Documentation & Quality Associate (Junior) Lisboa

Documentation & Quality Associate (Junior)
Lisboa
Lisboa, Lisboa, Portugal

About Us:

At Blood
Flow, we are developing the future of automated clinical workflows by leveraging AI to provide deep, contextual interpretation of blood test results. Our platform combines
- edge large language models,
- augmented generation (RAG), and structured medical reasoning to transform raw laboratory data into actionable, clinically relevant insights.

We focus on building scalable and secure AI systems that integrate seamlessly with healthcare environments, including cloud and
- premise deployments within hospitals. Our technology bridges complex medical data with advanced natural language understanding to support clinicians in making faster and more informed decisions.

If you are passionate about AI, healthcare technology, and building robust systems that operate under strict regulatory and security requirements, Blood
Flow offers a unique opportunity to innovate at the intersection of medicine and artificial intelligence.

Role Summary:

We're hiring a junior documentation and quality associate to support the Head of Quality & Regulatory in writing, organizing, and managing our regulatory and quality documentation. You’ll help maintain traceability, ensure we’re always
- ready, and assist in our path toward key certifications.

You’ll work directly on documentation required for:

• ISO 13485
• ISO 27001
• ISO 27701
• CE / MDR

Responsibilities:

• Draft and organize SOPs, policies, and regulatory documentation
• Support creation of technical files for medical software certification
• Maintain version control and document traceability
• Assist in preparing for internal and external audits
• Collaborate with the tech team to collect and archive quality records

What we’re looking for:

• 2 years experience in documentation, QA, or compliance
• Excellent writing skills and attention to detail
• Familiarity with Notion, Confluence, Git, or other documentation tools
• Interest in regulatory affairs and medtech compliance
• Highly organized and proactive

How to apply:

Send your CV or Linked
In to