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Laurel Christmann is a seasoned professional in regulatory affairs and quality assurance with extensive experience in the pharmaceutical industry. Currently serving as Director of Regulatory Affairs and Quality Assurance at Jazz Pharmaceuticals since March 2019, Laurel previously held the position of Associate Director in Quality/Compliance and Regulatory Affairs. Prior experience includes over 15 years at Biogen, where Laurel was Associate Director of Regulatory Affairs and also led Canadian Regulatory Affairs, Quality Assurance, and Pharmacovigilance teams. Laurel began the career at GlaxoSmithKline, contributing as Project Leader in Regulatory Affairs for vaccinations, and as Regulatory Affairs Manager at Glaxo Canada Inc., successfully preparing submissions and securing approvals for significant products. Laurel holds a B.Sc. in Toxicology (Biomedical) from the University of Guelph, obtained in 1988.