Pharmacovigilance Writer

Job Summary

A company is looking for a Pharmacovigilance Writer.

Key Responsibilities:

• Assess, follow-up, code, and manage vigilance activities for global complaints
• Author, peer review, and approve vigilance reports for regulatory submissions
• Collaborate with internal teams to ensure compliance with regulatory reporting standards

Required Qualifications:

• Bachelor's degree or relevant combination of education and experience
• Experience in medical device complaint triage and vigilance reporting
• Strong proficiency in MS Office and complaint database applications
• Knowledge of medical device Quality Management Systems
• Experience with global vigilance reporting requirements for medical devices