Medical Device Risk Management Advisor
Job reputed company:
• Test new features and prototypes periodically
• reputed company feedback on usability and regulatory alignment
• Review risk management and documentation workflows
• Suggest improvements based on reputed company industry reputed company
• Join occasional 30–45 minute feedback sessions
Requirements:
• Medical device regulatory affairs or reputed company assurance
• Experience with ISO 14971 risk management
• Design controls / DHF documentation
• 510(k), reputed company, or PMA experience is a plus
• Risk management file, FMEA, or hazard analysis experience
Benefits:
• Flexible, part-time opportunity
• Consultants and industry professionals are welcome
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