Nermeen Abdel Aal
About Nermeen Abdel Aal
Nermeen Abdel Aal is a Senior Regulatory Affairs Specialist at Boston Scientific with extensive experience in medical device regulatory affairs in Canada.
Title
Nermeen Abdel Aal holds the position of Senior Regulatory Affairs Specialist at Boston Scientific.
Current Role at Boston Scientific
Nermeen Abdel Aal is currently employed at Boston Scientific as a Senior Regulatory Affairs Specialist in Mississauga, Ontario, Canada. She has been in this role since 2018, bringing extensive experience in medical device regulatory affairs to the company.
Previous Roles at Boston Scientific
Earlier in her career at Boston Scientific, Nermeen held various roles, including Senior Regulatory Affairs Specialist for 9 months in 2018, Regulatory Affairs Specialist II from 2016 to 2018, Regulatory Affairs Specialist I (Canada) from 2015 to 2016, and Regulatory Affairs Specialist I - International from 2013 to 2015. Her tenure at Boston Scientific also includes an internship as Regulatory Affairs Coordinator in 2013 in Mississauga, showcasing her progressive career in regulatory affairs.
Additional Professional Experience
Beyond her impactful career at Boston Scientific, Nermeen worked at CDW as a Purchasing Agent for 4 months in 2012 in Etobicoke. She also served as a Research Chemist at Radient Technologies Inc. from 2008 to 2011 in North York, Ontario, and as a Medical Writer Assistant (Internship) at BioPharma Services Inc. in 2008 in Toronto, Canada Area. Furthermore, she contributed as a Research Assistant in BioOrganic Chemistry at the University of Guelph from 2007 to 2008.
Education and Expertise
Nermeen Abdel Aal completed a Post Graduate Certificate in Regulatory Affairs from Humber College from 2012 to 2013. She also holds an Hon. BSc. in Biological Chemistry from the University of Guelph, completed in 2008. She has over five years of experience in medical device regulatory affairs, with a deep understanding of Canadian Medical Device Regulations and Canadian Food and Drugs Regulations. During her post-graduate studies, she developed a mock New Drug Submission (NDS) and Clinical Trial Application (CTA).
Regulatory Affairs Expertise
Nermeen has a proven track record in managing and submitting Canadian Medical Device Licence Applications for Class II, III, and IV devices. She is skilled in developing pre-compilation plans and strategies, estimating timelines, and assessing technical data. Her work has successfully achieved product registration in compliance with Canadian regulatory requirements.