Regulatory Affairs Manager (m / f / d)

Lohmann & Rauscher GmbH & Co. KG; Neuwied; Vor Ort; EUR 50.000 - 80.000; Vollzeit

Zusammenfassung

A leading global supplier of medical devices seeks a Regulatory Affairs Manager to oversee international product registrations, particularly in Latin America. This role requires a strong background in regulatory affairs, project management, and proficiency in English and German. The company values work-life balance and offers professional development opportunities through its L&R Academy.

Leistungen

Professional development opportunities

Flexible work-life balance solutions

Qualifikationen

• Experience in international registration of medical devices.
• Very good command of English and German; knowledge of Spanish and Portuguese is a plus.

Aufgaben

• Manage international registration of products in Latin America.
• Coordinate and implement regulatory projects efficiently.
• Monitor changes in regulatory requirements for Latin America.

Kenntnisse

Regulatory knowledge

Project management

Analytical skills

Monitoring skills

Communication

Ausbildung

University degree or diploma in natural sciences

Tools

MS Office

Jobbeschreibung

A team of more than 5,500 co-workers around the globe.

A company with a stance, a vision, and the values of a family-run enterprise.

A modern and forward-looking corporate culture.

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.

Take your chance. We would like to have you in our team as

Regulatory Affairs Manager (m / f / d)

Location: Neuwied

• When it comes to regulatory affairs, your knowledge of laws and regulations is as vast as it is invaluable. Perfect! As our Regulatory Affairs Manager, your main responsibility lies in the international registration 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 run smoothly.
• Whether it comes to the coordination, planning, implementation, or testing of relevant documentation, your performance consistently proves to be efficient and high-quality.
• Requirements include a 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; knowledge of other languages, especially Spanish and Portuguese, is a plus.
• You want to participate 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 through our L&R Academy.