Join a dynamic team where your regulatory expertise will elevate product compliance and drive innovative solutions in the medical device industry. Collaborate cross-functionally to ensure swift approvals and optimal outcomes for patient care.

The Senior Software Engineer position at Globus Medical focuses on the development and maintenance of software applications and systems for intraoperative neuromonitoring. The role involves managing the entire software development lifecycle, collaborating with cross-functional teams, and ensuring compliance with industry regulations.

Discover innovative solutions as you lead engineering processes for product development, ensuring quality and efficiency from concept through FDA approval and market introduction. Collaborate cross-functionally to deliver cutting-edge medical devices.

Contribute to data-driven decision making by developing actionable insights, dashboards, and reports that enhance sales performance and operational efficiency in Robotics and Orthopedics, supporting commercial teams with vital analytics.

The Senior Regulatory Affairs Specialist at Globus Medical is responsible for drafting, submitting, and gaining clearance for FDA submissions, including 510(k) and IDE/PMA submissions for medical devices. This role requires collaboration with product development teams and a strong understanding of regulatory requirements to ensure compliance throughout the product lifecycle.