Software Design Control Engineer

About the role

Company Overview

Echo Neurotechnologies is an exciting new startup in the Brain-Computer Interface (BCI) space, driving innovation through advanced hardware engineering and AI solutions. Our mission is to deliver cutting-edge technologies that restore autonomy to people living with disabilities and improve their quality of life.

Team Culture

Join a small, dedicated team of knowledgeable and motivated professionals. Our early-stage environment offers the opportunity to take ownership of broad decisions with significant and long-lasting impact. We emphasize continuous learning and growth, fostering cross-functional collaboration where your contributions are vital to our success.

Job Description

We are seeking a Software Design Control Engineer to drive end-to-end documentation and process rigor across our Class III medical device software products, supporting both clinical trials and commercialization. This role sits at the intersection of software engineering, quality systems, and regulatory compliance. You will bring medical device best practices across quality and engineering to ensure our software is safe, effective, compliant, and ready for market.

Role Responsibilities

- Embedded Design Controls: Work alongside software engineers to author, review, and maintain comprehensive design control documentation, including Software Requirements Specifications, Architecture & Design Documents, and Traceability Matrices.

- Lifecycle Compliance: Ensure software development processes align with IEC 62304 (Medical Device Software Lifecycle), ISO 13485, and FDA 21 CFR Part 820 regulations.

- Risk Management: Author and maintain software risk management files, including Software FMEAs per ISO 14971.

- V&V Partnership: Produce software verification and validation (V&V) protocols and reports in coordination with the engineering and test teams to ensure full traceability.

- Regulatory Submission Prep: Compile and organize necessary software technical documentation for regulatory submissions.

- Post-Market Support: Maintain and update software documentation for post-market surveillance, CAPAs, and software updates.

Qualifications

Required Qualifications

- Experience: 10+ years of experience in the medical device industry, specifically working with software-driven or connected medical devices (Class II or Class III).

- Standards Expertise: Deep familiarity with IEC 62304, ISO 14971, and FDA Software Validation Guidelines, with hands-on design-control experience applying these through at least one full software lifecycle from requirements to FDA submission and clearance.

- Technical Background: A Bachelor’s degree in Computer Science, Biomedical Engineering, Software Engineering, or a related field, or equivalent practical engineering experience, resulting in strong technical skills to read code and architecture, align technical scope with engineers, and ensure consistency across documents.