Marie works as a Compliance Specialist at a leading pharmaceutical company and is responsible for compliance with demanding QA standards in the production of viral therapeutics for clinical trials. She acts as a central interface between Quality Assurance (QA) and Production to ensure that all specifications are consistently implemented.

Her responsibilities include the management of events and deviations, in which she develops quick solutions and preventive measures when irregularities occur. In the area of change management, Marie supports changes in production - from device qualification to careful documentation.

Marie's structured way of working ensures compliance with high quality standards, supports safe and efficient production and contributes significantly to the success of clinical trials with pioneering anti-viral medications.