Aldo Roblero
Process Development Associate at Vital Bio
Based in Toronto, Canada
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Seniority
Staff
Department
Research & Development
Location
Toronto
Industry
Biotechnology Research
Company size
223
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a•••••••@vitalbio.com
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Background
About Aldo Roblero
cGMP and ISO 13485, 21 CFR Part 820 trained, experience working within ISO 9001 eQMS. Inquisitive, diligent, strategic, and open-minded, with 2 years of Pharmaceutical Manufacturing experience, I have produced SOPs for various processes. determined Quality Control thresholds, verify reproducibility of reagent/QC processes as well as iterate and improve on various manufacturing operations throughout my career. My current objective is to investigate, establish, and enforce Critical Material Attributes, Critical Process Parameters, Root Cause Analysis, Process Failure Mode and Effects Analysis, as well as Quality by Design, while adhering to FDA, Health Canada requirements. In doing so, I generate and consolidate reliable, reproducible, and robust high-value materials/process that support Immunoassay development and performance within various biomedical diagnosis systems.
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