Regulatory Affairs Specialist

vor 3 Wochen

Rohrdorf, Deutschland Medi-Globe Group Vollzeit

About Medi-Globe Group

We are a leading medical technology company specializing in urology and gastroenterology.

Our Team

We are seeking a highly skilled Regulatory Affairs Specialist to join our team in a dynamic and innovative environment.

Key Responsibilities:

  • Conduct product registrations in the EU and worldwide, ensuring compliance with regulatory requirements.
  • Collaborate with internal departments to ensure seamless product approvals and launches.
  • Coordinate with authorities to obtain necessary approvals and licenses.
  • Interpret and implement regulations, ensuring our products meet the highest standards.
  • Approve documents in our management system, maintaining accurate and up-to-date records.

Requirements:

  • Minimum of 3 years of experience in Quality Management or Regulatory Affairs.
  • Experience in international registration processes, with a strong understanding of regulatory frameworks.
  • Proficiency in English, with excellent communication and team skills.

What We Offer:

  • A permanent full-time contract with opportunities for growth and development.
  • Diverse and challenging tasks, with a focus on innovation and excellence.
  • Benefits such as company events, health promotion, and a home-office option.

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