WAn innovative medical technology company is seeking a Software Engineer to support the development and continuous improvement of regulated medical device software and associated digital infrastructure
.
Reporting directly to the CTO, this individual will contribute across the full software lifecycle, working closely with hardware, data, regulatory and quality teams to deliver reliable, secure and compliant medical application
s.
The R
oleThe Software Engineer will be responsible for gathering requirements, defining system functionality and developing high-quality, testable software. The role will also support software architecture, cloud infrastructure, verification, cybersecurity testing and the preparation of technical documentation required within a regulated medical device environme
nt.
Key Responsibili
tiesDevelop, test and maintain medical device software across the full development lifecy
cle.Contribute to software architecture and communication between user interfaces, backend systems and algorithmic modu
les.Develop well-designed and efficient software using technologies including C#, .NET, C++, MATLAB and WPF/X
AML.Support the integration of signal-processing, algorithmic and MATLAB-derived modu
les.Build and maintain cloud infrastructure using AWS or similar platfo
rms.Conduct unit, integration, regression and software verification test
ing.Support automated testing, static code analysis, code coverage and CI/CD proces
ses.Prepare test protocols, datasets, expected results and verification repo
rts.Maintain traceability between requirements, risks, design, code, tests, defects and software relea




ses.Investigate and resolve software defects and verification deviati
ons.Maintain Git repositories, branching strategies, pull requests, tags, releases and code review workfl
ows.Prepare and maintain software lifecycle and technical documentation, including architecture, design, traceability, risk management and verification reco
rds.Support software cybersecurity and data-protection activit
ies.Analyse system performance, including sensitivity, specificity and output consiste
ncy.Coordinate software changes, technical impact assessments and controlled relea
ses.Collaborate with external software development or testing providers where requi
red.Ensure development activities comply with applicable quality and regulatory requireme
nts.
Candidate Pr
ofileDegree in Computer Science, Computer Engineering, Telecommunications Engineering or a related technical discip
line.At least two years’ experience in software development and testing, ideally within a medical device or similarly regulated environ
ment.Strong programming knowledge across C#, .NET, C++, MATLAB or comparable technolo
XAML.Practical knowledge of Git-based version control and software release proce
sses.Experience building cloud infrastructure using AWS or a similar plat
form.Understanding of software verification, validation and traceabi
lity.Knowledge of regulated software standards such as IEC 62304, EU MDR, MDCG guidance and FDA requirem
ents.Understanding of cybersecurity and data-protection frameworks, including GDPR, NIS2 and H
IPAA.Embedded software experience would be advantag
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