Experience

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  Pipeline biotech a/s

  Aug 2012 - Nov 2014

  - Responsible for assisting study directors in pre-clinical cancer studies with protocol and report writing. - Responsible for preparing data and reviewing study protocols/reports/SOPs - Responsible for Business development including market analysis, developing marketing material and canvassing sales.- Responsible for developing the Quality Management system As a graduate student, I worked as a Student Assistant at Pipeline Biotech which is a GMP/GLP regulated CRO that performs pre-clinical studies for cancer research. - Responsible for preparing data and reviewing study protocols/reports/SOPs

  • Scientific Assistant

    Aug 2014 - Nov 2014

  • Student Assistant

    Aug 2012 - Aug 2014
• 

  Aarhus university

  Oct 2012 - Mar 2013

  Student assistant

  Responsible for internships for both secondary and high school students. Tasks were planning and conducting laboratory exercises, teaching in theoretical Molecular Biology.

• 

  Aarhus university

  Aug 2013 - Feb 2014

  Student mentor

  Responsible for introducing exchange students to study life in Denmark and supporting with University onboarding, registration and housing.

• 

  Det grønlandske hus

  Sept 2013 - Dec 2013

  Student mentor

  Mentor and role model for a Greenlandic Molecular Biology student. My main function was to support with structuring and planning general study work as well as exam preparation.

• 

  Novo nordisk

  Dec 2014 - now

  QC Manager of 11 employees both professionals and lab technicians. - Responsible for analysis methods including ELISA, CLOT, SPR (Biocore), pH and Osmo. - Responsible for delivering analysis results for clinical trials of new haemophilia products and validation of new analysis methods for new products in Novo Nordisk BiopharmAchievements: - Optimised planning tool for lab analysis from a manual planning to automated forecast planning based on production demands- Implemented a visual planning tool for daily planning and prioritising of projects for professionals- Succeeded with employee engaged koyotaKATA on ELISA method and fostering a scientific and data driven learning environment. Show less Validation responsible on the ED2 project - designing and building a new FVII production facility placed in Kalundborg, Denmark. - Appointed project coordinator and validation responsible for the utility and main distribution work package- Key competences within validation from basic design to Installation Qualification (IQ)- Writing and updating validation documents (User requirement specification, Validation Plans, Supplier Qualification Plans, Quality Risk Management, test protocol and reports- Conducting Factory and Site Acceptance Test (FAT & SAT) and Installation Qualification (IQ)- Responsible for supplier training, supplier negotiations and supplier audits and alignment between work packages- eTIMS superuser - Selected for Biopharm High Potential and GROW (leadership talent development programmes). Show less

  • Senior Manager

    Sept 2024 - now

  • Associate Manager

    Apr 2022 - Aug 2024

  • Associate Manager

    Oct 2019 - Mar 2022

  • Associate Manager

    Mar 2019 - Sept 2019

  • Associate Manager

    Mar 2018 - Feb 2019

  • Chemist

    Dec 2014 - Feb 2018