Regulatory Affairs Manager (m/f/d)

JR Germany; Neuwied; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

Join a leading global medical device company as a Regulatory Affairs Manager in Neuwied. You will leverage your expertise in regulatory affairs to manage international product registrations, ensuring compliance and smooth operations in Latin America. The role offers career development opportunities and a supportive work-life balance.

Leistungen

Support for maintaining work-life balance

Individual career development through L&R Academy

Qualifikationen

• Experience in international registration of medical devices.
• Knowledge of laws and regulations in regulatory affairs.

Aufgaben

• Manage regulatory projects within product development.
• Monitor regulatory changes in Latin America.
• Coordinate and implement relevant documentation.

Kenntnisse

Regulatory Affairs

Fluency in English

Fluency in German

Knowledge of Regulatory Submissions

Ausbildung

University Degree in Natural Sciences

Tools

MS Office

Jobbeschreibung

Job Details

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Job Views:

2

Posted:

16.05.2025

Expiry Date:

30.06.2025

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Job Description:

Join a team of over 5,500 co-workers worldwide, within a company that values a family-like culture, vision, and modern corporate environment.

We are seeking top talents to bring their expertise, ideas, and aspirations to our international teams. L&R is a global leader in medical device development and manufacturing, offering innovative, customized solutions for patient care and healthcare professionals, including advanced wound dressings and high-tech therapies like negative-pressure wound therapy.

Take your career to the next level by joining us as:

Regulatory Affairs Manager (m/f/d)
Location: Neuwied

• Are you knowledgeable about laws and regulations in regulatory affairs? Your expertise will be crucial as our Regulatory Affairs Manager, focusing on international registrations of our products in Latin America.
• You will manage regulatory projects within product development, employing a structured, analytical, and proactive approach.
• You will monitor regulatory changes in Latin America to ensure our product registrations proceed smoothly.
• You will coordinate, plan, implement, and test relevant documentation efficiently and with high quality.
• Requirements include a university degree in natural sciences, experience in international registration of medical devices, knowledge of regulatory submissions and MS Office, and fluency in English and German. Additional languages like Spanish and Portuguese are advantageous.
• We offer opportunities to participate in developing future medical devices, support for maintaining work-life balance, and individual career development through our L&R Academy.