EU Regulatory Lead

vor 1 Woche

Frankfurt am Main, Hessen, Deutschland Merck KGaA Vollzeit

Work Your Magic with us

Ready to explore, break barriers, and discover more? We know you've got big plans – so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your role

The EU Regulatory Lead (EU RL) is responsible for the regulatory strategy and execution for their assigned projects in their EU region and respective countries. The EURL represent and provide input for the respective EU region at the GRST. The person may provide direct input to the GPT in case of major region, particularly where the GRL is not in that region. The person lead the respective regional regulatory sub-team and drive the regulatory submission in the EU region. The person ensure optimal planning in alignment with cross-functional team, and execution to plan for both development submissions and maintenance submissions to ensure ongoing compliance. Partnering with Regulatory Project Management and Submission Management is a key stakeholder management. The person participate in cross-functional and GRA initiatives.

Who you are

  • Considerable Regulatory Affairs experience
  • Advanced scientific degree or equivalent
  • Minimum 3 years of experience in drug development, preferably in Regulatory Affairs
  • Skilled in matrix leadership
  • Influencing and interpersonal communication skills
  • Excellent spoken and written English

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity

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