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Rasmus Kragh Sørensen

Senior Consultant

Quality control
Deviations / CAPA
Change control
Project Coordinating
Tech transfer
Process validation

Rasmus holds a Master of Science in Process technology from Aarhus University. He has 11 years of experience within the pharmaceutical industry from Novo Nordisk, and thus has extensive experience within GMP, compliance, quality assurance and validation of processes for medicinal products. Including process validation, qualification of process and process equipment, deviation management, as well as carrying out and documenting change requests on a larger and smaller scale.

Most recently, he has been lead for the quality assurance in implementing of new products and equpment in the Recovery facility AE  at Novo Nordisk in Kalundborg. For many years he has been product manager for various products in a close cooperation with the development department as well as Regulatory affairs and therefore has been at the forefront of implementing major changes to the processes, as well as building the process for a new product. Rasmus has participated in many audits and inspections, as presenter for various countries from the USA (FDA), DKMA (the Danish Medicines Agency) to South Korea, Russia and Turkey.

“I naturally look for smarter ways of doing things and I am not afraid to challenge existing procedures. I am outgoing and a team player, I see great value in being able to use each other's skills. I thrive in a varied everyday life, with contact with many professional groups and departments and with great diversity in the tasks. I am practical and solution-oriented and have yet to encounter a challenge that I have not been able to solve.”