Senior Staff Software Engineer, Medical Devices

SandboxAQ

16d • $208,000 - $390,000

About The Position

AQMed is developing a next-generation, non-invasive cardiac diagnostic platform designed to revolutionize how heart health is assessed. The team operates at the intersection of regulated medical device development and fast-paced startup innovation, with a strong emphasis on quality, scientific rigor, and patient safety. We are seeking a Senior Staff Software Engineer to serve as the Technical Lead for our medical device software platform. In this role, you will own the software architecture that powers our device—from embedded Linux to the cloud. Your architectural decisions will keep the platform safe, maintainable, and extensible as our product evolves. You will be raising engineering standards and architecture quality, serving as the final technical authority for our regulated medical product.

Requirements

• 10+ years of software engineering experience, with at least 4 years serving as a Technical Lead or Architect for complex, distributed, and cloud-heavy systems.
• Medical Device Experience: Proven experience delivering regulated software (IEC 62304 Class B/C) through the full product lifecycle.
• Full-Stack Technical Mastery: Proficiency in modern systems languages (Rust, C++, or Go) and Python. Deep expertise in cloud infrastructure (AWS/GCP), Infrastructure as Code (Terraform), containerization (Docker/Kubernetes) and observability (Cloudwatch/Datadog).

Nice To Haves

• Security & Data Privacy: Experience designing HIPAA/GDPR-compliant systems, including encryption, audit logging, and secure data transmission.
• Product-Aware Mindset: Demonstrated ability to make architectural trade-offs that favor long-term product flexibility and user experience. You can give examples of how you designed a system to accommodate future business needs that weren't yet fully defined.
• SaMD Commercialization: Experience with "Software as a Medical Device" (SaMD) products that have successfully scaled in the market.
• EHR/EMR Integration: Hands-on experience integrating software with hospital IT systems (Epic, Cerner) using standards like HL7 or FHIR.
• Cybersecurity Expertise: Background in PKI, device authentication, or threat modeling for connected devices.
• Cardiology Domain Knowledge: Familiarity with cardiac diagnostics, ECG workflows, or similar physiological monitoring platforms.

Responsibilities

• Own the Platform Architecture: Serve as the final technical authority for the end-to-end software stack, spanning embedded firmware, in-field Linux devices, cloud data pipelines (AWS/GCP), and the clinician-facing web application.
• Product-Ready Foundation: Design clear and flexible interfaces such that our platform can evolve with our product roadmap without major refactors.
• Data Path Integrity: Design and maintain a HIPAA-compliant, production-grade data platform that ensures data confidentiality, integrity, and availability from the sensor to the cloud.
• Hands-on Engineering: This is a player-coach role. You will write code, review complex PRs, debug hardware-software integration issues in the lab, and configure CI/CD pipelines. You lead by doing, setting the standard for code quality and testing. You know what “good” looks like.
• Technical Mentorship: Mentor a growing team of senior and staff engineers, fostering a culture of technical excellence, rigorous review, and psychological safety.
• Drive Quality & Compliance: Lead the engineering team’s adherence to applicable medical device standards (e.g. IEC 62304, ISO 14971) and regulations. You are the gatekeeper ensuring that design outputs (code) meet design inputs (requirements) and that our "move fast" culture never compromises patient safety and critical product functions. Scale strong engineering practices across the team, including design reviews, code review quality, test strategy and technical documentation.
• Cross-functional execution: Partner with Product, Clinical and Regulatory stakeholders to translate product requirements, clinical performance goals and regulatory inputs into concrete, actionable technical plans, engineering specifications and development timelines. Ensure that our software architecture, implementation and documentation support our clinical study needs and regulatory plans (e.g. 510(k) and De Novo).

Benefits

• Competitive base salary, performance-based incentives or bonuses (where applicable), and equity participation.
• Comprehensive medical, dental, and vision coverage for employees and dependents with generous employer premium contributions, retirement savings with company matching, paid parental leave, and inclusive family-building benefits.
• Flexible paid time off, company-wide seasonal breaks, and support for flexible work arrangements that enable sustainable performance.
• Opportunities for continuous learning and growth through on-the-job development, cross-functional collaboration, and access to internal learning and development programs.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: No Education Listed