Intuitive in Mexicali, Mexico, is seeking an experienced regulatory professional to support post-market strategies and reporting for its surgical devices. This onsite role collaborates with Regulatory Affairs, Quality, and Medical teams to ensure compliance with post-market requirements.
You will develop PMS Plans and PSURs, summarize data for clear dashboards, and help prepare regulatory submissions. Advanced English and STEM degree are required, with 5+ years in medical device regulation.