Results-driven professional with a solid understanding of Medical Device Reprocessing (MDR) and compliance frameworks. Recently graduated, bringing hands-on experience in quality assurance and regulatory processes through academic projects and internships. Adept at conducting thorough risk assessments, preparing regulatory submission documentation, and collaborating effectively with cross-functional teams to ensure adherence to regulatory standards. Committed to leveraging strong analytical skills and a passion for healthcare innovation to support the development and approval of safe and effective medical devices. Dedicated to staying abreast of industry trends and regulatory changes to enhance compliance initiatives and drive continuous improvement.
4o mini
Computer literate can run Microsoft office and PowerPoint.
Attending Women Circle, ESL classes, YMCA, Kitchener, Current
My education and leadership skills have nurtured me as an expert in planning and implementation of health & hygiene projects at the grassroots community level. My numerous years of community mobilization, education and health experience in planning and operations in the field may contribute to the overall success of the organization.