsibilitiesDevelop and lead the...

Werkstudent Quality and Regulatory Affairs

vor 5 Monaten


Hamburg, Deutschland D.Med Consulting GmbH Vollzeit

Die D.Med Consulting GmbH ist ein Zusammenschluss der Fresenius Medical Care AG & Co. KGaA (51%) und der D.Med Healthcare Gruppe (49%), einem weltweit operierenden Anbieter von medizinischen Dienstleistungen und Medizinprodukten im Bereich Nephrologie, Kardiologie und der Inneren Medizin. Gegründet 2011 und mit Hauptsitz in Hamburg steht die D.Med Consulting GmbH für erstklassige Forschungs
- und Entwicklungs
- sowie Beratungsdienstleistungen mit Schwerpunkt Extrakorporale Therapien.

Wir suchen ab sofort Nachwuchstalente der naturwissenschaftlichen und technischen Studienrichtungen, gerne mit Vertiefung in Medizintechnik, Mechanik, Prozess
- und Regelungstechnik oder praktischer Informatik, die bei uns ihre Karriere mit einer Werkstudententätigkeit beginnen möchten. Verstärken Sie unser Team am Standort Hamburg als
**Werkstudent Quality and Regulatory Affairs (m/w/d)**:
**Ihre Aufgaben**
- Beteiligung beim Qualitätsmanagement und regulatorischen Themen rund um die Entwicklung von innovativen Produkten der Medizintechnik
- Unterstützung bei der Ermittlung und GAP-Analyse von regulatorischen Anforderungen für verschiedene aktive und nicht aktive Medizinprodukte
- Unterstützung bei der Aufrechterhaltung und Verbesserung eines Qualitätsmanagementsystems nach EN ISO 13485
- Projektmanagement Support für die Entwicklung eines aktiven Medizinprodukts
- Unterstützung bei der Erstellung und Aktualisierung von Technischer Dokumentation

**Ihr Profil**
- Naturwissenschaftliches oder technisches Studium, gerne mit Vertiefung in Medizintechnik, Qualitätsmanagement oder Regulatory Affairs
- Erste praktische Erfahrung durch Praktika oder Werkstudententätigkeiten, gerne im Bereich Medizintechnik, Qualitätsmanagement oder Regulatory Affairs
- Leidenschaft für Ihre Aufgaben sowie Organisationsfreude
- Selbständige und zuverlässige Arbeitsweise
- Aufgeschlossene Persönlichkeit, Kommunikationsstärke, Motivation und Teamfähigkeit
- Versierter Umgang mit MS Office
- Sehr gute Englischkenntnisse in Wort und Schrift

**Wir bieten**
- Den Anforderungen entsprechende Vergütung
- Interessantes, abwechslungsreiches Aufgabengebiet
- Einen modernen Arbeitsplatz im Herzen Hamburgs bei einem internationalen und zukunftsträchtigen Arbeitgeber
- Übernahmemöglichkeit nach Abschluss Ihres Studiums
- Dynamisches und motiviertes Team
- Flexible Arbeitszeiten sowie anteiliger Urlaubsanspruch
- Persönliche Mehrwerte wie z.B. betriebliche Altersvorsorge, Mitarbeiterevents, Zugang zur Plattform corporate benefits u.v.m.

**D.Med Consulting GmbH** | Bernhard-Nocht-Str. 99 | 20359 Hamburg, Deutschland | Tel: +49 211 650 415 13