Global Lead, Medical Device Vigilance & AE Reporting
Medline
Medline Industries, LP seeks a senior leader to drive Medical Device Vigilance and pharmacovigilance programs. You will oversee clinical evaluation, medical event management, ICSR processing, ADR reporting and postmarket safety to ensure global regulatory compliance. Travel to support inspections may be required. This role leads cross-functional teams, partners with QA/Regulatory, and ensures timely safety reporting across devices, drugs, and consumer products. #J-18808-Ljbffr Medline
Vacancy posted more than 2 months ago
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