Chemical Engineer (MSc) with more than 20 years’ experience of the pharmaceutical industry within R&D, regulatory affairs, project management, strategic sourcing and supply chain. Main focus on CMC regulatory affairs for the past 14 years and currently as Global Regulatory Affairs Associate Director with drive to contribute to other’s development. Broad experience from CMC regulatory affairs, spanning from R&D to post-approval for both small molecules (synthetics) and biopharmaceuticals (biologics), covering both regulatory project management, strategies, and operations.MSc degree in chemical engineering with pharmaceutical science (Uppsala University) and project management with business focus (IHM Business School).