Skills
Formulation Development, Process Development, Scale-Up Development, Validation as well as product(s) monitoring and yearly CPV (Continued Process Validation). Conduct Risk Assessment regarding any deviation/incident(s) to support final Quality Assurance decision regarding FDA (Food and Drug Administration) approved products. All of these different aspects require protocols and reports to be submitted to the FDA to support drug filing. Microsoft Word, Excel, PowerPoint, Minitab for statistical analysis of operating parameters as well as finished product results for submission the FDA. Ongoing production operator training regarding new processes or continued deviations/incidents accruing on the production floor.
About
My apologies, it seems that my resume is different version of Microsoft word, so the formatting may look funny.
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