Familial and
international in one.
Celine Villiger
Exciting challenges await on the path to realizing our vision. We are therefore seeking

Regulatory Affairs Manager

Root
Your tasks Your qualifications

• C ompilation of complete Technical Documentations of > 3 years experience in Regulatory Affairs in medical device
  class III products compliant to MDR requirements
  industry


• Prepare submission dossiers compliant with national > Experience in collaborating with Notified Bodys and/or
  regulations as needed Health Authorities


• C oordinate submission timelines with other departments, > Collaborative, independent working style and good
  Notified Bodys/Health Authorities and business partners
  communication skills


• C ritical review of reports and plans as part of these > Bachelor or Master degree in natural science
  submissions


• Excellent English and good German skills


• Writing of submission summarys

Geistlich Pharma is a family-run Swiss company and a longstanding global leader in regenerative dentistry. We have a long tradi-
tion of pioneering attitudes that place the focus on employees. These employees are dedicated to the spirit that drives our company
to excel: a passion for regeneration. This is the origin of our innovative medical products that reconstruct bones, cartilage and soft
tissue. Our motivated team looks forward to working with you in a modern, dynamic environment with international flair.
We look forward to receiving your completed electronic application at: recruiting@geistlich.ch
If you have any questions about the position, please contact: Marco Steiner, Deputy Director & Group Lead Regulatory Affairs,

• 41 41 492 55 55

www.geistlich-pharma.com