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QA Specialist

Full-Time Denmark , Europe
Health & Biotech
Health & Biotech
13 May 2024
  • Review and approval of several types of GMP documents related to laboratory equipment, IT and analytical methods (HPLC, Bio- and Immunoassay and general pharmacopoeia methods incl. microbiology).
  • Setting direction for the laboratory process groups across Novo Nordisk.
  • Support the development and validation of analytical- and microbial methods, both in-house and at our Contract Manufacturing Organizations.
  • Improving QC processes through engagement in projects implementing new technology and equipment, and active participation in Inspections from Health Authorities.
  • Have Master’s degree in a relevant field and carry extensive experience in the pharmaceutical industry.
  • Know how to independently identify and drive complex working assignments.
  • Engage in critical cases, set direction for projects and entry of new products where you safeguard the product quality and patient perspective.
  • Have an interest and talent for implementing strategy across BRD.
  • Have proficiency in both English and Danish.


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