Teams at iRhythm Technologies

Lead the validation and compliance of non-product software used in medical device development. Responsibilities include defining validation strategies, ensuring compliance with FDA and ISO standards, and cross-functional collaboration.

The manager will develop regulatory strategies for medical devices, manage a regulatory team, lead FDA submissions, and ensure compliance with global regulations.

The Technical Project Manager will lead lifecycle projects for medical devices, ensuring compliance, project planning, execution, and collaboration across teams while improving product quality.