International Regulatory Affairs Specialist

• Create, submit and maintain product registration request for submission
• Review and approve documents required for submission
• Maintain up to date metrics with product registration request and submission schedule
• Track regulations applicable for medical devices in designated countries

Overview

• Industry - IT - INFORMATION TECHNOLOGY
• Functional Area - Regulatory Affairs / Corporate Affairs
• Job Role - Regulatory Affairs Specialist
• Employment type - Full Time - Permanent
• Work Mode - Hybrid

Qualifications

• Any Graduate - Any Specialization
• Any Post Graduate - Any Specialization
• Any Doctorate - Any Specialization

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