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Own and guide embedded firmware development for next-generation wearable neurostimulation medical devices. Responsibilities include reviewing an external development partner’s work, shaping firmware architecture, ensuring compliance with medical device standards, and contributing hands-on to development, debugging, testing, verification, and documentation. The role will also help establish an internal firmware capability and collaborate with electronics, software, quality, and regulatory teams.

Own and guide firmware development for current and next-generation wearable neurostimulation devices. Responsibilities include reviewing an external development partner’s work, influencing firmware architecture, ensuring compliance with medical-device standards such as IEC 62304, and contributing hands-on to development, debugging, testing, documentation, and problem-solving. The role will also help establish an in-house firmware capability and collaborate with electronics, software, quality, and regulatory teams.

Speculative application for Neupulse’s talent pool. Applicants submit their details for consideration against future vacancies aligned with their skills, experience, and company values. Applications are retained in the recruitment database and reviewed when suitable roles arise. Neupulse does not offer visa sponsorship and requires applicants to have full, unrestricted UK work authorization.

Owns sustaining engineering for wearable neurostimulation devices after launch. Responsibilities include investigating field and production issues, performing root-cause analysis, improving yield and reliability, managing engineering changes and component obsolescence, supporting post-market surveillance, and coordinating with contract manufacturers and suppliers under medical-device quality and regulatory requirements.

Own the transition of wearable neurostimulation devices from validated design to reliable, high-volume production. Responsibilities include NPI, design-for-manufacturing reviews, automated test system development, manufacturing and validation processes, assembly methods, work instructions, supplier and contract manufacturer collaboration, troubleshooting, continuous improvement, and compliance with medical device regulations and quality systems.