Regulatory Affairs Specialist I | Perú
Core
Support medical device regulatory activities by coordinating submissions, maintaining documentation, and managing product lifecycle activities including registrations and renewals for Andean markets.
Role type
Regulatory Affairs Specialist
Builds
Regulatory submissions and documentation for medical devices
Domain
Medical Devices / Healthcare
Required skills
Regulatory documentation management, Product lifecycle management, Cross-functional collaboration, Health authority communication, Organizational skills
Preferred skills
Andean market regulatory experience, Quality systems familiarity, Microsoft Excel proficiency
Technologies
Microsoft Excel