Senior Regulatory Affairs Lead, Medical Devices Submissions
Listed on 2026-10-16
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Healthcare
Healthcare Compliance, Medical Science Liaison
Lance Soft is seeking a Senior Regulatory Affairs Specialist to plan, coordinate, and report on regulatory programs for Beckman Coulter products. The role focuses on post-market activities, complaint management, and global compliance strategies.
Responsibilities include preparing regulatory submissions (510(k), PMA) and coordinating cross-functional teams to support product labeling, data structuring, and promotional materials review.
We are currently recruiting a Senior Regulatory Affairs Lead, Medical Devices Submissions for our team in Chaska, MN, United States.
Our team is growing, and we are hiring a Senior Regulatory Affairs Lead, Medical Devices Submissions in Chaska, MN, United States.
This opportunity is for the Senior Regulatory Affairs Lead, Medical Devices Submissions role at Lancesoft.
We are seeking a motivated Senior Regulatory Affairs Lead, Medical Devices Submissions to join Lancesoft in Chaska, MN, United States.
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