Sofia Gidlund is a highly experienced professional in the field of quality management and regulatory affairs, currently serving as the Director of Quality Standards & Documents at AstraZeneca since October 2023. Prior roles include Regulatory Affairs Manager at Wellspect HealthCare, where responsibilities encompassed regulatory compliance for medical devices, international product registrations, and support during product development and market launches. Previously, Sofia held various positions at Mölnlycke Health Care and Dentsply Implants, focusing on global audit programs and quality management systems. Early career experience includes multiple roles at Astra Tech, where responsibilities spanned quality audit management, CAPA management, document management, and laboratory engineering for dose validation and microbiological quality control. Sofia Gidlund holds a Master of Science in Bioengineering from Chalmers University of Technology and has further educational experience at Aix-Marseille University.
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