Design, develop, test, and implement operating systems and software tools. Ensure system improvements increase efficiency and lead software lifecycle activities.

Provide technical, educational, operational, and sales support for cardiac rhythm management. Responsibilities include training, supporting medical device sales, and ongoing technical development.

Develops and conducts reliability studies, risk analyses, and performance reports for medical devices, recommending design changes to improve reliability.

The Commercial Leader for Slovakia will drive the country organization towards achieving strategic commercial objectives, overseeing sales, marketing, and operational efficiency while developing talent and relationships with key stakeholders.

The Senior Regulatory Affairs Specialist manages regulatory activities, prepares submissions, guides compliance, and collaborates with departments to ensure regulatory requirements are met for medical devices.

The Senior Logistics Supervisor will manage warehousing and distribution operations, ensuring compliance, team performance, and optimal delivery coordination.

The Informed Consent Specialist manages informed consent processes for clinical studies, coordinates internal and external stakeholder activities, and ensures compliance with regulatory approvals.

The Software Quality Engineer I supports quality engineering in medical device product development, ensuring compliance with regulations and leading risk management efforts.

The Manager, Pricing & Contracts Operations Transformation Lead drives the transformation of P&C Ops, ensuring effective execution, integration, and scalability across initiatives while managing global dependencies and performance metrics.

The Senior Data Analyst will collect and analyze large datasets, develop dashboards and reports, and collaborate with stakeholders to drive R&D performance insights.

Identify and mitigate patient safety hazards in software, conduct risk analyses for cardiac products, and ensure compliance with standards like ISO 14971.

The Technician will perform maintenance, inspections, and repairs on various machinery and equipment, using hand and power tools. Responsibilities include troubleshooting technical issues, leading technical processes, and ensuring operational efficiency through continuous improvement initiatives.

The Quality Systems Specialist will oversee quality programs, ensure compliance with regulations, conduct audits, and prepare documentation for internal and external stakeholders.

The Sr Regulatory Affairs Manager will lead global regulatory strategies, ensure compliance, and collaborate with teams for product approvals. Responsibilities include team management, regulatory agency interaction, and oversight of submissions for medical products.

The Category Manager-Electronic Assemblies will lead category strategies in electronics, negotiate supplier contracts, manage relationships, and optimize sourcing decisions to drive cost-effective solutions.

As a Principle IT Technologist - Scrum Master, you will lead testing strategies for PLM applications, ensuring quality across integrations while collaborating with teams in an agile environment.

As a Technical Sales Representative, you'll promote Medtronic's products, develop client relationships, conduct market research, and implement sales strategies to meet targets in a specified area.

The Sr Compliance Specialist develops compliance policies, provides advice, conducts investigations, maintains knowledge of compliance laws, and manages projects to align with legal standards.

As a Customer Specialist, you will manage surgical schedules, collaborate with hospital staff, and ensure timely delivery of patient-specific implants for cranial and spinal surgeries.

The Principal IT Architect is responsible for designing SAP-centric analytics and data platform solutions, ensuring alignment with enterprise architecture, collaborating with stakeholders, and leading technical initiatives within Global IT.