Manager, Regulatory Operations - Regulatory Data Management (Devices)

What you’d do

Manage regulatory operations projects and a team handling dossier preparation, clinical trial disclosure, submission management, publishing, licensing, and labeling for medical devices. Full time role ensuring timely, compliant submissions under GxP and SOPs. Found on the employer's careers page on Oct 3, 2026. Apply through the link.

You’ll need

• Expertise in regulatory submission lifecycle for Class I, II, III devices
• Experience with US, EU, and Canada submissions
• Team management and supervision experience
• Project management and problem-solving skills
• Knowledge of GxP regulations and SOPs