Suzanne M.
About Suzanne M.
Suzanne M. is a Senior Regulatory Affairs Specialist at Inari Medical, where she has worked since 2022. She has extensive experience in regulatory affairs, having held positions at AbbVie, Vyaire Medical, Hospira, and Abbott Laboratories.
Work at Inari Medical
Suzanne M. has been employed at Inari Medical since 2022, where she serves as a Senior Regulatory Affairs Specialist. In this role, she is responsible for ensuring compliance with regulatory requirements and facilitating the approval process for medical devices. Her expertise contributes to the company's mission of advancing innovative solutions in the medical field.
Previous Experience in Regulatory Affairs
Before joining Inari Medical, Suzanne M. worked at Vyaire Medical as a Regulatory Affairs Associate from 2016 to 2021. Her responsibilities included managing regulatory submissions and maintaining compliance with industry standards. Prior to that, she held a similar position at Hospira from 2014 to 2016, where she also focused on regulatory compliance and documentation.
Experience at AbbVie
In 2016, Suzanne M. briefly worked at AbbVie as a Regulatory Technical Writer for one month. During this time, she contributed to the preparation and review of regulatory documents, enhancing her skills in technical writing within the regulatory framework.
Background in Chemistry
Suzanne M. began her career at Abbott Laboratories, where she worked as a Chemist III from 2006 to 2011. In this role, she conducted laboratory research and analysis, gaining valuable experience in the scientific aspects of product development and quality assurance.