
Principal Engineer - Digital Health Products
- London
- Permanent
- Full-time
- Experience leading the technical design, development, and delivery of precision medicine / personalised health software products or devices.
- Knowledge and experience of large scale processing and management of sensitive health data, focused on healthcare delivery and clinical trials.
- Prior experience with Azure (ideally), AWS or GCP.
- Comfortable working with Infrastructure as Code, ideally with knowledge of Terraform.
- Knowledge of good data modelling and design patterns; in-depth knowledge of relational databases (e.g. PostgreSQL) and familiarity other types of data store (blob, document, graph).
- Experience in a technical leadership role in a modern, agile development team, leading the adoption of practices like code review, TDD, CI/CD and pairing using tools like Git and GitHub.
- Experience of operationally managing software components once live, including; observability, logging, metrics, error reporting, debugging and live incident management.
- Experience working in/with cross-functional teams consisting of engineers, product, UX and non-technical stakeholders.
- Experience leading the work of multiple cross-functional teams to deliver an overall objective.
- Comfortable in facilitating complex technical discussions with organisation-wide impact, encouraging collaboration and providing direction.
- Proven ability to communicate with stakeholders and audiences at different levels, including exec level (CTO, CPO, etc).
- Proven experience developing Software as a Medical Device (SaMD) in compliance with the UK MDR 2002 and applicable international standards (ISO 14971, ISO 13485, IEC 62304, IEC 62366…):
- Demonstrated ability to produce and maintain required software lifecycle documentation required under IEC 62304 including software development plans, architecture and design specifications, unit/integration/system test protocols and reports, software requirements traceability matrices, anomaly/change records etc.
- Hands-on knowledge of quality management systems (ISO 13485), including participation in internal audits, CAPA processes, and ensuring software lifecycle documentation is inspection-ready for regulatory review.
- Strong understanding of risk management per ISO 14971, and usability engineering principles per IEC 62366.
- Familiarity with clinical safety and health software standards relevant in the UK (e.g. DCB0129/0160) and the associated regulatory expectations for safe deployment of clinical software.
- Experience of of supporting regulatory submissions (Technical Files, Design Dossiers, or equivalent), including responding to regulator/Approved Body queries on software documentation.
- Experience working in small, growing organisations with a high degree of ambiguity, where flexibility is valued.
- Expert understanding of software quality and experience leading quality improvement initiatives across multiple cross-functional teams.
- A track record of successfully mentoring both highly experienced and early career engineers.
- Generous Pension Scheme – We invest in your future with employer contributions of up to 12%.
- 30 Days Holiday + Bank Holidays – Enjoy a generous holiday allowance with the flexibility to take bank holidays when it suits you.
- Enhanced Parental Leave – Supporting you during life’s biggest moments.
- Cycle to Work Scheme – Save 25-39% on a new bike and accessories through salary sacrifice.
- Home & Tech Savings – Get up to 8% off on IKEA and Currys products, spreading the cost over 12 months through salary sacrifice
- £1,000 Employee Referral Bonus – Know someone amazing? Get rewarded for bringing them on board!
- Wellbeing Support – Access to Mental Health First Aiders, plus 24/7 online GP services and an Employee Assistance Programme for you and your family.
- A Great Place to Work – We have a lovely Central London office in Holborn, and offer flexible and remote working arrangements.
We are sorry but this recruiter does not accept applications from abroad.