Joan Franklin
About Joan Franklin
Joan Franklin is a Senior Quality Assurance Specialist with extensive experience in quality management systems for medical devices. She has worked at several companies, including Boston Scientific and Magnolia Medical Technologies, and possesses expertise in IPC-A-610 standards, ISO 13485:2016, and FDA's cGMP regulations.
Current Role at Magnolia Medical Technologies
Joan Franklin currently serves as a Senior Quality Assurance Specialist at Magnolia Medical Technologies, a position she has held since 2023. In this role, she is responsible for ensuring the quality and compliance of medical devices. Her expertise in quality assurance is critical for maintaining high standards within the organization. Joan's previous role at Magnolia was as a Quality Manager, where she worked for 8 months. Her contributions in both positions support the company's commitment to quality in medical technology.
Previous Experience at Boston Scientific
Joan Franklin worked at Boston Scientific as a Senior Quality Assurance Specialist from 2019 to 2021. During her two years in Bothell, WA, she focused on quality assurance processes for electronic devices. Her experience with IPC-A-610 standards was essential in ensuring product quality and compliance within the electronics manufacturing sector.
Experience at EKOS Corporation
Joan Franklin held multiple roles at EKOS Corporation over a span of six years, from 2013 to 2023. She began as a Quality Assurance Specialist and advanced to the position of Senior Quality Assurance Specialist. Her extensive experience at EKOS contributed to her understanding of quality management systems, particularly in the medical device industry.
Educational Background
Joan Franklin studied at Washington and Lee University, where she earned a Bachelor's degree in Mathematics from 1989 to 1993. This educational foundation has provided her with analytical skills that are beneficial in her quality assurance roles within the medical device sector.
Expertise in Quality Management Standards
Joan Franklin possesses expertise in ISO 13485:2016, a standard that outlines requirements for quality management systems in medical devices. She is also knowledgeable in FDA's cGMP for Medical Devices, ensuring compliance with regulatory requirements. Her role as a MasterControl Sub Sysadmin and ComplianceWire Admin further demonstrates her involvement in managing document control and compliance training.