We handle all issues and requests relating to HR, Payroll, Facility, IT and Finance for both companies. Further, we ensure that both UNEEG medical and T&W Engineering are GDPR-compliant and that all colleagues know and abide by GDPR regulations.

In HR and Payroll, we handle all recruitment, day-to-day employment requests from managers and employees, and all requests regarding salary, pension, vacation, and so on. In Finance, we handle all invoices, reporting to our parent company, and other finance-related tasks. Facility is responsible for all tasks relating to our office building as well as event planning.

We work with recruiter companies, furnishing suppliers, caterers and other collaboration partners needed to ensure a trouble-free work experience for all employees in UNEEG medical and T&W Engineering.

The Administration team is a diverse group who handle a large number of work tasks; they come from a variety of educational, professional and personal backgrounds.

Through cross-disciplinary teamwork, we set the direction for the clinical strategies needed to develop new products, and we deliver the clinical documentation that meets regulatory requirements.

We stay in close contact with end-users of our products, as we coordinate user-validation testing and manage pre- and post-market clinical investigations from planning/start-up to close-out within various indications, including epilepsy, diabetes and sleep.

Based on clinical evidence, we substantiate product claims and support improvement and further development of our products.

The Clinical Affairs team comes from a variety of educational backgrounds, mainly within natural and health sciences, such as pharmaceutical science and biology.

We are a group of data scientists with a good understanding of the physiology of the brain as well as signal characteristics of our special subcutaneous EEG data.

Through signal processing and machine learning, we investigate the feasibility of our technology and develop new findings into novel data-visualisation mock-ups and requirement specifications for future products.

Our scientific background allows us to collaborate with key opinion leaders in academia. We strive to publish our results in peer-reviewed journals and to ensure that they are presented at international conferences.

Team members in Epilepsy Science typically hold an MSc in biomedical engineering or similar degree.

Our work requires various resources within mechanics, electronics and embedded software engineering; all these disciplines must work together in the design and development of the most hassle-free and reliable products to benefit our end users.

Since we work in the field of wearable devices, small size and continuous optimisation are core areas of focus.

We apply a variety of approaches and resources in sourcing components and technology, ensuring usability and ergonomic design, maintaining a network of production and sub-suppliers, building integration with APP interfaces as well as creating internal integration of mechanics, electronics and software.

Team members in Hardware Engineering typically hold a degree in mechanical engineering, electrical engineering or computer science.

We plan, execute and build along with our production partners and R&D. We have a passion for technology and finding the optimal way of assembling different parts into a product with the highest yield and quality. Documenting production, establishing traceability and developing qualified processes for all parts are key to a seamless transfer of design to production.

We often investigate changes to current production, based on design improvements or component obsolescence. We leverage our knowledge of production engineering to investigate and evaluate changes.

Team members in NPI & Production Engineering come from different educational backgrounds, with extensive experience in medical device manufacturing.

We ensure that the voice of the customer is brought into product development, in order to optimise the customer experience and boost the relevance of our product offering.

In addition to our focus on product optimisation and innovation, we are also responsible for overall market-communication strategy and implementation. Through online platforms, we create awareness and support our sales organisation with training and marketing.

We work closely together with colleagues in our organisation. We also have a broad range of external collaboration partners such as epilepsy researchers, subcontractors and translators.

Employees in Marketing & Product Management come from diverse educational backgrounds including business/commercial, communications, biomedical sciences and engineering, healthcare and sales.

Our projects and activities come in all sizes, ranging from small engineering-change programs involving several sub-projects, to development of new products for the epilepsy community.

Our various project teams are staffed with bright minds from the rest of our organisation, such as Marketing, Production, Clinical Affairs, QA/RA and R&D. We also apply external expertise from Danish and international partners.

Key areas of focus for us are delivering projects on time and continuously improving efficiency in project execution.

Our team members typically hold a degree in engineering or have other technical/scientific education, combined with practical experience in product development.

We are involved from the beginning of device design, and remain involved throughout the device life cycle.

Being part of our Quality Assurance and Regulatory Affairs team means that you will be working in close collaboration with stakeholders throughout the organisation, providing professional and proactive support. We offer opportunities to work with quality assurance engineering, quality systems, and regulatory affairs.

Working within Quality Assurance and Regulatory Affairs, you may be involved in a broad range of activities including: maintenance of our quality-management system (QMS), support of manufacturing activities, supplier quality management, complaint investigation, participation in development and change projects, biocompatibility testing, sterilization activities, labelling, conducting regulatory strategies to ensure fast-to-market approach, submission of device files to authorities, regulatory reporting and recalls, and regulatory intelligence.

Members of the Quality Assurance and Regulatory Affairs team come from a variety of educational backgrounds, mainly in natural sciences. Typical backgrounds include biomedical engineering, pharmaceutical science and molecular biology.

We are a group of highly skilled and experienced salespeople who help healthcare professionals improve clinical decision-making, through the use of our ground-breaking solution. We believe in establishing personal connections, and working with our customers to find the best solutions to the many clinical challenges they face.

Through cross-disciplinary teamwork with our colleagues working with clinical affairs, clinical training, and science, we strive to bring new knowledge to our customers with the ultimate aim of improving patient outcomes.

We work closely with internal stakeholders such as our colleagues in Marketing, Product Development and QA/RA to ensure that we develop and document software that is tailored to market needs. We also work with external stakeholders in the epilepsy field to ensure that our software solutions work efficiently with other systems.

The team covers a wide range of technologies and skills such as PC applications, cloud applications and iOS/Android applications. To join our team, you will most likely have a background in computer science, computer engineering, software engineering or medical engineering.

Besides ensuring production and timely delivery of products, we also align activities in the supply chain with commercial sales forecasts to ensure future supply of our medical devices. This includes establishing and managing inventory strategies.

Supply Chain is further responsible for managing CMOs (contract-manufacturing organisations), purchasing raw materials, running the warehouse and shipping products.

Supply Chain is part of R&D and Operations. Our team members come from a variety of educational backgrounds, but are united in our experience with medical device manufacturing.

System Engineering is part of our development organisation. In our teamwork, we thrive by learning from each other and working cross-functionally in development projects with our colleagues in Hardware R&D, Software Development, Clinical Affairs, Regulatory Affairs, Marketing & Product Management and Project Management.

Employees in System Engineering typically have a technical background such as a BSc or MSc degree in mechanical engineering, health technology, software or the like.