Medical Device Vigilance Report Writer
A company is looking for a Global Product Monitoring Vigilance Report Writer (Remote/Flexible).
Key Responsibilities:
Assess, follow-up, code, and manage vigilance activities for global complaints
Author, peer review, and approve vigilance reports for timely regulatory submissions
Collaborate with internal teams to ensure compliance with regulatory reporting standards
Required Qualifications:
Bachelor's degree or equivalent relevant education and experience
Minimum of 3 years in medical device complaint triage and vigilance reporting or clinical experience in diabetes management
Experience in writing and filing global vigilance reports in the medical device industry
Knowledge of global vigilance reporting requirements and regulatory bodies
Preferred qualifications include a BSN with diabetes experience or certification as a Registered or Licensed Dietician or Diabetic Educator
A company is looking for a Global Product Monitoring Vigilance Report Writer (Remote/Flexible).
Key Responsibilities:
Assess, follow-up, code, and manage vigilance activities for global complaints
Author, peer review, and approve vigilance reports for timely regulatory submissions
Collaborate with internal teams to ensure compliance with regulatory reporting standards
Required Qualifications:
Bachelor's degree or equivalent relevant education and experience
Minimum of 3 years in medical device complaint triage and vigilance reporting or clinical experience in diabetes management
Experience in writing and filing global vigilance reports in the medical device industry
Knowledge of global vigilance reporting requirements and regulatory bodies
Preferred qualifications include a BSN with diabetes experience or certification as a Registered or Licensed Dietician or Diabetic Educator