Build hands-on experience in a medical device company

At UNEEG Medical, we are on a clear mission: improve epilepsy care and 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 combine the agility of a small company with the high standards of the medical device industry.

Your role and team:

We are looking for a Student Assistant who will provide practical support across UNEEG, with a particular focus on regulatory, quality and clinical activities. You will report to our Senior Director, Regulatory & Quality and work closely with colleagues across the organization. This role gives you the opportunity to apply your studies in practice and gain insight into a regulated medical device environment.

Your main responsibilities will be:

• Help update, format and maintain clinical, regulatory and quality documentation

• Participate in complaint investigations and support follow-up documentation

• Help conduct literature searches and compile relevant information for clinical and regulatory use

• Support Read & Understood activities and training documentation in our Quality Management System (QMS)

• Help maintain databases, reference systems and document handling processes

• Provide administrative and ad hoc support to colleagues across UNEEG

You will thrive in this role if you:

• Are studying medicine and technology, biomedical engineering or another relevant technical or health science degree

• Work in a structured and detail-oriented way and take ownership of your tasks

• Are self-driven, curious and comfortable working both independently and with others

• Communicate confidently in English, both written and spoken

• Are skilled in using Microsoft Office and keen to learn new systems

Previous industry experience is not required. Interest in medical devices, quality, regulatory affairs or clinical work is an advantage.

Practical information:

We expect you to work approximately 8-16 hours per week. The role is based at our office in Allerød, and you must be willing and able to commute to the office. We offer flexibility around your studies and exams.

What we offer:

• Relevant hands-on experience and varied tasks across a growing medical device company

• Close collaboration with experienced colleagues who will support your learning

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

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

Who to contact:

For more details about the job, please contact Senior Director, Regulatory & Quality, Camilla Wismar, at +45 4018 4937.

How to apply:

Apply through our Careers site.

All applications must be in English and are treated confidentially. We screen applications and invite candidates for interviews on an ongoing basis.

About UNEEG Medical

UNEEG Medical pioneers ultra long-term subcutaneous EEG monitoring to help physicians optimize treatment for epilepsy patients. Our 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 the 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.