Regulatory Affairs Specialist

• May perform multiple functions within the Postmarket surveillance department.
• Major responsibilities would include determining classification, review, and disposition of adverse events and medically related complaints for on-market products, including decisions on seriousness, reportability, and potential causality.

Overview

• Industry - IT - Consulting Services / Advisory Services
• Functional Area - Regulatory Affairs / Corporate Affairs
• Job Role - Lead Associate - Regulatory Affairs
• Employment type - Full Time
• Work Mode - In Office

Qualifications

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

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