Cydney Ryan, Ms
About Cydney Ryan, Ms
Cydney Ryan is a Senior Regulatory Affairs Specialist at Owlet Baby Care, where she has worked since 2022. She has a strong background in regulatory affairs, having held various positions in the field and earned degrees in Biomedical Sciences and Biomedical Regulatory Affairs.
Work at Owlet
Cydney Ryan currently serves as a Senior Regulatory Affairs Specialist at Owlet Baby Care, a position she has held since 2022. In this role, she has been involved in advising on labeling inputs and authoring verification protocols for medical devices. Prior to her current role, she worked as a Regulatory Affairs Specialist for three months in 2022 and as a Regulatory Affairs Associate for four months from 2021 to 2022. Her responsibilities at Owlet have included providing ongoing support in the design and development of an over-the-counter Software as a Medical Device (SaMD) for de novo submission to the FDA.
Education and Expertise
Cydney Ryan holds a Master of Science in Biomedical Regulatory Affairs from the University of Washington, which she completed from 2020 to 2022. She also earned a Master of Science in Biomedical Sciences from Texas A&M University in 2016, following a Bachelor of Science in Biomedical Sciences from the same institution in 2014. Her educational background provides her with a strong foundation in regulatory affairs and biomedical sciences, enhancing her expertise in the medical device industry.
Background
Before joining Owlet Baby Care, Cydney Ryan gained experience as a Regulatory Affairs/Quality Assurance Associate at Bio-Therapeutic from 2021 to 2022. She initially started at Bio-Therapeutic as a RAQA Graduate Intern in 2021. Her work involved leading regulatory strategy and authoring technical documentation for a Class IIb EU MDR/UKCA submission for a pediatric device. Additionally, she has experience as a Teaching Assistant for Biomedical Microbiology at Texas A&M University from 2014 to 2015.
Achievements
Cydney Ryan has contributed to various regulatory projects throughout her career. She has led the regulatory strategy for submissions and authored technical documentation for medical devices. Her work includes reviewing marketing and promotional materials for medical devices and consumer products. She coordinated third-party testing for compliance with IEC 60601 series requirements and ISO 10993. Furthermore, she supported Quality Management System (QMS) audits for successful certification of ISO 9001, IEC 62304, ISO 13485, MDSAP, and EU MDR.