Browse 10 exciting jobs hiring in Eu Mdr now. Check out companies hiring such as NeuroLogica, Procept BioRobotics, Penske Truck Leasing in Ontario, Winston-Salem, Glendale.
NeuroLogica seeks a Senior Regulatory Affairs Specialist to lead global regulatory submissions and compliance for CT, X‑ray, ultrasound and AI-enabled imaging products.
Lead and manage medical device clinical trials for PROCEPT BioRobotics, overseeing site selection, monitoring, regulatory compliance, and data quality with significant domestic travel.
PROCEPT BioRobotics is hiring a Senior Supplier Quality Engineer to lead supplier assessments, audits, and corrective actions that ensure high-quality components and compliant manufacturing processes for its surgical robotics products.
ActiGraph is hiring a Senior Compliance Specialist to lead QMS and regulatory compliance activities across product development, post-market surveillance, and audits for their medical-grade wearable solutions.
Lead regulatory strategy and submissions for PROCEPT BioRobotics' surgical robotics products, guiding projects from development through market approval and post-market activities.
ResMed seeks a Senior Manager of Design Quality (Digital Product) to lead a product quality team and act as the primary QA representative for software and SaMD projects, ensuring design control, risk management and regulatory compliance.
Artera is hiring a Systems Engineer to lead requirements, risk management, system architecture, and usability engineering for its AI medical-device products.
Baxter is hiring a Vice President of Medical Affairs for Healthcare Systems and Technologies to drive medical strategy, clinical evidence generation, and cross‑functional leadership from its Deerfield, IL headquarters.
Experienced regulatory/quality professional needed to manage post-market surveillance, complaint handling, and global adverse event reporting for Kestra's cardiac device portfolio in a hybrid, Kirkland-based role.
Experienced materials professional needed to lead materials review and support regulatory and production teams for polymer-based medical devices.
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