Remote Post-Market Medical Device Safety Specialist
Actalent
Actalent is seeking a dedicated Medical Device Safety Reviewer to collect, review, and process complaints and reports related to medical device adverse events in clinical studies, ensuring compliance with 21 CFR parts and FDA guidance.
The role focuses on post‑market safety, risk management, and supporting audits. It is remote with CST-aligned hours, contract from North Chicago, IL, and offers extensive benefits for a temporary role.
#J-18808-LjbffrVacancy posted 3 days ago
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