Lumisonix Medical is building a medical device solution for chronic wound care (Diabetic Foot Ulcers). We’re a small, fast-moving team working with partners across Europe - and we’re looking for a Biomedical Engineer who wants real ownership: build the product, run the plan, coordinate partners, and grow into technical leadership.

You’ll be close to the tech, the clinicians, and the partner teams—turning work packages into real prototypes and clinical progress.

What you’ll do

- **Drive product development execution**
: translate user/clinical needs into requirements, prototypes, tests, and iterations.
- **Coordinate grant project work packages & partners**
 (EU/national style): track deliverables, milestones, dependencies, and keep everyone moving.
- **Run the weekly cadence**
: standups with partners, action tracking, risk/issue log, decision log, and follow-ups.
- **Own documentation discipline**
: meeting notes, technical decisions, basic traceability, prototype build records, V&V planning inputs.
- **Interface with clinical stakeholders**
: support study planning tasks, vendor/site coordination, and make sure timelines match reality.
- **Keep the integrated plan together**
 across hardware/software/AI, verification/validation, and clinical activities.
- **Be hands-on**
: lab work, bench testing, early prototypes—whatever moves the project forward.

Who you are

- **Biomedical engineering background**
 (BSc/MSc) or equivalent with strong practical engineering instincts.
- **0–4 years experience**
 (industry, research, startup, or “serious side projects” all count).
- You’ve actually built things: prototypes, test rigs, firmware/software scripts, data pipelines, lab validation—anything tangible.
- You’re organized enough to run coordination across multiple stakeholders 
**without becoming bureaucratic**
.
- You communicate clearly in English and can lead meetings even if you’re the youngest in the room.
- You’re comfortable with ambiguity and can turn “we need this to work” into a plan by Friday.

Great if you have

- Exposure to 
**medical device development**
 (ISO 13485 mindset, design controls, risk management basics).
- Any experience with 
**grant-funded projects**
 (Horizon/Eurostars/EIC/Innovate UK/Vinnova/etc.) or structured reporting.
- Understanding of 
**EU MDR**
 basics, verification/validation, or clinical study operations.
- Comfort with data/AI or software-heavy products.