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The Senior Reliability Engineer will conduct technical reliability studies, recommend design and test methods, complete risk analysis, analyze performance reports, and ensure corrective measures meet reliability standards.

As a Senior Signal Processing Engineer at Medtronic, you will develop signal processing algorithms for real-time medical applications, collaborate with hardware teams, and oversee software integration for heart rhythm disorder treatments.

The Principal Contract Analyst at Medtronic is responsible for providing contracting support for the CRDN Operating Unit, coordinating physician engagement, partnering with the legal team to draft contracts, managing contract documentation, and processing requests and payments. The role requires strong financial and analytical skills and involves collaboration with internal and external clients.

As a Senior Principal Aortic Sales Representative at Medtronic, you will be responsible for achieving sales revenue targets, managing territory effectively, developing accounts, building customer relationships, and promoting medical technologies. You will educate medical staff on products and navigate a highly competitive sales environment, ensuring excellent customer service and product knowledge.

The Sales Representative I for Medtronic is responsible for soliciting orders and selling spinal products, managing inventory, maintaining customer records, and meeting sales quotas within a designated territory. This field-based role involves account management, customer interaction, and compliance with Medtronic policies.

Manage a team overseeing Medtronic’s surveillance program, ensuring compliance with regulations and effective report management. Utilize project management skills to lead cross-functional teams, implement improvement methodologies, and develop standardized approaches for operational excellence.

In this role, the Principal MDR/Vigilance Specialist will manage a team monitoring Medtronic’s surveillance program, handling adverse reports and compliance with regulations. Responsibilities include developing processes for regulatory reporting, evaluating projects, and ensuring adherence to medical device reporting requirements.