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The Staff Software Test Engineer designs and executes test procedures for robotic medical software, ensuring compliance with regulatory standards and quality requirements.

The Sr Process Development Engineer will define, optimize, and validate manufacturing processes for neuro-interventional medical devices, while collaborating with cross-functional teams to improve equipment and document processes.

Lead pricing and contracting for GPOs, IDNs, and large health systems. Manage contract lifecycle using CLM platforms, maintain pricing governance and approval matrices, oversee chargeback/rebate reconciliation, operate RFP/RFI portals, support product launch pricing, and develop dashboards/KPIs to ensure compliance and revenue integrity while partnering with Sales, Finance, Legal, and Operations.

The ERP Systems Analyst II analyzes and supports ERP-related activities, collaborates with teams, troubleshoots systems, and assists in training for system implementation.

The Process Development Engineer I will optimize and validate processes for medical devices, support cross-functional teams, and ensure manufacturing quality standards.

The Sr Supplier Quality Engineer leads quality engineering support across medical device development and supplier performance improvements, ensuring compliance with regulations and driving supplier quality enhancements.

Lead process design and implementation of medical device production, ensuring effective methods and technologies are utilized for commercialization. Provide expertise and guidance on project management and compliance with quality systems.

The Principal R&D Engineer leads projects in catheter engineering, driving innovation, evaluating product designs, and mentoring team members. Responsibilities include ensuring manufacturability and compliance with quality systems.

Develop and test software applications for robotic-assisted technologies in healthcare. Collaborate with cross-functional teams, focusing on UI design, user requirements, and software architecture.

Lead the quality assurance function for robotics medical devices: build and maintain the QMS, ensure compliance with FDA and international standards, define regulatory strategy, oversee verification/validation and supplier quality, and grow/manage the QA team to support product transfer to manufacturing and commercial launch.