Senior Embedded Software Engineer

Ko2 Embedded Recruitment Solutions Ltd — United Kingdom · Posted ~5 hours ago

Senior Full-time Hybrid £60000-£70000 + 8% bonus

Skills

Embedded software development Software architecture Software development standards Software quality assurance Technical documentation Regulatory compliance Cross-functional engineering C++ Embedded software

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Summary ✨ AI‑Generated

A medical technology organization is seeking a Senior Embedded Software Engineer to take ownership of embedded software across its engineering activities. You will define architecture, establish development standards, ensure software quality and documentation, and support compliance with stringent safety and regulatory requirements. The role involves close collaboration with hardware, systems, verification, and regulatory specialists on reliable technology used in demanding clinical environments. Flexible hybrid working and a competitive salary with bonus are offered.

Highlights

High-impact senior engineering role with ownership of embedded software strategy, architecture, development standards, quality, documentation, and regulatory compliance. Flexible hybrid working and a performance bonus are offered, with the opportunity to work on safety-critical technology used in clinical environments.

Description

Senior Embedded Software Engineer Location: Runcorn, with flexible hybrid working from home Salary: £60,000 – £70,000 DOE, plus 8% bonus About the company Our client is an innovative medical technology business. They develop critical point-of-care devices for GP surgeries, intensive care units and specialist hospital departments. In these settings, performance, safety and reliability can't be compromised. Their products help clinicians, extend lives, and are built to work reliably in demanding clinical environments. The opportunity As Senior Embedded Software Engineer, you'll own embedded software development across the business and be its software authority. You'll define the software architecture, set development standards, and make sure software quality, documentation and regulatory compliance meet medical-grade requirements. You'll work closely with the hardware, systems, verification and regulatory teams on products used in hospitals, critical care wards and frontline clinical settings. This is a key role in a growing medical device company, and your decisions will directly affect both product performance and patient outcomes. Technical skills profile Extensive experience in several programming languages, including C, C++ and PythonDeep experience developing bare-metal and RTOS firmware for memory-constrained microcontrollersStrong knowledge of networking protocols and principles, especially as they apply to cloud computingProven experience developing wireless communication and remote monitoring systemsAdvanced skills in engineering simulation and calculationConfident using common engineering tools for design (CAD, schematics, PCB layout), simulation, prototyping and measurement Regulated-industry experience You must have experience in medical devices or another regulated industry. We're looking for hands-on experience developing software in a regulated environment. Medical devices is ideal, but we'll also consider experience from other safety-critical sectors. You'll need: Proven experience developing embedded software for medical devices or another regulated industry, such as aerospace or automotive safetyWorking knowledge of relevant standards and regulatory frameworks, such as ISO 13485, IEC 62304 and IEC 60601, or equivalentsA strong understanding of the documentation, traceability and verification required for safety-critical softwareExperience working with regulatory, quality or verification teams throughout the software development lifecycleThe technical credibility to define architecture and set development standards at a senior level If you come from another safety-critical or regulated sector and want to specialise in medical technology, we'd welcome your application. You'll need to show real experience of regulated development practices. Why apply? This is a rare chance to combine advanced embedded software engineering with real clinical impact. You'll join an ambitious, committed team focused on improving patient outcomes through good engineering. Your regulated-industry expertise will be central to the products you help build. To apply, send your up-to-date CV and a cover letter to KO2 Embedded Recruitment Solutions.