Medical Technology Quality (M.S.)

Jacqueline Torfin

Jacqueline Torfin is currently Sr. Vice President of Regulatory, Quality, Clinical Research, and Reimbursement for CHF Solutions joining the company in October 2019. In this role, she is responsible for the global strategic quality and regulatory management in development, manufacturing and commercialization efforts. She also supports clinical research and reimbursement strategies to ensure maximum shareholder value.

Just prior to CHF Solutions she held the position of Vice President of Global Quality Assurance and Regulatory Compliance, as well as Data Protection Officer for NAMSA, a global medical device research organization (MRO) providing services including consulting, clinical research and laboratory services, with worldwide responsibility including the United States, Europe, and Asia.

Ms. Torfin has over 30 years and deep expertise in regulatory affairs, quality assurance and program management having worked for companies such as Beckman Coulter, CIMA Labs Inc, PDL BioPharma, Arizant Healthcare/3M, Logic PD and Heraeus Medical Components where she also served as Compliance Officer, head of contract management and the project management office for the global organization.

Her dedication to compliance extends to her role as an adjunct faculty member in St. Cloud State University’s Master of Medical Technology Quality and Regulatory Affairs and Services programs where in addition to teaching responsibilities, she was instrumental in the development of course curriculums.

Ms. Torfin holds a Bachelor’s Degree in Medical Technology from the University of Minnesota and a Master’s Degree in Leadership from Augsburg College. She is certified as a Quality Auditor through ASQ and as a notified body auditor for both Europe and Canada.

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