Job Summary
A company is looking for a Regulatory Affairs Software Quality Engineer.
Key Responsibilities
- Validate 3rd party and internally developed tools
- Create custom tools for internal use and automate data collection and reporting
- Update software and cyber-related documentation for agency submissions
Required Qualifications
- Bachelor's degree with 4+ years of experience or Master's degree with 2+ years of experience in related roles
- Experience with Non-Product Software Tool Validation
- Ability to develop software tools using programming languages such as Python, JavaScript, or C#
- Familiarity with global medical device regulations and experience in data analysis
- Demonstrated ability to work productively in a remote environment
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