regulatory affairs associate international (100% m/w) in Schaffhausen

schaffhausen, schaffhausen
life sciences
job type
reference number
yannick rieger, basel professionals it & life sciences
058 201 55 50
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job description

Your responsibilities:
  • In collaboration with the Global Regulatory Team and the local quality assurance, you create and update registration documents (like DMFs, eCTD ) at an international level
  • You prepare, submit and follow-up registration files (new products/indications, modifications..)
  • You are in regular contact with authorities and customers and support on registration requests.
  Your skills:
  • You have a scientific degree ( for example, chemicals, pharmaceuticals ) and
  • You have professional experience in cGMP environment and in the areas of authorization / registration
  • You have a good knowledge about regulations in the pharmaceutical industry
  • You are fluent in German and English
  • You are a conscientious and have a structured way of working as well as high
  • You are a good team player
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