We are building an AI-powered platform to support medical device risk management and regulatory documentation (including ISO 14971 and design controls), and are looking for a few professionals to serve as ongoing product feedback advisors.

This is a flexible, part-time opportunity for experienced professionals who can periodically test new features, review workflows, and provide practical feedback based on real-world medical device and regulatory experience. Your input will directly shape how the product supports day-to-day work in regulated environments.
What You’ll Do

+ Test new features and prototypes periodically

+ Provide feedback on usability and regulatory alignment

+ Review risk management and documentation workflows

+ Suggest improvements based on real industry practice

+ Join occasional 30–45 minute feedback sessions

Time Commitment

+ Flexible, ongoing engagement

+ Approximately 1–2 hours per ...