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The Staff R&D Engineer leads the design and development of new endovascular/neurovascular products, guiding cross-functional teams, conducting research, and ensuring manufacturability while meeting performance and cost targets.

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.

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.

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 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.

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.