Regulatory Affairs Manager (m/w/d)

UniNow GmbH; Neuwied; Vor Ort; EUR 60.000 - 90.000; Vollzeit

Zusammenfassung

Ein global aktives Unternehmen im Bereich der medizinischen Geräte sucht einen Regulatory Affairs Manager für Unterstützung bei internationalen Produktregistrierungen, besonders in Lateinamerika. Das Unternehmen bietet individuelle berufliche Weiterentwicklung, eine ausgewogene Work-Life-Balance und die Möglichkeit zur Mitgestaltung zukünftiger medizinischer Geräte.

Leistungen

Berufliche Weiterbildung

Individuelle Entwicklungsmöglichkeiten

Flexible Arbeitszeiten

Qualifikationen

• Berufserfahrung in der internationalen Registrierung von medizinischen Geräten.
• Sehr gute Englisch- und Deutschkenntnisse, andere Sprachen sind von Vorteil.

Aufgaben

• Verantwortlich für internationale Produktregistrierungen in Lateinamerika.
• Management von regulatorischen Projekten in der Produktentwicklung.
• Koordination und Umsetzung relevanter Dokumentationen.

Kenntnisse

Kenntnisse der regulatorischen Einreichungen

Analytische Fähigkeiten

Proaktive Arbeitsweise

Überwachung regulativer Anforderungen

MS Office Kenntnisse

Englischkenntnisse

Deutschkenntnisse

Spanischkenntnisse

Portugiesischkenntnisse

Ausbildung

Universitätsabschluss oder Diplom in Naturwissenschaften

Jobbeschreibung

Einleitung

We're looking for top talents who wish to introduce their know-how, ideas, and aspirations into our international teams. L&R is a globally active and expanding
supplier of medical devices. Our core business is the development and manufacture of innovative, customised solutions for the problems faced by patients
and healthcare professionals around the world: from modern wound dressing material to high-tech solutions like negative-pressure wound therapy.

Lohmann & Rauscher
Pharma & Gesundheit

Regulatory Affairs Manager (m/w/d)

Festanstellung, Qualität
Neuwied

How you can help us

When it comes to regulatory affairs, your knowledge on laws and regulations is as vast as it is invaluable? Perfect! As our Regulatory Affairs Manager your main responsibility lies on international registrations of our products in Latin America.
Within the context of product development, you successfully manage regulatory projects. Your mindset? Structured and analytical. Your approach? Hands-on and proactive.
As an expert in your field, you keep a keen eye on any changes regarding regulatory requirements for Latin America. Thanks to you and your monitoring skills, our international product registrations go like clockwork.
Whether it comes to the coordination, planning, implementation or testing of relevant documentations, your performance continuously proves to be efficient and high-quality.

What you have to offer

University degree or diploma in natural sciences
Work experience in the international registration of medical devices
Working knowledge of regulatory submissions and MS Office
Very good command of English and German, other languages (especially Spanish, Portuguese) are a plus

Why you decide to join L&R

You want to take part in developing future medical devices. We offer you the chance to do so.
Your work-life balance is important to you. We will find a solution that fits your needs.
Professional development is on your agenda. We will advance your career individually at our L&R Academy

We would like to meet you! Please send us your application incl. your salary expectation via our Career Center.

Your contact: Silke Krumbholz (Tel: [phone])