· Head of 12 projectmanagers (Scientists & Analytical Validation Managers)· Project Management department is responsible for all non-routine activities (validations, technology transfers etc.) & stability studies· Involved in quotation setup for new projects · Approval of deviations and OOS-investigations· Member of the Management Team, which is responsible for the Business Unit (headcount of 100)· Responsible for the budget & development of the lab together with the Manager QC · Acquiring new equipment· Approval of procedures, protocols and reports· Member of the deviation board, which treats complex deviations

· Supervisor of 9 QC-technicians· Scheduling of day-to-day activities· First contact in case of issues during analysis· Involved in hiring new labpersonnel· Responsible for the lab (headcount of 40) together with QC manager and 2 other teamleaders· First line in deviations and OOS investigations· Contact for clients about due dates and issues· Supporting in client and government audits

Quality control both on raw materials and end-products of pharmaceuticals. Including techniques are: • UV-Vis, • TLC• Dissolution • Potentiometry.• HPLC

Adjustments of standard operating procedures to a new quality system

Literature research in preparation of a research proposal.

Designing a lateral flow strip to detect melatonin in saliva with the use of up-converting phosphors.

Creating a toolbox for the design and development of microfluidic chips of PDMS.