Join Us in Catalyzing Brain Health Therapy with Real-World Data

At UNEEG Medical, we are on a clear mission: improve epilepsy care and ultimately enhance patients’ quality of life through objective, real‑world EEG data. Our sub‑scalp EEG solution enables remote monitoring of brain activity and is already making an impact across Europe and the US. We are entrepreneurial and ambitious - with the agility of a small company and the discipline of a certified MedTech organization.

The role:

We are seeking a skilled Software Verification Specialist/Software Tester to own the verification strategy and lead the testing of UNEEG’s software applications across the full product lifecycle - from development to post‑market support.

In this role, you will plan, coordinate, execute, and document software testing activities to ensure the quality, safety, and compliance of medical device software. You will collaborate closely with Software Development, Regulatory & Quality, Clinical & Market, and AI & Data Science teams to secure a robust and compliant verification process for all software releases.

Your core responsibilities:

 Verification Strategy Ownership & Technical Execution

• Take full ownership of UNEEG’s software verification strategy and ensure it is continuously maintained and improved

• Continuously optimize the software verification strategy to balance efficiency and thoroughness

• Select and apply suitable test methodologies (functional, integration, regression)

• Establish and maintain test plans, test cases, and test protocols in alignment with ISO 13485 and IEC 62304

• Drive, coordinate, and execute verification activities for software releases

• Log, update, and close issues in the bug/issue tracking system

Documentation & Compliance

• Ensure compliance with UNEEG’s QMS processes and regulatory requirements

• Lead and execute change processes to maintain compliant documentation

• Update and restructure software requirements as needed

• Interpret legislation relating to software testing and update relevant SOPs accordingly

Continuous Improvement

• Contribute to the ongoing improvement of verification processes and documentation

• Drive automation initiatives and improvements in test methods

• Coordinate and, when relevant, delegate testing activities across the Software team

The skills and experience you bring:

 Must‑haves

• Experience with safety‑critical software development, preferably following IEC 62304

• Experience working in an ISO 13485‑controlled environment

• Knowledge of software development and formal software verification

• Experience with automation and optimizing verification processes

• Strong ability to create and maintain technical documentation

• Systematic, analytical, and driven to complete activities with high quality

 Nice‑to‑haves

• Experience with software testing in a medical device‑regulated environment

• Experience contributing to risk management, usability, and design control

• Knowledge of ISO 14971 and/or Software as a Medical Device (SaMD)

How you work:

• You are structured and detail‑oriented, yet able to maintain a high‑level overview

• You take ownership of activities and proactively move tasks forward

• You communicate clearly and collaborate effectively across disciplines

• You embrace continuous improvement and compliance‑driven work

• You are a natural cross-functional facilitator of testing activities

Your qualifications and experience:

• B.Sc. in Software Engineering, Information Technology, Electrical Engineering, or similar field.

• ISTQB certification preferred.

• Minimum 3 years of experience in a similar role.

• Fluency in English written and spoken

The team:

You will join our dedicated Technology team of 10 highly skilled colleagues in engineering, software, and biomedical sciences. Collaboration is key in this tight-knit environment, and the Software Verification Specialist role is central to ensuring product quality and compliance across multiple software components.

Applicants must be eligible to work in Denmark and possess a valid work and residence permit if applicable. At this time, we are unable to support work permit applications or sponsorships.

What we offer:

• A collaborative team with strong professional standards

• A workplace with great energy, social activities, and a culture of togetherness

• A role based in our modern HQ in Allerød with excellent facilities and accessibility

• An opportunity to directly impact verification strategy in a MedTech company committed to improving patient lives.

At UNEEG, your ideas matter, your work makes a difference, and your colleagues have your back.

How to apply and who to contact:

For more details about the job, please contact Senior Director, Technology, Kim Heeggard Hansen, at kimh@uneeg.com

All applications must be in English and are treated confidentially. We will screen and invite candidates for interviews on an ongoing basis so please apply as soon as possible.

About UNEEG Medical

UNEEG Medical pioneers ultra long‑term subcutaneous EEG monitoring to help physicians optimize treatment for epilepsy patients. Our CE‑marked UNEEG EpiSight solution provides objective insights into seizure burden, enabling more personalized care. We collaborate with leading institutions across Europe and the US to help patients regain control of their life. At UNEEG Medical, we are currently 40 dedicated people with diverse backgrounds. Our HQ is in Allerød with subsidiaries in UK, Germany, Austria and the US. Our core values Togetherness, Integrity, and Dedication guide our work as we catalyze brain health therapy with real‑world data.