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Regulatory
MDR Documentation Specialist
Lead and develop technical documentation for our blood collection device.
We are a Polish medtech startup with a young, dynamic and ambitious team. We are developing a blood collection device and looking for someone to lead and develop our technical documentation as the product evolves.
What you’ll do
- Lead and develop technical documentation for our blood collection device
- Own documentation structure and quality across the product development lifecycle
- Collaborate with engineering teams and external advisors
- Ensure document consistency, completeness and ongoing alignment with project needs
Who we’re looking for
- Experience creating and maintaining clear, structured technical documentation
- Someone who can independently own this area end to end
- Strong organisation and attention to detail
- Ability to translate complex information into precise, usable documents
What we offer
- Terms of cooperation tailored individually to scope and commitment
- Hybrid or fully remote work
- Flexible arrangement – it doesn’t have to be full-time from day one
- Full ownership of a critical area and meaningful impact on the product
If you’re looking for new opportunities but not ready to commit full-time right away, we can start with a collaboration and see how it goes. Terms are open for discussion.
Reach out at contact@oreihealth.com with a short introduction.
