Tina Ariaee, Ms, Rac
About Tina Ariaee, Ms, Rac
Tina Ariaee is a Director of Regulatory Affairs with extensive experience in the medical device and pharmaceutical industries. She has held various regulatory roles at companies such as Edwards Lifesciences, Allergan, and MicroVention, and she holds a master's degree from Louisiana Tech University.
Current Role at ReShape Lifesciences
Tina Ariaee serves as the Director of Regulatory Affairs at ReShape Lifesciences Inc. since 2021. In this role, she oversees regulatory compliance and strategy, ensuring that the company's products meet all necessary regulations and standards. Her expertise in regulatory affairs contributes to the development and approval of innovative medical solutions within the organization.
Previous Experience in Regulatory Affairs
Prior to her current position, Tina Ariaee held several significant roles in regulatory affairs. She worked at Edwards Lifesciences from 2008 to 2015 as a Senior Principal Project Manager, focusing on regulatory strategies. Afterward, she joined Alcon, a Novartis company, as Global Director of Regulatory Affairs for one year in 2015. Additionally, she served as Senior Manager of Regulatory Affairs at Microvention since 2017 and briefly at KaVo Kerr in 2017.
Quality Assurance Background
Tina Ariaee has a solid foundation in quality assurance, having worked at Allergan as a QA Manager from 2006 to 2008. Her experience in quality assurance complements her regulatory affairs expertise, allowing her to ensure that products not only meet regulatory standards but also adhere to quality protocols.
Educational Qualifications
Tina Ariaee earned both her Bachelor of Science and Master's degrees from Louisiana Tech University. Her educational background provides her with a strong foundation in the scientific principles that underpin her work in regulatory affairs and quality assurance.
Career Timeline
Tina Ariaee's career spans multiple roles in regulatory affairs and quality assurance. She began her career at Allergan as a Microbiology Senior Professional from 1995 to 2000, followed by various positions including Senior Regulatory Specialist from 2000 to 2006 and QA Manager from 2006 to 2008. After her tenure at Edwards Lifesciences, she continued to build her career in regulatory roles at Alcon, Microvention, and KaVo Kerr before joining ReShape Lifesciences.