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SandboxAQ
United States
Source: SandboxAQ careers · View original posting
From SandboxAQ's posting. “We” and “our” refer to the employer.
SandboxAQ is a high-growth company delivering AI solutions that address some of the world's greatest challenges. The company’s Large Quantitative Models (LQMs) power advances in life sciences, financial services, navigation, cybersecurity, and other sectors.
We are a global team that is tech-focused and includes experts in AI, chemistry, cybersecurity, physics, mathematics, medicine, engineering, and other specialties. The company emerged from Alphabet Inc. as an independent, growth capital-backed company in 2022, funded by leading investors and supported by a braintrust of industry leaders.
At SandboxAQ, we’ve cultivated an environment that encourages creativity, collaboration, and impact. By investing deeply in our people, we’re building a thriving, global workforce poised to tackle the world's epic challenges. Join us to advance your career in pursuit of an inspiring mission, in a community of like-minded people who value entrepreneurialism, ownership, and transformative impact.
The Opportunity
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 our fleet of devices in the field running 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.
This is a player-coach role. You will spend meaningful time writing code, reviewing complex PRs, and owning software correctness across interfaces from device to cloud to customer. You lead by doing, setting the standard for code quality and testing. You know what “good” looks like.
Mentor a growing team of senior and staff engineers, fostering a culture of technical excellence, rigorous review, and psychological safety.
Lead the engineering team’s adherence to our quality system, including applicable medical device standards 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 Collaboration
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.
Essential Skills & Experience
7+ years of software engineering experience
, with at least 4 years serving as a Technical Lead or Architect for complex, distributed, and cloud-heavy systems.
Proven experience delivering regulated software in a quality-management system, through the full product lifecycle. In addition to core med-tech, relevant industries include aerospace, automotive, and life sciences.
Expertise at data interfaces
: Proven experience aligning technical requirements and code development across data interfaces / across different SW components.
Mastery in at least one modern systems language: Rust, C++, Go, or Python.
Expertise in cloud (AWS preferred)
: Infrastructure as Code (Terraform), containerization (Docker/Kubernetes) and observability (Cloudwatch/Datadog).
Highly Desired Skills & Experience
Experience designing HIPAA/GDPR-compliant systems, including encryption, audit logging, and secure data transmission.
Proven experience delivering regulated medtech software (IEC 62304 Class B/C) through the full product lifecycle.
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.
Experience with "Software as a Medical Device" (SaMD) products that have successfully scaled in the market.
Hands-on experience integrating software with hospital IT systems (Epic, Cerner) using standards like HL7 or FHIR.
Background in PKI, device authentication, or threat modeling for connected devices.
Familiarity with cardiac diagnostics, ECG workflows, or similar physiological monitoring platforms.
Why Join Us?
We offer a comprehensive and competitive benefits package designed to support your health, financial well-being, and life outside of work.
Compensation
Competitive base salary, performance-based incentives or bonuses (where applicable), and equity participation.
We are committed to fostering a culture of belonging and respect, where diverse perspectives are actively sought and valued. Our multidisciplinary environment provides ample opportunity for continuous growth - working alongside humble, empowered, and ambitious colleagues ready to tackle epic challenges.
Equal Employment Opportunity
: All qualified applicants will receive consideration regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status.
Accommodations
: We provide reasonable accommodations for individuals with disabilities in job application procedures for open roles. If you need such an accommodation, please let a member of our Recruiting team know.
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