Un
Posted:
March 03, 2026
Location:
Ahmedabad, Gujarat, India
Job Description
Role Summary
Responsible for regulatory and quality activities for Class I & II medical devices, ensuring compliance with EU MDR, CE, and ISO 13485 requirements.
Key Responsibilities
Manage and maintain regulatory data (EUDAMED, MoH portals, internal systems).
Review regulatory and technical documentation for CE/MDR compliance.
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Apply Now Save for LaterJob Overview
Job Type:
Full-time
Location:
Ahmedabad, India
Posted:
March 03, 2026
Deadline:
April 12, 2026