Regulatory Affairs Specialist I: Medical Device Submissions
Philips International
Philips seeks a Regulatory Affairs Specialist I to support global regulatory activities for Image Guided Therapy Devices. You will help ensure compliance with FDA, EU MDR, and other international requirements while collaborating with cross‑functional teams across the organization. This role provides exposure to documentation, submissions, lifecycle activities, and maintenance of technical files, with opportunities to grow in regulatory strategy and submissions across regions. #J-18808-Ljbffr Philips International
Vacancy posted 2 days ago
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