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.
