RA/QA Specialist

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 support 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.

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:

• Risk Management Ownership (60%)
  • Lead ISO 14971‑compliant risk files for all active product versions.
  • Drive risk updates for every release and patch.
  • Ensure traceability between hazards, requirements, risk controls and verification evidence.
  • Help configure Jira for structured risk traceability.
  • Align risk documents with clinical evaluations, field safety feedback and PMS signals.
  • Assist in closing Notified Body non‑conformities related to risk.
• Technical Documentation & Release Review (30%)
  • Review and update Technical Documentation for every release cycle.
  • Ensure consistency across the IFU, risk files and intended purpose.
  • Support preparation for Notified Body audits and ongoing surveillance.
  • Participate in internal design reviews from a compliance perspective.
• Cross‑Functional Support (10%)
  • Work with developers to ensure risk controls are correctly implemented.
  • Provide input into documentation to align with IEC 62304.
  • Help optimise traceability systems and documentation tools.

What We’re Looking For:

• 3–6 years of experience in Medical Device or SaMD within a QA or RA/QA engineering capacity.
• Deep knowledge of ISO 14971 and EU MDR requirements.
• A hands‑on executor who enjoys working at the intersection of technical engineering and regulatory standards.

How We Work:

We empower everyone at Doccla to take ownership of their work and the company’s mission. We act ethically and always put patient safety and outcomes first. To thrive here, you’ll need a can‑do attitude, an action‑oriented approach and a willingness to learn and grow through open feedback. We’re a hybrid team, with offices in London, Denmark, Germany and Stockholm. Most of our team is London‑based and enjoys in‑person time at our WeWork HQ 1–3 days per week, where you’ll find great lunch, barista coffee and a pet‑friendly space. Some roles are fully remote, depending on the team and responsibilities.

What You’ll Get:

• Annual Leave & Holidays: 25 days annual leave + up to 8 UK bank holidays. Option to buy or sell holidays.
• Remote Working: Flexible remote options.
• Financial Benefits: Employee stock options. 4% pension on full basic pay. 4× salary life insurance.
• Health & Wellness: Private health insurance. 4 months full pay for birthing parent. 4 weeks full pay for non‑birthing parent. Sick pay.
• In‑Office Perks (London HQ): Free daily lunch. Pet‑friendly office.
• Other Benefits: £500 L&D budget per person. Cycle to work scheme.

In Return for Your Hard Work:

A competitive compensation package (base + stock options) with half‑year and annual performance reviews. The chance to work on patient‑first, system‑level healthcare challenges in one of Europe’s leading health‑tech companies. Opportunities for growth and leadership; we want you to challenge the status quo, own your impact and continue developing, with our full support.

Diversity at Doccla:

We embrace diversity. To build a great product, we need a team with a wide range of perspectives, backgrounds, and experiences. We’re committed to equal opportunity hiring regardless of race, religion, gender identity, sexual orientation, age, disability or background. If you’re excited about the role, we encourage you to apply even if your experience doesn’t match every point.

Safer Recruitment:

We are committed to safer recruitment practices. As Doccla is a CQC registered company, a Disclosure and Barring Service check will be required for all roles. It is an offence to apply for such work if you are barred from working with children or vulnerable adults.