Progressive

Regulatory Affairs Manager EU

Stellenbeschreibung:

The following responsibilities are awaiting you:

  • You prepare and submit applications for conformity assessments and clinical trials involving non-active implantable class III medical devices in the EU.
  • You coordinate timely and accurate responses to questions from Notified Bodies and Competent Authorities.
  • You compile, assess and update CE technical documentation and clinical trial application dossiers, including documentation provided by third parties.
  • You advise cross-functional development teams on quality, analytical, preclinical, and clinical requirements to support the acceptance of regulatory submissions.
  • You prepare and maintain product information in accordance with company core data, applicable legislation, and relevant guidelines.
  • You manage the regulatory life cycle of CE-marked products, including renewals, change notifications, and annual updates.
  • You assess regulatory implications of changes proposed by production sites, marketing teams, and other internal stakeholders.
  • You coordinate regulatory projects and collaborate with external partners, including consultants, contract research organizations, and distribution partners.
  • You develop regulatory strategies, contribute to cross-functional project teams, and serve as a contact person for regulatory requirements.
  • You identify country-specific requirements and manage the submission and maintenance of documentation required in EU countries beyond the CE mark.
  • You support additional regulatory activities and responsibilities as required.

What we expect from you:

  • You hold a degree in natural sciences, pharmacy, biology, chemistry, engineering (medical devices / bioengineering), or a comparable discipline, ideally at master's or PhD level.
  • You bring approximately 1-3 years of professional experience in EU regulatory affairs for medical devices.
  • You have a sound understanding of the European regulatory landscape for medical devices.
  • You demonstrate strong time management, problem-solving, communication, and digital skills.
  • You work independently, remain resilient, and approach challenges with a structured and solution-oriented mindset.
  • You collaborate effectively across functions and are able to coordinate projects and influence stakeholders without direct authority.
  • You build constructive relationships with internal and external partners, including Notified Bodies and Competent Authorities.
  • You communicate fluently and confidently in business English.
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EnglishEN: Please refer to Fuchsjobs for the source of your application
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Stelleninformationen

  • Veröffentlichungsdatum:

    01 Okt 2026
  • Standort:

    Frankfurt

    Einsatzort:

    Germany
  • Typ:

    Vollzeit
  • Arbeitsmodell:

    Vor Ort
  • Kategorie:

  • Erfahrung:

    2+ years
  • Arbeitsverhältnis:

    Angestellt

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