Paloma de Miguel

Paloma De Miguel has extensive work experience in the field of regulatory affairs, particularly within the pharmaceutical industry. Starting in 1989, they held multiple roles at Baxter Healthcare, including Vice President of Regulatory Affairs - International and Vice President of Regulatory Affairs EMEA. Paloma also served as Vice President of Global Regulatory Affairs Bioscience and Director of Regulatory Affairs Europe-Hyland Immuno during their time at Baxter Healthcare. In 2015, they transitioned to Baxalta, where they served as Vice President of Regulatory Affairs International. In 2017, Paloma founded Sacmis RA and worked as a Regulatory Affairs Consultant until 2018. Currently, they are the Chief Medical and Regulatory Affairs Officer at Kedrion Biopharma, where they previously served as the Senior Vice President of Global Regulatory Affairs.

Paloma De Miguel has attended the University of Valencia and pursued a PhD in Biology. No specific start or end years for these education experiences are provided.