Pratik Chaudhari Email & Phone Number
Principal Regulatory Affairs Specialist @ Medtronic Brain and Spine Therapies
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Pratik Chaudhari Location
- Austin, TX, US
Pratik Chaudhari Work
- Principal Regulatory Affairs Specialist @ (November 2022 - Present)
- Senior Regulatory Affairs Specialist @ (September 2019 - November 2022)
- Regulatory Affairs Specialist-III @ The Fountain Group( Client:- Avanos Medical) (April 2018 - September 2019)
- Regulatory Affairs Consultant @ The Fountain Group (Client: Abbott Vascular) (November 2017 - March 2018)
- Regulatory Affairs Specialist-III @ Select Source International (Client:- GE Healthcare) (April 2017 - November 2017)
- International Regulatory Affairs Analyst @ Select Source International (Client: Carefusion) (February 2016 - April 2017)
- Regulatory Affairs Associate @ ExterNetworks (Client: Zimmer Biomet) (September 2015 - February 2016)
- Research Assistant @ (September 2014 - May 2015)
- Student @ (August 2013 - May 2015)
- Engineering Intern @ Maxx Medical (June 2014 - August 2014)
- Summer Intern @ (June 2012 - June 2012)
- Analytical Engineer Trainee @ (January 2012 - February 2012)
Pratik Chaudhari Education
- University of Illinois Chicago
Master's degree (Biomedical/Medical Engineering)
2013-2015 - University of Mumbai
Bachelor of Engineering (B.E.) (Instrumentation Engineering)
2008-2012 - Regulatory Affairs Professional Society Online University
Regulatory Affairs Certificate (RAC): Medical Devices
2016
Pratik Chaudhari Skills
- Matlab
- Microsoft Office
- Medical Devices
- R&D
- Engineering
- Regulatory Affairs
- Microsoft Excel
- Instrumentation
- ISO 13485
- Biomedical Engineering
- PowerPoint
- Research
- Microsoft Word
- Teamwork
- Visual Basic
- Product Development
- MS OFFICE
- Biomechanics
- eCTD
- ISI Toolbox
- Biomedical Devices
- Team Management
- SharePoint
- Design Dossier
- CE marking
- Technical Files
- Team Center
- International Regulatory
- Risk Management
- Biocompatibility
- Regulatory Submissions
- Microsoft PowerPoint
- Research and Development (R&D)
- U.S. Food and Drug Administration (FDA)
- 510(k)
- Budget & Resource Planning
- Clinical Affairs
- Clinical Assessment
- Communication
- Corrective and Preventive Action (CAPA)
- Cross-functional Team Leadership
- Global Regulatory Compliance
- Health Authority Interactions
- IT Documentation
- International Logistics
- Leadership
- Medical Device Directive
- Medical Device Regulation (MDR)
- New Product Dev
- Oral Communication
- PMAs
- People Management
- Post Approval Studies
- Premarket Approval (PMA)
- Product Registration
- Product Strategy
- Project Management
- QSR
- Quality System
- Regulatory Agencies
- Regulatory Approvals
- Regulatory Audits
- Regulatory Compliance
- Regulatory Documentation
- Regulatory Requirements
- Regulatory Science
- Strategic Influence
- Strategic Planning
- Team Leadership
- Technical Documentation
- Written Communication
- C
- FoxPro
- Troubleshooting
- HTML
- Research and Development R&d
- Programming
- Java
- u.s. Food and Drug Administration Fda
- C++
- C#
- Research and Development
- u.s. Food and Drug Administration
Pratik Chaudhari Summary
- Pratik Chaudhari, based in Austin, TX, US, is currently a Principal Regulatory Affairs Specialist at Medtronic Brain and Spine Therapies. Pratik Chaudhari brings experience from previous roles at Smith & Nephew, The Fountain Group( Client:- Avanos Medical), The Fountain Group (Client: Abbott Vascular) and Select Source International (Client:- GE Healthcare). Pratik Chaudhari holds a 2013 - 2015 Master's degree in Biomedical/Medical Engineering @ University of Illinois Chicago. With a robust skill set that includes Matlab, Microsoft Office, Medical Devices, R&D, Engineering and more. Pratik Chaudhari has 1 emails and 6 mobile phone numbers on RocketReach.
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