Teams at Noah Medical

Lead the strategy for robotic-assisted platforms by identifying clinical needs, developing business plans, and ensuring product readiness for market launch.

Lead regulatory strategy and submissions for medical devices, support cross-functional teams on design and manufacturing changes, prepare FDA 510(k) and international dossiers, ensure compliance with FDA, EU MDR, ISO standards, review labeling/promotional materials, support audits/inspections, and provide regulatory guidance for post-market activities.

Support and improve the Quality Management System for a medical robotics company: manage CAPAs, investigations, change control, document control, audits, data trending, and inspection readiness while partnering cross-functionally to ensure compliance with FDA and ISO standards.