Remote Post-Market Medical Device Safety Specialist
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Healthcare
Healthcare Compliance, Medical Device Industry, Medical Science
Job Description & How to Apply Below
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.
We are currently recruiting a Remote Post-Market Medical Device Safety Specialist for our team in North Chicago, IL, United States.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
This is a Full Time role.
The position is based in North Chicago, IL, United States.
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