Sean O’bryan
Vice President of Regulatory Affairs and Quality A
Bioinformatics & Systems Biology
Lysogene
France
Biography
Sean is responsible for providing global regulatory strategic leadership and for the creation and maintenance of quality systems assuring global compliance. Prior to joining Lysogene, he was the Director of Regulatory Affairs at bluebird bio leading efforts on the treatment of the rare disease CCALD through LVV gene therapy where he initiated and led the RA CMC group across all programs including CNS, hematology and oncology. Prior to this, he worked 8 years at Genzyme/Sanofi serving as a global regulatory lead for the Cell Therapy and Regenerative Medicine division. Sean has more than 20 years of regulatory experience across a range of categories including biologics, gene therapy, chemistry, manufacturing and control (CMC) and medical device Sean holds a BS in Biology and Analysis and Policy from Boston University and is RAPs certified.
Research Interest
Bioinformatics & Systems Biology
