Jerker Åberg is currently the Director of Regulatory Affairs for Critical Care at Getinge, where they oversee the Regulatory organization for multiple site and product areas. They have previously held roles such as Regulatory Affairs Manager at Maquet Getinge Group and Acting Manager for Regulatory Affairs and Product Compliance. With a background in project management and product development, Åberg has extensive experience in regulatory affairs, international standardization, and quality management. They hold a Master of Science in Material Science with a focus on Polymers from Kungliga tekniska högskolan, which they completed in 1996.
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