Senior Medical Writer, Regulatory Affairs (Medical Devices)
Artivion
Artivion, based in Kennesaw, Georgia, is seeking a professional to support the writing of clinical regulatory documents and ensure compliance with various regulations. This role involves collaboration across departments and oversees project timelines and budgets. Candidates should have at least 3-4 years of medical writing experience, a BS or MS in a relevant field, and strong communication and interpersonal skills. Artivion offers an opportunity to impact the medical device industry through creative solutions. #J-18808-Ljbffr Artivion
Vacancy posted 16 hours ago
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