Become a pivotal member of Medtronic as a Regulatory Affairs Specialist. Focus on ensuring compliance and accelerating approvals for creative medical devices.You will lead the preparation of regulatory submissions and engage with agencies to facilitate timely approvals. This role involves collaboration with various experts to navigate challenges and recommend compliance strategies. Your efforts will directly impact patient care by ensuring that high-quality products meet regulatory standards.Key Responsibilities:Coordinate document preparation for regulatory applicationsIdentify compliance needs for product changesCollaborate with teams to tackle regulatory inquiriesConduct audits and maintain systems for regulatory trackingFoster relationships with regulatory agencies for effective communicationRequirements:Bachelor's degree requiredMinimum of 2 years in regulatory affairsExperience with Health Canada is a plusProficient in project management and analytical tasksStrong verbal and written communication skillsUtilize your regulatory expertise to enhance healthcare impact at Medtronic.