Regulatory Affairs Freelance in Medtech (3- to 6-month assignment) (F/M)

Decomplix is a compliance partner that simplifies market access for medical devices. As a Swiss Authorized Representative (SAR), Decomplix goes beyond just consulting. Quality management and regulatory affairs are our core competence. In support of our core team, we are looking for a Regulatory Affairs Freelance in Medtech (3- to 6-month assignment) (F/M)

You take on

  • contribution to the Swiss Authorized Representative (SAR) services we provide to foreign medical device manufacturers, depending on your strengths and interests;
  • regulatory support to internal initiatives to improve our services;
  • regulatory monitoring of the applicable legislation in Switzerland.

You bring

  • a scientific or technical background;
  • an initial regulatory affairs experience in the Medtech industry;
  • the ability to quickly grasp, generalize and synthesize complex technical concepts, and make them easily understandable in text and pictures;
  • attention to detail and customer focus;
  • good knowledge of German and English, spoken and written.

You want

  • to expand your regulatory affairs competence, by working with various companies and products;
  • to work independently, entrepreneurially and also take on new tasks;

You get the chance,

  • to be part of a growing company with a unique business model;
  • to develop yourself in regulatory affairs with our team;
  • to adapt constantly and quickly to new products, processes, and projects;
  • to work in a flat structure and with flexible working hours.

 

Interested? We would like to get to know you. Send us your application file by e-mail to Beni Hirt, work@decomplix.com.

 

Offers from recruitment agencies will not be considered.

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