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Intermediate R&D Scientist

Abbott

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Developed automated data analysis scripts and conducted comprehensive R&D, contributing to regulatory submissions for medical devices while ensuring adherence to design controls and standards.

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  • Developed lab procedures for FDA 510(k) submissions, utilized by operators to conduct experiments and generate analytical reports for in vitro medical devices.
  • Authored and validated SAS JMP scripts, automating data analysis procedures and enabling streamlined data interpretation for data analysts, scientists, and engineers.
  • Leveraged Big Data analytics and data visualization tools like SAS JMP 14, Minitab 18, R, Power BI, and Excel Analyze-It to derive actionable insights from experimental results.
  • Managed Design Control elements including Planning, Input Requirements, Outputs, Design Reviews, Verifications, Validations, Change Control, and Design History Files.