Scientific Writer

Keyrus Biopharma


Create, reinforce or improve procedures and working instructions related to samples management (including samples for release, for stability or as reagents and standards) and stability processes.


  • Analyze the procedures in place, challenge the current situation and propose improvements;
  • Submit to the supervisor responsible of this process a written way of working;
  • Translate global guidelines into local procedure including the analysis of the impact;
  • Collaborate with the supervisor responsible of the specific team;
  • Ensuring the consistency and quality level of all documents that are issued.



  • Bachelors Degree in life science, biology, chemistry, biochemistry, pharmacology;
  • PhD is a plus.


  • Excellent level of spoken & written French;
  • Lean six sigma culture;
  • GMP;
  • Writing skills;
  • Ability to deal with complex scientific issues;
  • Positive attitude;
  • Flexible (adapting to changes within a project, i.e changes of priorities, increase/decrease of workload).


  • Experience in multicultural settings, diverse environments with respect to dynamics of human interaction;
  • Experience in pharmaceutical industry using GMP and SOP standards.

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