David Pudwill Email & Phone Number
Vice President, Regulatory and Scientific Affairs, US @ Crossject
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David Pudwill Location
- Orlando, FL, US
David Pudwill Work
- Vice President, Regulatory and Scientific Affairs, US @ (August 2026 - Present)
- Principal Consultant @ (March 2024 - Present)
- Principal Consultant @ (April 2021 - Present)
- Professor @ (August 2020 - April 2021)
- President and CEO @ (April 2025 - Present)
- Instructor, Regulatory Submissions for Medical Devices @ (June 2024 - Present)
- Medical Sales Director @ (March 2023 - Present)
- Senior Vice President, Head of Regulatory Affairs @ (April 2021 - March 2023)
- Senior Director, Regulatory Affairs @ (September 2020 - April 2021)
- Senior Director, Ostomy Franchise Regulatory Affairs and Quality Assurance @ (November 2018 - August 2020)
- Director, Regulatory Affairs and Quality Assurance, Americas @ (January 2017 - October 2018)
- Lead Medical Device Reviewer, Biomedical Engineer @ (January 2008 - January 2017)
- Chief (Acting), Implantable Electrophysiology Devices Branch @ (November 2015 - April 2016)
- Congressional Affairs Specialist (Detail) @ (January 2015 - May 2015)
- Field Engineer @ (June 2006 - August 2007)
- Summer Research Intern @ (June 2005 - August 2005)
David Pudwill Education
- Harvard Business School Online
Other; "CORe: Credential of Readiness"
2016-2016 - The Johns Hopkins University
Master's degree (Mechanical Engineering)
2011-2014 - Case Western Reserve University
Bachelor of Science (BS) (Biomedical Engineering)
2002-2006 - Eastview High School
David Pudwill Skills
- Strategic Thinking
- Workload Prioritization
- Electronic Common Technical Document (eCTD)
- Pre-clinical Studies
- Analytical Skills
- Negotiation
- Written Communication
- Teamwork
- Resource Allocation
- Relationship Development
- Regulatory Agencies
- Oncology
- Immunology
- Clinical Trials
- ODD
- Pharmaceuticals
- Registration
- Asset Life Cycle Management
- Setting Strategic Direction
- Rare Diseases
- Regulatory Law
- Biotechnology
- Standard Operating Procedure (SOP)
- Pharmaceutics
- Good Manufacturing Practice (GMP)
- Lead Qualification
- Customer Satisfaction
- Attention to Detail
- Business Development
- Thought Leadership
- Strategic Leadership
- Critical Thinking
- Technical Documentation
- Regulatory Documentation
- QSR
- Presentations
- Marketing Compliance
- 21 CFR
- Management
- Leadership
- Leadership Development
- Project Management
- Engineering
- Product Development
- Data Analysis
- Biomedical Engineering
- Medical Devices
- FDA
- Clinical Research
- Public Speaking
- Cross-functional Team Leadership
- Policy
- Regulatory Affairs
- Health Policy
- Government
- Strategic Planning
- Research
- Team Leadership
- Photographic Lighting
- Photography
David Pudwill Summary
- David Pudwill, based in Orlando, FL, US, is currently a Vice President, Regulatory and Scientific Affairs, US at CROSSJECT. David Pudwill brings experience from previous roles at FDA Blueprint, Mr Regulatory and Prather Biomedical Corporation. David Pudwill holds a 2016 - 2016 Other; "CORe: Credential of Readiness" @ Harvard Business School Online. With a robust skill set that includes Strategic Thinking, Workload Prioritization, Electronic Common Technical Document (eCTD), Pre-clinical Studies, Analytical Skills and more. David Pudwill has 6 emails and 1 mobile phone numbers on RocketReach.
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