Senior Associate, Regulatory Affairs- Human Factors

Overview

Role involves supporting regulatory and human factors engineering initiatives for medical devices.

Ideal candidate should have experience in medical device development and usability engineering.

Locations

• United States

Requirements

• Bachelor's degree in scientific, engineering, or regulatory discipline
• Experience with medical device development required
• Experience with medical device usability engineering preferred

Responsibilities

• Draft usability engineering files
• Conduct use-related risk analysis
• Design usability studies
• Develop regulatory services for clients
• Communicate with regulatory bodies
• Collaborate with other departments
• Complete other assigned projects