Maya Butterfield
About Maya Butterfield
Maya Butterfield is a Senior Sales Representative at Primerica, where she has worked since 2016. She has extensive experience in the medical device industry, having held various roles in quality assurance and regulatory affairs, and holds a PhD in Mechanical Engineering (Bioengineering) from the University of Leeds.
Work at Primerica
Maya Butterfield has been employed at Primerica as a Senior Sales Representative since 2016. In this role, she focuses on providing financial services and solutions to clients. Her position involves engaging with clients to assess their financial needs and offering tailored products to meet those needs. The office is located at Suite 201-15290 103A Ave, Surrey, BC, V3R 7P8.
Previous Experience at Pyng Medical
Before joining Primerica, Maya Butterfield worked at Pyng Medical as the QA & RA Manager from 2006 to 2011. In this position, she was responsible for quality assurance and regulatory affairs, contributing to the compliance and safety of medical devices. Her tenure lasted for five years, during which she gained valuable experience in the medical device sector.
Experience at Emergo
Maya served as a Senior RA/QA Consultant at Emergo from 2011 to 2016. Her role involved providing regulatory and quality assurance consulting services to clients in the medical device industry. This five-year experience further enhanced her expertise in regulatory compliance and quality management systems.
Education and Expertise
Maya Butterfield holds a PhD in Mechanical Engineering (Bioengineering) from the University of Leeds, where she studied from 1988 to 1993. She also earned an MSc in Bioengineering from the University of Strathclyde in 1988 and a BSc in Science from University College Dublin from 1982 to 1986. Her educational background supports her extensive knowledge in regulatory strategies and compliance in the medical device industry.
Regulatory Experience and Achievements
Maya Butterfield has significant experience in the medical device industry, particularly in regulatory strategizing for Canada, the USA, and Europe. She has a proven track record of obtaining Health Canada Medical Device Licenses for Class II, III, and IV devices. Additionally, she has experience with FDA processes, including conducting 513(g), 510(k), and Q-Sub Meetings. She has also assisted clients in achieving ISO 9001:2015 certification within three months.