Diligent, engaging, and efficient Regulatory Affairs Specialist within the Medical Device Manufacturing Industry offering 8+ years of progressive experience and measurable accomplishments in the field. Expert at providing key leadership and training to st

In reviewing the attached résumé, you will note that I possess over 8 years experience assuming progressive roles from a Research Associate to an Associate Research Scientist. My keen knowledge and understanding of R&D and Regulatory Affairs to contribute to the design and preparation of non-clinical study protocols, as well as the design, initiation, monitoring, and close-out of studies for stability and validation of all company products on a global scale will prove to be beneficial. I work well with a host of personnel from international companies that has included Biopharmaceutical, Hospital, Transfusion, and Veterinary Medicine entities throughout the U.S., Europe, Asia, Latin America, and Middle East.

Life Scientist

Diamond Bar, CA