Medical Director

vor 4 Wochen


Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit
Join Our Team as a Manager Regulatory Affairs Clinical

We are seeking a highly skilled and experienced Manager Regulatory Affairs Clinical to join our global team at PAUL HARTMANN AG. As a key member of our regulatory affairs team, you will play a critical role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements.

Key Responsibilities:
  • Coordinate external service providers to support clinical evaluation documentation, PMCF, and PMS
  • Support risk analysis and study planning for CE and PMCF studies
  • Develop and implement regulatory strategies to ensure compliance with relevant regulations and guidelines
  • Collaborate with cross-functional teams to ensure effective communication and coordination
Requirements:
  • Professional experience in the medical device environment or another regulatory field of work
  • Experience in literature search and review, as well as knowledge of regulatory medical writing
  • Knowledge of database management and IT affinity
  • Fluent written and spoken English
What We Offer:
  • International mobile working
  • Attractive ways of combining work and family life, e.g. childcare subsidy
  • 30 days paid leave per year, plus special leave for exceptional life events
  • Company pension plan with attractive employer contribution
  • Various health and fitness offers, e.g. skin cancer screenings, online courses for mental health

Apply now via our online platform to take the first step in your career as a Manager Regulatory Affairs Clinical at PAUL HARTMANN AG.



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