Anna Mc Call
About Anna Mc Call
Anna McCall is a Validation Project Manager with a background in Biomedical Engineering. She has extensive experience in medical device design and project management, having worked at various companies including Polyzen, Inc. and Becton Dickinson.
Work at Barry-Wehmiller Design Group
Anna Mc Call currently serves as a Validation Project Manager at Barry-Wehmiller Design Group, a role she has held since 2022. In this position, she manages projects focused on the development and improvement of medical devices. Her responsibilities include ensuring compliance with industry standards and regulations, particularly in ISO 13485 and FDA environments. Prior to her current role, she worked as a Senior Validation Engineer at the same organization from 2020 to 2022, where she further honed her expertise in medical device validation.
Education and Expertise
Anna Mc Call earned her Bachelor of Science degree in Biomedical/Medical Engineering from North Carolina State University, where she studied from 2010 to 2014. Her educational background provides her with a solid foundation in medical device design. She possesses strong knowledge in the field, particularly regarding implantable and disposable devices. This educational experience, combined with her professional roles, has equipped her with significant expertise in managing projects related to medical device development.
Background in Medical Device Engineering
Prior to her current role, Anna Mc Call gained valuable experience as a Senior Process Engineer at Becton Dickinson (CareFusion) from 2014 to 2017. In this position, she focused on process improvement within the medical device sector. Following this, she worked at Polyzen, Inc. as a Process Engineer from 2017 to 2020, where she further developed her skills in engineering processes related to medical devices. Her background reflects a consistent focus on the medical device industry.
Professional Experience in Medical Device Development
Anna Mc Call has extensive experience working in ISO 13485 and FDA regulated environments, which are critical for the medical device industry. Her roles have involved managing projects that require adherence to stringent regulatory standards. This experience positions her as a knowledgeable professional in medical device development and improvement, with a specific focus on ensuring product quality and compliance throughout the project lifecycle.