Principal Software Engineer, Medical Devices

🕒 May 27

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SandboxAQ

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2021

🤖 Artificial Intelligence

🔒 Cybersecurity

💊 Pharmaceuticals

Artificial Intelligence • Cybersecurity • Pharmaceuticals

SandboxAQ is a company developing quantitative AI and quantum-inspired technologies to solve real-world problems across drug discovery, materials science, cybersecurity, and navigation. They build large quantitative models (LQMs) grounded in physics and chemistry to predict molecular properties, accelerate therapeutic design, and simulate complex chemical and catalytic processes, while also applying their expertise in AI and post-quantum cryptography to enhance digital security and navigation in GPS-denied environments.

📋 Description

• 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).

🎯 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).

🏖️ Benefits

• Comprehensive medical, dental, and vision coverage for employees and dependents with generous employer premium contributions • Retirement savings with company matching • Paid parental leave • Inclusive family-building benefits • Flexible paid time off • Company-wide seasonal breaks • 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