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Regulatory Affairs Expert (all genders)

Regulatory Affairs Expert (all genders)

Regulatory Affairs Expert (all genders)

Regulatory Affairs Expert (all genders)

Merck

Pharmazeutische Produkte, Arzneimittel

Darmstadt

  • Art der Beschäftigung: Vollzeit
  • 63.000 € – 87.000 € (von XING geschätzt)
  • Vor Ort
  • Zu den Ersten gehören

Regulatory Affairs Expert (all genders)

Über diesen Job

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.

Your Role: We are seeking a motivated and skilled regulatory partner, specialized in electrical and electronic equipment (EEE), to join our regulatory business transformation team. This role will support our activities in the Life Sciences field by defining and executing regulatory and compliance strategies for the life cycle management of our EEE product portfolio. You will act as a subject matter expert for EEE topics, ensuring compliance with global regulatory requirements while collaborating closely with internal and external stakeholders. In this position, you will advise partners on global regulatory requirements related to EEE, including safety, electromagnetic compatibility (EMC), RoHS, WEEE, REACH, and other applicable standards. You will define and implement regulatory and compliance strategies for EEE products, ensuring alignment with company objectives. Managing stakeholder communication is a key aspect of your role, as you will foster strong relationships with internal teams and external partners to facilitate clear understanding of regulatory requirements. You will oversee the flow of information throughout the value chain, ensuring that all regulatory aspects are integrated into project plans. Your focus on change management practices will support successful implementation of regulatory strategies and initiatives. You will assess risks related to regulatory compliance and develop strategies to mitigate identified risks, while effectively managing resources to ensure timely achievement of key project deliverables and objectives.

Who You Are:

  • Higher education (university and/or engineering degree) in environmental sciences or regulatory affairs
  • 5 years+ of experience in regulatory compliance, particularly concerning EEE
  • Strong understanding of global regulatory frameworks and standards for EEE
  • Excellent analytical and problem-solving skills related to regulatory risks
  • Strong communication and interpersonal skills, with the ability to work collaboratively in a cross-functional environment
  • Proven ability to manage multiple projects and meet deadlines
  • Experience in a multinational company or in a regulatory role in the EEE sector
  • Knowledge of product lifecycle management and regulatory submission processes
  • Certification in regulatory affairs (e.g., RAC) is an asset
  • Fluent English is essential

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!

Gehalts-Prognose

Unternehmens-Details

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Merck

Pharmazeutische Produkte, Arzneimittel

10.001 oder mehr Mitarbeitende

Darmstadt, Deutschland

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