Back
Senior, niche medical-device specialization but metro location increases applicant density.
Highly specialized regulated medical-device and hardware-integration skills limit cross-industry transferability.
Explicit 15+ years, regulated medical-device experience, and mandatory technical and compliance skills.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Own end-to-end software development lifecycle for ZEISS refraction and centration medical devices, ensuring high-quality, reliable, and compliant solutions.
Lead and evolve software architecture, integration with hardware, sensors, and optics, maintaining compliance with medical device standards and cybersecurity best practices.
Build and manage a high-performing global engineering team, collaborating across functions to translate clinical and product needs into scalable software solutions.
Bachelor’s or Master’s degree in Computer Science, Software Engineering, Electronics, Biomedical Engineering, or related field.
15+ years of software engineering experience in medical devices, including leadership roles.
Experience in regulated medical technology environments, with strong skills in Windows-based device software development.
Not explicitly mentioned in the JD: Notice period requirement.
Experienced leader capable of managing full device software lifecycle in regulated medical device context.
Strong technical expertise in software-hardware integration, architectural design, and compliance with medical and cybersecurity standards.
Proven track record working with cross-functional and global teams delivering complex medical device software products.