Kerstin Cleek is a seasoned professional in the field of quality assurance and engineering, with extensive experience at Roche since 2014 in various leadership roles, including Senior Quality Solutions Lead for Pharma Development and Principal Global Quality Technical Lead for Medical Devices. Key responsibilities encompass the implementation of the EU MDR and driving Pharma Quality System integration across the Roche Network. Kerstin also co-leads the Roche Global Health and Wellness Program, enhancing employee engagement across Europe and North America. Prior experience includes roles at Medtronic, where Kerstin contributed significantly as a Sr Design Assurance Engineer and Mechanical Design Engineer, focusing on quality management, risk assessment, and new product development. Kerstin holds a Master of Science in Bioengineering from the Technical University of Munich and a Bachelor of Science in Bioengineering from the University of California, Berkeley.
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