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Aidoc is the market leader in healthcare AI, deploying clinical AI solutions across 2,000+ medical centers worldwide and supporting nearly 50 million patients annually. The company has raised over $500 million since 2016 and holds a record number of FDA-cleared solutions.
This is a unique opportunity to rebuild Aidoc's QA strategy from the ground up for regulated medical device products. You will own the entire testing lifecycle—from defining strategy and designing test architecture to building test environments, writing automation, and executing releases. This is not a maintenance role; you will rethink how the organization tests, define a modern QA vision, and execute it hands-on.
Key responsibilities include:
**QA Strategy & Test Architecture**: Rebuild and own the QA strategy end-to-end for regulated products. Design testing approach, methodology, and best practices across unit, integration, automation, and manual layers. Establish quality gates, release criteria, and acceptance standards.
**Test Environments & Infrastructure**: Define and build new test environments including staging, sandboxes, and test data sets. Select, integrate, and improve testing tools and frameworks (pytest, Playwright, etc.). Drive CI/CD integration of testing across the development pipeline.
**Feature Testing & Planning**: Partner with developers and Regulatory & Compliance on new features from the design phase. Define test scenarios and acceptance criteria. Author Test Strategy Documents aligned with engineering and regulatory needs. Execute manual and automated tests before production releases.
**Test Automation**: Build automated tests using existing infrastructure and extend where needed. Gradually increase automation coverage across all features. Maintain, refactor, and continuously improve automated tests.
**Release & Regulatory Quality**: Define test plans for each release and coordinate V&V activities. Lead configuration, change, and release management per regulatory requirements. Support internal and external audits (ISO 13485, FDA, MDSAP).
You will have full end-to-end ownership of the testing lifecycle for regulated products, working closely with R&D teams and Regulatory & Compliance to ensure products meet both engineering excellence and medical device regulatory standards.
