Stephanie Martinez

Senior Regulatory Professional | Cross-functional Team Leadership, FDA, EUMDR, International Regulatory Submissions, People Management

Role
Senior Regulatory Affairs Program Lead at Johnson & Johnson MedTech
Location
Milwaukee, WI, US
LinkedIn followers
500 followers
Healthcare & Human ServicesView LinkedIn profile

About Stephanie Martinez

At Eko, my role as a Senior Global Regulatory Specialist revolves around optimizing compliance processes and spearheading product submissions with a sharp focus on FDA and EU MDR regulations. My educational foundation in bioengineering from the University of Missouri-Columbia underpins my expertise in navigating the complex landscape of medical device regulations.My competencies in cross-functional team leadership have been instrumental in facilitating collaborations that enhance product submission success. Contributing to our team\'s achievements, such as the seamless preparation and submission of technical documentation, demonstrates my commitment to maintaining the highest standards of regulatory excellence.

Experience

  1. Senior Regulatory Affairs Program Lead

    Johnson & Johnson MedTech

    Jun 2024 — Present · Raritan, NJ, US

Education

  • University of Missouri-Columbia

    Bachelor's degree, Bioengineering and Biomedical Engineering

    2012 — 2016

Skills

  • Microsoft Office
  • Public Speaking
  • Facebook
  • Microsoft Word
  • Research
  • Time Management
  • Teamwork
  • Event Planning
  • Social Media
  • Powerpoint
  • Microsoft Excel

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Stephanie Martinez — Senior Regulatory Affairs Program Lead at Johnson & Johnson MedTech in Milwaukee, WI, US | Unifers