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Regulatory Affairs Manager

Geistlich Pharma AG

vor 3 Wochen

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Exciting challenges await on the path to realizing our vision. We are therefore seeking

Regulatory Affairs Manager

Your tasks
  • Compilation of complete Technical Documentations of class III products compliant to MDR requirements
  • Prepare submission dossiers compliant with national regulations as needed
  • Coordinate submission timelines with other departments, Notified Bodys/Health Authorities and business partners
  • Critical review of reports and plans as part of these submissions
  • Writing of submission summarys
Your qualifications
  • 3–5 years experience in Regulatory Affairs in medical device industry
  • Substantial experience in collaborating with Notified Bodys and/or Health Authorities
  • Collaborative, independent working style and good communication skills
  • Master degree or PhD in natural science or medicine
  • Excellent English and good German skills

Our motivated team looks forward to working with you in a modern, dynamic environment with international flair.

If you have any questions about the position, please contact: Marco Steiner, Deputy Director & Group Lead Regulatory Affairs, +41 41 492 55 55

Geistlich Pharma AG
D4 Business Village
Platz 10
6039 Root D4
041 492 55 55