Safety Specialist
Core
Conduct post-market safety management for medical devices to ensure patient safety and proper product use by collecting, evaluating, and reporting safety information globally.
Role type
Post-market safety specialist (medical devices)
Builds
Safety reports, risk assessments, and compliance documentation for medical device products
Domain
Healthcare / Medical Devices / Regulatory Safety
Required skills
Data collection and analysis, Regulatory compliance knowledge, Cross-functional collaboration, Document review and revision, Risk assessment participation, Trend analysis
Preferred skills
Medical device/pharma/healthcare industry experience, QA/PMS/GVP/QMS knowledge, Japanese Medical Practitioner qualifications, English email communication (TOEIC 650+), Data analysis experience