Description
- 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.
Qualifications
- 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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