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... Role Summary: The Global Trade Compliance and Operations Lead will assist ... operating procedures, trainings, and formal compliance policies to ensure all North ... trade regulations. The Global Trade..
... operating procedures, trainings, and formal compliance and operational policies to ensure ... is required to ensure trade compliance and operational KPIs are met ... to ensure execution of day-to-day..
REGULATORY AFFAIRS SPECIALIST - Peripheral Vascular Health Peripheral Vascular Health therapies are a critical part of the Medtronic vascular portfolio, treating patients with a broad range of conditions, including Peripheral and ..
... Cardiac OR solutions (e.g., blood management, cannulae) Extracorporeal life support Coronary ... regulatory strategies, preparing U.S. and international submissions and obtaining and maintaining ... Regulatory Affairs Specialists (RAS) and..
... role as a **Sr Principal Compliance/Audit Specialist** you will have responsibility ... to determine the state of compliance to appropriate regulations and standards, ... risk assessments and/or audits/assessments and..
... unit Regulatory Affair Specialists and international regulatory staffs to provide regulatory ... CE Mark and support other international agencies as required by product ... with FDA and/or indirectly with..
... with FDA and indirectly with international regulatory agencies on most projects/products ... internal procedures to ensure continuous compliance with all regulatory requirements. Must ... IDE) Experience with FDA and..
... Record of Processing Activities (RoPA) Compliance Specialist will be responsible for ... changes in the Integrated Risk Management (IRM) instance of ServiceNow The ... Privacy Program in development and..
... Regulatory Affairs Specialists (RAS) and international regulatory staffs to provide regulatory ... for FDA and support other international agencies as required by product ... with FDA and indirectly with..
... strategies; preparing US, EU and international regulatory submissions; providing documentation for ... regulatory submissions; providing documentation for international submissions; supporting post-market regulatory compliance activities; evaluating proposed product changes .....
