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Paul Nitschmann Location
Moorpark, CA, US
Paul Nitschmann Work
SVP Regulatory Affairs @ (August 2025 - Present)
Member @ (January 2025 - Present)
SVP Regulatory Affairs @ (November 2024 - August 2025)
SVP Regulatory Affairs @ (May 2021 - August 2025)
Head of Global Regulatory Affairs Execution Team (Reg Ops, Labeling, Writing, Resourcing) @ (February 2021 - May 2021)
Exec Dir, Reg TA Head, CV, CNS, Bone, NonOnc Hematology, Head Reg Labeling, Resource Mgmt, Reg Ops @ (August 2020 - February 2021)
Executive Director, Regulatory TA Head, CV, CNS, Bone, Head Global Labeling, Interim Head Reg Ops @ (December 2016 - August 2020)
VP, Head BD and L and Early Develpment (NIBR) Regulatory Affairs @ (November 2015 - December 2016)
VP, Head of Regulatory Affairs Pharmaceuticals @ (September 2010 - November 2015)
Senior Director North America Regulatory Affairs @ (October 2009 - September 2010)
Senior Director, Regulatory Portfolio Leader Primary Care CNS @ (September 2008 - October 2009)
Senior Director, Strategy Line Manager @ (December 2003 - September 2008)
Director Regulatory Affairs @ (May 1998 - December 2003)
Clinical Regulatory Project Manager @ (November 1994 - May 1998)
Medical Advisor @ (February 1991 - November 1994)
Paul Nitschmann Education
Erasmus Universiteit Rotterdam
M.D. (M.D., Medicine)
1977-1984
Erasmus University Rotterdam
M.D. (Medicine)
1977-1984
Het Rhedens Lyceum 1970-1977
Paul Nitschmann Skills
Pharmaceutical Industry
Regulatory Affairs
Clinical Research
Clinical Development
Clinical Trials
GCP
Neuroscience
Anesthesiology
Ophthalmology
Drug Development
Biomarkers
Pharmaceutics
FDA
Biopharmaceuticals
Drug Discovery
Lifesciences
Medical Writing
Endocrinology
Medicine
Pharmacovigilance
Gastroenterology
Pharmacology
IND
Strategy
Translational Medicine
Neurology
Clinical Pharmacology
Medical Devices
Market Access
Regulatory Submissions
Cardiology
Medical Affairs
CRO
Health Economics
Therapeutic Areas
Regulatory Requirements
Infectious Diseases
Life Sciences
Biotechnology
CRO Management
Good Clinical Practice (GCP)
U.S. Food and Drug Administration (FDA)
Sales
Product Launch
Research
Marketing
u.s. Food and Drug Administration Fda
Good Clinical Practice Gcp
Good Clinical Practice
u.s. Food and Drug Administration
Paul Nitschmann Summary
Paul Nitschmann, based in Moorpark, CA, US, is currently a SVP Regulatory Affairs at Zydus Therapeutics. Paul Nitschmann brings experience from previous roles at ISPEP, Alfasigma, Intercept Pharmaceuticals and Amgen. Paul Nitschmann holds a 1977 - 1984 M.D. in M.D., Medicine @ Erasmus Universiteit Rotterdam. With a robust skill set that includes Pharmaceutical Industry, Regulatory Affairs, Clinical Research, Clinical Development, Clinical Trials and more. Paul Nitschmann has 4 emails and 4 mobile phone numbers on RocketReach.
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