Senior Medical Writer: Regulatory & Clinical Submissions Lead
Artivion, Inc.
Artivion, Inc. is a leading medical device company focused on cardiac and vascular solutions, based near Atlanta, GA. The role centers on writing regulatory documents, conducting literature reviews, and supporting MDR compliance through CEP/CER/PMCF activities. The successful candidate will collaborate with cross-functional teams, liaise with CROs and investigational sites, and help produce high-quality clinical documentation to support product maintenance and submissions. #J-18808-Ljbffr Artivion, Inc.
Vacancy posted 1 day ago
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