Wrote publications for physician audiences including manuscripts, abstracts, posters, slide presentations
Presented at various educational, local, and national medical conferences
Reviewed research protocol design and reports for physician and scientific community audiences

-Authored over 15 validation protocols and reports for critical equipment and systems.
-Contributed authorship and review of source documents for CMC as part of the technical regulatory dossier for filing to regulatory agencies.
-Collaborated with cross-functional project teams to address validation, quality, technical, and regulatory issues pertaining to the vaccine manufacturing processes, ensuring compliance with cGMP regulations.

Assessed patient vital signs and performed EKG's
Started IV's and collected blood samples for lab processing
Assisted with trauma levels 1, 2, and 3 in coordination with trauma physician
Responsible for efficient patient documentation and charting practices

Assessed the quality of generic on-the market drugs for their effectiveness in different conditions
Made use of dissolution apparatuses, gas chromatography machines, and high performance liquid chromatography machines to ensure accurate drug manufacturing quality in testing for specific active pharmaceutical ingredient (API) performance over a 24 hour period
Responsible for compliance with FDA standards of laboratory protocol