Maya Szabo is a Regulatory Affairs Lead with over 15 years of experience in the generic pharmaceutical industry. They have specialized in regulatory strategy, cross-functional project management, and compliance, demonstrating proven leadership in managing high-performing teams across global markets. Maya has held several key positions at Teva Pharmaceuticals, including Sr. Director of Gx Strategy & New Submissions, and has been responsible for regulatory strategy and project management in various growth markets. Currently, they serve as a Regulatory Affairs Lead at PolyPid Ltd. Maya holds an MBA focused on biomedical companies and two bachelor's degrees in social sciences and life sciences from The College of Management Academic Studies and Tel Aviv University, respectively.
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