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Senior Regulatory Strategist, Medical Devices (Hybrid
Job Description & How to Apply Below
Location: Covington
Dormont Manufacturing Co. in the United States seeks a Senior Regulatory Affairs Specialist to lead U.S. and CE marking submissions and regulatory strategy across the product lifecycle.
You will collaborate cross-functionally to ensure compliance and drive submissions for medical devices. This role offers hybrid work with on-site days in Covington and one remote day per week, and travel up to 15% as needed; you will interact with auditors and regulatory bodies to support post-market activities
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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