CriTech Research, Inc. provides software engineering services for the FDA-regulated medical device industry. ● Specializing in development and validation of safety critical software for medical devices ● Providing software verification and validation as required by the FDA and EU for software – Unit, Integration, and Software System Testing ● Experts at assisting companies to remediate gaps in their software design history file, including reverse engineering of requirements and design, through software safety and performing software verification and validation ● Proven process, strong management, and an exceptional track record with extensive experience in a variety of domains and systems ● 100%, first-time approval record with both the FDA and EU for the over 400 devices we have worked on ● ISO 13485 certified ● We are hiring software engineers with medical device experience. See our website for details. ─ PC Development (Windows, Embedded Windows, C, C++, C#, SQL) ─ Graphical User Interface (GUI) ─ Embedded Microcontrollers ─ Database ─ Mobile Device Development and Test - iOS (Objective C) and Android Platforms (Java) Test Systems – LabVIEW