Software Safety Engineer

1 мес. назад

75k–85k GBP / yearUnited KingdomEuropeMiddleOnsite

software assessmentregulatory compliance

Software Safety Engineer for medical device software assessment and certification.

Требования

You’ve got a degree in computer science or related discipline
You’ve spent 4+ years in medical device (or other safety critical product) manufacturing, auditing or research, including 2+ years of safety-critical software development experience
You have practical experience with software development fundamentals, including software development life-cycle processes, software verification and validation testing, software configuration management and cybersecurity
You like going down rabbit holes, understanding deeply how things work, and challenging the status quo
You have exceptional written & verbal communication skills
You have worked in different environments and like operating with autonomy on sometimes ambiguous tasks

Как откликнуться

Intro chat with Hann - 30 mins
Interview with Sandy and a member of Devices - 30 mins each
Technical task & interview with Hann - 1 hour
Culture and values interview with James and Jamie - 30 mins each
Referencing & offer

Другое

Authorised by governments around the world to assess medical AI, we remove unnecessary delays from every regulatory approval we do so patients get devices from the future, today. We are proud to count the world’s most ambitious companies building medical technology as customers. You will be joining a team with product-market fit, flowing data, and exponentially growing revenue.
’s Devices function is a team of clinicians, AI experts, and software engineers, working together to assess and certify the most innovative and impactful medical device software.
We pride ourselves on delivering fast and efficient assessments to enable market access, new device updates and ongoing surveillance of a growing portfolio of medical devices.
As we continue to scale our activities and certify more and more medical devices, we need software expertise to provide support across all stages of the customer journey.
You’ll join a team of software experts, conducting swift and accurate device assessments, whilst providing knowledge and expertise to internal functions and external stakeholders.
Get authorised to assess the software lifecycle processes of the most innovative medical devices in the world
Create content to help explain complex regulatory topics to customers and prospects
Screen and action regulatory insights from the latest research, standards and guidance
Support the Sales and Customer Experience function by providing regulatory insights on prospects and customers
Collaborate with our Product, Engineering, and ML teams to optimise our processes and continue to scale them
Support the Technical Operations function as they expand ’s approvals in various jurisdictions and technologies
Guidance knowledge - You have knowledge or training in the relevant standards and guidance relevant for medical device software (e.g. IEC 62304, IEC 81001-5-1)
AI fluent - You have strong technical knowledge of modern generative AI (e.g., LLMs, embeddings, RAG, fine-tuning, evaluation/monitoring) and have a rich understanding of how these systems work - and where they fail