Jobs at BioTalent

Lead Android Software Engineer responsible for designing, developing, and maintaining Android applications for medical devices using Kotlin. Own complex features end-to-end from requirements through implementation, verification, and post-market support, with emphasis on hardware communication via BLE and other protocols.…See more Collaborate with embedded, cloud, systems, quality, and regulatory teams to ensure software reliability in a regulated environment. Requires 7+ years of professional Android development, advanced Kotlin proficiency, strong architecture knowledge, and experience with automated testing and CI/CD workflows.

Staff Quality Engineer for a medical device manufacturer responsible for owning and continuously improving the Quality Management System across the full product lifecycle. The role involves coordinating QMS processes and documentation, leading design control programs, managing change control reviews, directing CAPA activities, handling complaints and supplier qualification, and leading internal audit programs.…See more Requires 8–10+ years of medical device quality experience, 3+ years in quality system auditing, and strong expertise in ISO quality systems and FDA-regulated device standards.

Lead and scale a software organization at a medical-device company from lean team to commercial scale, reporting to VP of R&D. Responsibilities include hiring and mentoring engineers, establishing coding standards and workflows, translating executive vision into technical strategy and roadmaps, staying hands-on with prototyping and code review, and coordinating across hardware, data science, regulatory, and executive functions.…See more Requires 10–15+ years in software development with 5+ years managing technical teams, experience shipping mobile apps and cloud backends for connected devices, regulated-industry background (medical device preferred), and fluency in modern DevOps, CI/CD, and automation testing.

Principal Systems Engineer leading full product development lifecycle for a Class II Medical Device, defining system architecture and engineering strategy across electrical, firmware, software, and manufacturing domains. Owns multidisciplinary systems end-to-end, establishing development processes (CI/CD, automated testing, version control), leading embedded hardware and firmware architectures, and ensuring FDA compliance and Design Controls adherence.…See more Serves as primary technical authority coordinating internal teams and external partners, conducting design/architecture reviews, supporting manufacturing scale-up, and mentoring cross-functional engineers. Requires 12+ years of multidisciplinary product development with demonstrated systems engineering expertise, regulated-industry experience, and technical leadership without direct authority.