Analog Devices, Inc. seeks a Regulatory Affairs Specialist in Limerick, Ireland. This role is integral to the Digital Healthcare Group, focusing on developing monitoring solutions. The specialist will provide strategic regulatory guidance, manage submissions (Pre-Sub, 510(k)), and ensure compliance with FDA and ISO 13485 standards. A Master's in Regulatory Affairs and experience with FDA regulations are required. This full-time position may require up to 10% travel.
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