I am hiring for a 1-year contract role for an RA Associate. There is some opportunity for a contract extension, or a possible conversion to full-time, but it's not a guarantee.
The role would primarily focus on Regulatory Intelligence for our organization, but would have secondary responsibilities helping support 510(k) and IDE submissions. There's also an opportunity to help support a De Novo for a FDA breakthrough device. This role will gain experience in digital health, SaMD and other exciting and growing areas in the medical device field. If you know of anyone that is entry-level RA , or looking to break into the RA field with some already existing medical device knowledge, please send me a message. I'd love to discuss this opportunity more.
The role is either based out of St. Paul, Minnesota or in the San Franscisco Bay Area. 3-days in office, 2 days WFH.
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Katherine Doll Kanne
Principal Regulatory Affairs Specialist
Saint Paul MN
United States
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