Senior Quality Systems Specialist

Overview

Key role in maintaining Quality Management System for digital therapeutics compliance.

Ideal candidate has 3+ years in Quality Management for medical devices and knowledge of relevant regulations.

Locations

• United States

Requirements

• 3+ years in Quality Management
• Knowledge of ISO 13485
• Experience in medical devices

Responsibilities

• Drive design control activities
• Support risk management activities
• Lead quality system processes
• Collaborate on quality management improvements
• Participate in audits
• Resolve quality system issues
• Provide Document Control support

Benefits

• Generous vacation policy
• Professional development fund
• Flexible working arrangements
• Stock options