Izzy Monroy

Background

About Izzy Monroy

Over 15 years of combined professional experience in biotechnology, medical device manufacturing, R&D, GDP, GMP, GLP standards, and data storage infrastructure-Over 12 years of documentation control/configuration management under ISO 13485 and 21 CFR Part 820 - Possesses the time management skills necessary for the oversight of numerous ongoing projects at various stages of development, validation, prototype, production, to end of life- Possesses a keen mind and excellent troubleshooting skills with a strong ability to identify risks and assess and manage their impact- Ability to communicate effectively with a diverse range of customers and stakeholders- Ability to be flexible and achieve results in a fast-paced, deadline-driven work environment. Skilled in EDMS Systems (Teamcenter, Livelink, Agile, Veeva, and QCBD), ERP Systems (SAP and Oracle), Windchill, Asana, JIRA, Confluence, Sharepoint, Google Documents, Visio, Everest, Quickbase, Microsoft Office Suite, Outlook, Quickbooks, Adobe Acrobat, and PowerPoint.