Our client:

A dynamic and internationally successful medical device companyin the Kanton of Graubünden, Switzerland.

Job description:

• Interaction with regulatory agencies and partners regarding vigilance cases and ensuring their questions are addressed within established time-frames
• Compilation of investigation details to support global vigilance reporting requirements
• Responsibility for vigilance reports and ensure reports are submitted to regulatory agencies or partners within required timelines
• Definition of safety measures (FSCA), active participation in product recalls and recall communications to markets and health authorities as required
• Keeping up to date with regulatory and normative requirements and ensuring their implementation in day-to-day business

The ideal candidate:

• Technical degree or comparable qualification
• Minimum 3 years professional experience in the Medical Device Industry; preferably in Post-Market Surveillance.
• Practical knowledge in relevant regulations such as 21 CFR 820, MDR, MDD, and ISO 13485 / IEC 60601
• Results oriented, multi-tasker, and quick learner; demonstrated ability to respond to the urgent needs of the team and track record of meeting agreed upon deadlines
• Fluency in English and German language

The process:

• CV an: m.burgstaller@sciproglobal.de
• Phone call and discussion of the job opportunity.
• Guidance through whole interview process and possible discussion of other opportunities.

Mein Kontakt.

• E-Mail: m.burgstaller@sciproglobal.de
• Tel: +41 43 508 92 17
• Xing: https://www.xing.com/profile/Michael_Burgstaller19/cv