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Scientific Writer

Keyrus Biopharma

Belgium

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.

KEY RESPONSIBILITIES

  • 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.

Profile

Education:

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

Knowledge:

  • 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:

  • 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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