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Head Regulatory Affairs Medical Technology (m/w)

Stettler Consulting AG

Employment type
Full-time
Workload
100%
Location
St. Gallen
Company
Stettler Consulting AG, 9000 St. Gallen
First posted
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Top products & intelligent digital solutions.

Are you a person who enjoys seeking solutions to create a good framework for product novelties and approvals? Then there is a leading Swiss medical technology company in the Eastern Switzerland region that definitely wants to get to know you. The globally active manufacturer sells technically high-quality devices and instruments for surgery. The company combines the values of quality, continuity and reliability with dynamism, pioneering spirit and innovation. Region: Eastern Switzerland.

What you can look forward to:

  • Exciting, varied activities with freedom for ideas and initiative
  • Successful Swiss SME in an international environment and in the innovative healthcare industry
  • Attractive and flexible working and employment conditions

Your area of responsibility and tasks:

  • Disciplinary and technical leadership as well as support of the RA employees
  • Planning, coordination and completion of regulatory activities (MDR 2017/745 and other standards) and international approval procedures for active and non-active medical devices in Switzerland, Europe, USA, CSA and Asia
  • Collaboration with the development department
  • Creation of technical documentation for medical devices as well as adaptation of existing documentation
  • Support of quality management initiatives and usability studies as well as participation in change management
  • Technical leadership in interdisciplinary project teams for product approval as a representative of the Regulatory Affairs department
  • Maintenance and review of technical product files regarding legal requirements

Your profile:

  • Successfully completed higher technical or scientific education at FH or Uni level
  • Professional and initial leadership experience in medical technology and in the field of Regulatory Affairs
  • Experience in the creation of technical documentation and in the creation of approval documents
  • Current knowledge of the normative and regulatory requirements for medical devices
  • Very good German and English skills

Contact

Call us or send your application documents stating the reference number JB-211.
Roger Stettler and Anja Weisflog look forward to meeting you personally.

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Posted 2 days ago

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