At Innolitics, we're a growing, collaborative team actively learning how to use Agentic AI tools to produce robust, traceable, high-quality systems where correctness, safety, and documentation matter. Agentic AI tools are changing software engineering. We see this as an opportunity, not a threat.
As an engineer here, you won't just write production code — you'll develop real expertise in medical device regulations, quality systems, verification & validation, and the realities of FDA-facing software.
The role: You'll play a cross-functional role across software development and regulatory projects — building new medical device software using web and mobile technologies while producing technical documentation for FDA clearance. You'll also work with clients who have existing devices, helping them remediate or build out their technical design history files. It's deep technical work paired with strong client communication, all in collaboration with our team of regulatory experts.
What we're looking for:
PhD, Masters, or Bachelors in CS, Biomedical Engineering, or related field 5+ years software engineering experience 3+ years in web technologies 3+ years in mobile development Fluent in TypeScript and Python Fluent in using AI tools as a productivity multiplier Capable of learning new technologies quickly and independently
What we offer:
$130K–$160K + 10% performance bonus Fully remote (U.S. only) Flexible hours Weekly "10x Time" for learning & growth Annual team retreat
If you're excited by the intersection of technology, medicine, and regulation — apply now!
Read more and Apply here: https://innolitics.com/join/senior-web-mobile-medical-device...