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
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
Senior Regulatory Affairs Program Lead
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
- Microsoft Word
- Research
- Time Management
- Teamwork
- Event Planning
- Social Media
- Powerpoint
- Microsoft Excel
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