Director, Regulatory Affairs

Ocugen is seeking an experienced Director, Regulatory Affairs to lead regulatory strategy and execution for innovative gene therapy products and Advanced Therapy Medicinal Products (ATMPs) across the European Union and United Kingdom. This role involves providing strategic regulatory guidance from early development through clinical development, marketing authorization, and post-approval activities. The position requires significant responsibility for advancing Ocugen’s clinical-stage programs toward European registration, including preparation for Marketing Authorization Application (MAA) submissions.