Senior Regulatory Affairs Specialist – Medical Devices

Join a forward-thinking global medical device company as a Principal Specialist in Regulatory Affairs. In this pivotal role, you will manage regulatory submissions and strategies for innovative orthopedic products. Your expertise will directly impact the approval and clearance processes, ensuring compliance with FDA, EU, and Health Canada regulations. This is a unique opportunity to work in a dynamic environment focused on advancing medical technology and improving patient outcomes.

Enjoy a collaborative culture, competitive benefits, and the chance to make a significant difference in healthcare.
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