Regulatory Affairs Manager (Irvine)

Regulatory Affairs Manager (Hybrid Preferred)

📍 Location : Irvine, CA | 💼 Full-time | 🏥 Medical Device Industry

Join a passionate, mission-driven team dedicated to advancing medical device innovation and improving patient outcomes. As a Regulatory Affairs Manager , you will play a key role in coordinating and preparing regulatory submissions, partnering with cross-functional teams, and ensuring compliance with global regulatory standards. This role offers the opportunity to apply your expertise in a collaborative environment while directly contributing to life-saving technologies.

What Youll Do

• Develop and implement complex, global regulatory strategies for new and modified devices.
• Prepare, review, and submit regulatory documentation for the U.S. and international markets.
• Serve as the regulatory representative on multi-disciplinary project teams, aligning regulatory strategy with business objectives.
• Interact with FDA, Notified Bodies, and international authorities throughout the device lifecycle.
• Review product changes, labeling, advertising, and promotion for compliance with applicable regulations.
• Support ongoing product maintenance, license renewals, and annual registrations.
• Provide regulatory guidance during audits, inspections, and SOP development.
• Consolidate and maintain communication with regulatory agencies and cross-functional stakeholders.

What Were Looking For