(Senior) Manager Drug Regulatory Affairs (m/f/d)

JR Germany; Frankfurt; Vor Ort; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

Join a forward-thinking company as a (Senior) Manager in Drug Regulatory Affairs, where you'll play a crucial role in facilitating pharmaceutical marketing authorizations across Europe. This position requires a detail-oriented professional with a strong background in regulatory affairs and a passion for healthcare innovation. You will collaborate with diverse teams, ensuring compliance and strategic planning while maintaining relationships with regulatory authorities. If you're ready to make a significant impact in the healthcare sector, this opportunity is perfect for you.

Qualifikationen

• At least 3 years of experience in drug regulatory affairs.
• High level of precision and strategic thinking required.

Aufgaben

• Provide regulatory support for pharmaceutical marketing authorizations.
• Coordinate European procedures and maintain relationships with authorities.

Kenntnisse

Regulatory Affairs

Strategic Planning

Communication Skills

Problem Solving

Detail-oriented

IT Skills

Team Player

Ausbildung

University Degree in Sciences

Tools

Regulatory IT Tools

Jobbeschreibung

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(Senior) Manager Drug Regulatory Affairs (m/f/d), Frankfurt am Main

Job Details

• Client: [Client information not provided]
• Location: Frankfurt am Main
• Job Category: Other
• EU work permit required: Yes
• Job Views: 2
• Posted: 28.04.2025
• Expiry Date: 12.06.2025

Job Description

We are committed to providing the best solutions to medical professionals, enabling them to address their challenges effectively. Fresenius Kabi is a leader in healthcare innovation. We value diversity and different backgrounds.

• Regulatory support for international pharmaceutical marketing authorizations
• Planning, implementation, and coordination of European procedures (MRP/DCP)
• Strategic planning and implementation of variations both within and outside Europe
• Establishing and maintaining relationships with regulatory authorities and third parties
• Supporting local market units with regulatory tasks
• Participating in projects by providing regulatory expertise
• Monitoring the regulatory environment and assessing its relevance to the product portfolio

Qualifications

• Completed university degree in sciences
• At least 3 years of experience in European and international drug regulatory affairs
• Structured working style, detail-oriented, team player, problem solver
• High level of precision and strategic thinking
• Excellent communication skills
• Proficiency in English (written and spoken)
• Good IT skills and interest in regulatory IT topics