Soumya N.
Manager, Regulatory Submissions Project Management at Regeneron Pharmaceuticals, Inc.
- Role
- Manager, Regulatory Submission Project Management at Regeneron
- Location
- Tarrytown, NY, US
- LinkedIn followers
- 500 followers
About Soumya N.
I am a forward-thinking pharmaceuticals industry professional with solid portfolio of success driving regulatory affairs, quality assurance, audits, and laboratory research & testing for pharmaceutical organizations. I have expertise in Code of Federal Regulations Title 21 related to pharmaceuticals, dietary supplements, and FDA, ICH, and USP quality requirements. I am a member of the Regulatory Affairs Professional Society. My areas of expertise include:Regulatory Affairs Quality Assurance Management Research & Development Audit Preparation Team LeadershipProtocol, Method & SOP DevelopmentRegulatory Compliance Current Good Manufacturing PracticesProject Management Data Analysis
Experience
Manager, Regulatory Submission Project Management
Jan 2026 — Present · Tarrytown, NY, US
Education
Northeastern University
Master of Science - MS, Regulatory Affairs
New York University
Master of Science - MS, Biotechnology
2006 — 2008
RAPS Online University
Regular Affairs Certificate, Medical Devices and Pharmaceuticals (Dual)
2014 — 2014
St. John's University
Bachelor, Biology
2003 — 2006
John Bowne High School
Diploma
2000 — 2003
Arizona State University
Doctor of Professional Practice, Regulatory and Clinical Research Management
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