Margaret, Vice President and Head of Quality at Marengo Therapeutics, brings our team an impressive thirty-three years of pharmaceutical and biotech experience. For the past twenty-nine years, she has been a dedicated advocate for quality, with a particular focus on GxP regulations. Her expertise has led to the successful development and implementation of quality strategies, ensuring our compliance. Margaret’s belief in tailored systems that meet our company’s needs is a testament to her understanding of our unique challenges and goals.

Over the past six years, Margaret has led GxP Quality for two early clinical phase biotech companies, overseeing the implementation of electronic quality management systems. She has supported these companies in non-clinical studies, GLP studies, clinical protocol development, GMP manufacturing and testing, and preparation of IND filings. Before her role at Marengo, Margaret served as Inspection Lead at Shire, managing site readiness for regulatory agency inspections. She also led compliance programs at Sanofi and managed audit and recall programs at Takeda.

Margaret earned her B.S. in Biology, specializing in microbiology and biotechnology. She has continued her education with business studies, completing the Harvard Manage Mentor series and QP coursework. Additionally, Margaret has completed Operational Excellence and Lean Six Sigma Green Belt programs. Margaret’s extensive experience and collaborative nature will lead the Marengo team to the next level of quality and compliance.