At a Glance
- Tasks: Ensure compliance and risk management for our innovative medical software solutions.
- Company: Join Doccla, a pioneering company in Virtual Care and Remote Monitoring.
- Benefits: Enjoy competitive salary, 25 days annual leave, and a flexible hybrid work environment.
- Other info: Collaborative culture with opportunities for growth and learning.
- Why this job: Be part of a mission-driven team making a real impact in healthcare.
- Qualifications: 3-6 years in Medical Device QA/RA with knowledge of ISO 14971 and EU MDR.
The predicted salary is between 40000 - 50000 £ per year.
A Bit About Us
We’re Doccla, and we’re redefining where and how healthcare is delivered. Our Virtual Ward and Remote Monitoring Solutions enable hospitals and health systems to care for patients at home. We support patients across the full care journey from early discharge and acute recovery to long‑term condition management and proactive care. We provide everything clinicians need to deliver safe, effective Virtual Care: medical‑grade devices, logistics, patient onboarding, EHR integration, and an end‑to‑end clinical platform built around real‑world workflows. We currently work with over 60% of NHS ICBs and supporting health systems across the UK, Ireland, France, and the DACH region to reduce hospital pressure, improve outcomes, and create a more resilient model of care. We’re backed by top European investors, having secured £35m in Series B funding led by Lakestar, with participation from Elaia, General Catalyst, Speedinvest, and Bertelsmann.
Why Join Us?
This is your chance to join Doccla at a key stage in our growth. We’re building the category leader in Virtual Care and Remote Patient Monitoring. You’ll be part of a highly entrepreneurial, mission‑driven team that combines expertise across clinical, technical, commercial, and operational domains. We’re solving real problems for patients and health systems and growing fast.
What You’ll Do as a RA/QA Specialist
As our RA/QA Specialist, you are the vital link between Engineering and Compliance. You will own the risk management and technical documentation for the Doccla SaMD (Software as a Medical Device) platform. This is an execution‑focused role where you’ll ensure our product lifecycle is audit‑ready, MDR‑compliant, and built on a defensible risk framework.
What Experience You’ll Bring to the Team
- Risk Management Ownership (60%)
- Maintain Standards: Lead ISO 14971‑compliant risk files for all active product versions.
- Release Management: Drive risk updates for every release and patch.
- Ensure Traceability: Connect the dots between Hazards, Requirements, Risk Controls, and Verification evidence.
- Tooling Support: Help configure Jira for structured risk traceability.
- Feedback Loop: Align risk docs with clinical evaluations, field safety feedback, and PMS signals.
- Audit Support: Assist in closing Notified Body non‑conformities related to risk.
- Technical Documentation & Release Review (30%)
- Technical Integrity: Review and update Technical Documentation (TD) for every release cycle.
- Accuracy Check: Ensure consistency across the IFU (Instructions for Use), risk files, and intended purpose.
- Audit Prep: Support preparation for Notified Body audits and ongoing surveillance.
- Design Reviews: Participate in internal design reviews from a compliance perspective.
- Cross‑Functional Support (10%)
- Engineering Partnership: Work with developers to ensure risk controls are correctly implemented.
- Software Lifecycle: Provide input into documentation to ensure alignment with IEC 62304.
- Process Improvement: Help optimise our traceability systems and documentation tools.
What We’re Looking For
- Experience: 3–6 years in Medical Device or SaMD (Software as a Medical Device) within a QA or RA/QA Engineering capacity.
- The
RA/QA Specialist in London employer: Doccla UK Limited
At Doccla, we are not just redefining healthcare delivery; we are creating a vibrant and supportive work environment that empowers our employees to make a real impact. As a RA/QA Specialist, you will join a mission-driven team in London, where collaboration and innovation thrive, alongside opportunities for professional growth and development. Enjoy a hybrid work model with access to our modern WeWork HQ, fostering a culture of flexibility, creativity, and a strong commitment to patient safety.
StudySmarter Expert Advice🤫
We think this is how you could land RA/QA Specialist in London
✨Tip Number 1
Network like a pro! Reach out to people in the healthcare and tech sectors, especially those who work at Doccla or similar companies. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for interviews by diving deep into Doccla's mission and values. Show us that you’re not just another candidate; you’re someone who genuinely cares about redefining healthcare delivery and improving patient outcomes.
✨Tip Number 3
Practice your STAR technique for answering behavioural questions. We want to hear about specific situations where you've demonstrated your skills in risk management or compliance. Make it relatable and relevant to the RA/QA role!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows us you’re serious about joining our mission-driven team.
We think you need these skills to ace RA/QA Specialist in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the RA/QA Specialist role. Highlight your experience with ISO 14971 and EU MDR requirements, as well as any relevant projects you've worked on. We want to see how your skills align with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about virtual care and how your background makes you a perfect fit for Doccla. Keep it concise but impactful – we love a good story!
Showcase Your Hands-On Experience:In your application, be sure to highlight any hands-on experience you've had in risk management or technical documentation. We’re looking for someone who can hit the ground running, so let us know how you've tackled similar challenges before.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us that you’re genuinely interested in joining our mission-driven team!
How to prepare for a job interview at Doccla UK Limited
✨Know Your Regulations
Familiarise yourself with ISO 14971 and EU MDR requirements before the interview. Being able to discuss these regulations confidently will show that you understand the compliance landscape and can effectively contribute to Doccla's mission.
✨Showcase Your Experience
Prepare specific examples from your past roles where you've successfully managed risk files or contributed to technical documentation. Highlighting your hands-on experience will demonstrate your capability as an RA/QA Specialist.
✨Understand the Product Lifecycle
Brush up on the software lifecycle and how it relates to risk management. Be ready to discuss how you would ensure audit readiness and compliance throughout the product lifecycle, as this is crucial for the role.
✨Ask Insightful Questions
Prepare thoughtful questions about Doccla's approach to remote monitoring solutions and how they integrate risk management into their processes. This shows your genuine interest in the company and helps you assess if it's the right fit for you.
