Skilled Biopharmaceutical Professional with significant contract manufacturing experience in R&D and cGMP operations including Tech Writing, Validation, Quality Assurance, and Business Development. Expertise in tech transfer project supervision and execution through depth filtration, column chromatography and TFF at both lab and pilot scale. Subject matter expert in cGMP suites. Accomplished author of critical department documentation and technical reports. Proficient in creating internationally-used electronic Operational Excellence tools using Excel and Visual Basic. Business Development Manager with experience writing proposals for R&D and cGMP activities with microbial or mammalian hosts.