Regulatory Affairs Software Quality Engineer

Overview

Experienced Regulatory Affairs Software Quality Engineer supporting tool development and validation.

Ideal candidate has 4+ years of experience in regulatory affairs and strong programming skills.

Locations

• United States

Requirements

• 4+ years experience required
• Experience in Medical Device Product Development
• Ability to program in Python, JavaScript, C#

Responsibilities

• Support Regulatory and Quality teams
• Develop and validate tools
• Analyze data
• Generate test cases
• Develop software tools
• Monitor patient data for errors
• Work productively in a remote environment

Benefits

• Medical, dental, vision care
• 401(k) with employer match
• Self-managed PTO
• Generous parental leave
• Virtual events
• Yearly retreats
• Collaborative work environment