We are seeking a talented and highly motivated software developer to join our development team. As part of the development team, you will collaborate with team members to create medical device software. The team works in a regulated environment that requires disciplined work habits.
Function &amp; Responsibilities
<ul data-pattern="discCircleSquare" data-depth="1">
<li>Test automation.</li>
<li>Software development.</li>
<li>Contribute to the architecture design of the software.</li>
<li>Contribute to the software development process, including writing test specifications.</li>
</ul>

Education and Qualification requirements
<ul data-pattern="discCircleSquare" data-depth="1">
<li>B.Sc. in Engineering, Computer Science, Data Science or related fields or equivalent professional experience.</li>
<li>Experience with python.</li>
<li>Familiarity with .Net desktop application development.</li>
<li>Experience with Scrum, CI/CD and test automation.</li>
<li>Excellent oral and written communication skills to support quality documentation of engineering actions and assessments within the applicable QMS.</li>
<li>Experience with git (version control).</li>
<li>Experience with CI/CD. </li>
</ul>
<ul data-pattern="discCircleSquare" data-depth="1"></ul>
The job application, CV, and cover letter may be submitted in English or Icelandic.

We are always interested in talented individuals who share our passion for improving people&rsquo;s lives. Nox Medical embraces diversity. As an equal opportunities employer, we believe the foundation of our dynamic and pioneering spirit starts with a fair and inclusive culture. Our company culture focuses on bringing unique ideas and people together to spark innovation and teamwork.

Nox Medical is a med-tech company that builds solutions for healthcare providers to diagnose sleep disorders. We offer devices, software, cloud and AI solutions that are at the forefront of the sleep medicine industry. 

We are a part of Nox Health, which is a global sleep health leader on a mission to improve the health of populations through better sleep. Every year, more than three million people in 50 countries benefit from Nox products and services. Nox provides a range of solutions from comprehensive sleep diagnostic technology for providers to value-based comprehensive sleep management programs for self-insured employers and payers.

Nox Medical


We are seeking a talented and highly motivated software developer to join our development team. As part of the development team, you will collaborate with team members to create medical device software. The team works in a regulated environment that requires disciplined work habits.

Function &amp; Responsibilities


 - Test automation.

 - Software development.

 - Contribute to the architecture design of the software.

 - Contribute to the software development process, including writing test specifications.




Education and Qualification requirements


 - B.Sc. in Engineering, Computer Science, Data Science or related fields or equivalent professional experience.

 - Experience with python.

 - Familiarity with .Net desktop application development.

 - Experience with Scrum, CI/CD and test automation.

 - Excellent oral and written communication skills to support quality documentation of engineering actions and assessments within the applicable QMS.

 - Experience with git (version control).

 - Experience with CI/CD.





The job application, CV, and cover letter may be submitted in English or Icelandic.



We are always interested in talented individuals who share our passion for improving people’s lives. Nox Medical embraces diversity. As an equal opportunities employer, we believe the foundation of our dynamic and pioneering spirit starts with a fair and inclusive culture. Our company culture focuses on bringing unique ideas and people together to spark innovation and teamwork.

Active

Software Development Engineer

We are looking for an ambitious and detail-oriented individual to join our regulatory team, which is responsible for the company&rsquo;s compliance with applicable laws and regulations relating to medical device manufacturers. The Regulatory Affairs Specialist will participate in cross-functional projects relating to the design and development of medical devices, market registrations, and implementation/improvement projects to ensure regulatory compliance of the manufacturer and the medical device throughout its life cycle.
Function &amp; Responsibilities
<ul>
<li>
Prepare regulatory documents for medical device submissions.
</li>
<li>
Compiling technical documentation data packets for distributors to support international product registration.
</li>
<li>
Participates in creating and maintaining technical documentation (TD) to comply with EU MDR and other country/market-specific requirements for TD
</li>
<li>
Participates in developing, implementing and maintaining the necessary internal procedures to ensure the company&rsquo;s ongoing compliance with national and international regulations/requirements
</li>
<li>
Participates in improvement projects related to the Quality Management System
</li>
<li>
Research applicable national and international standards and guidance to provide input to the company&rsquo;s ongoing compliance and medical device state-of-the-art status
</li>
<li>
Participates in design reviews and conducts regulatory assessment/gap analysis
</li>
<li>
Participates in market surveillance of medical devices
</li>
<li>
Provide support during audits conducted by Notified Body (NB)/Conformity Assessment Bodies (CAB) and Regulatory Authorities (RA) and formulate the appropriate response and corrective actions
</li>
</ul>
Education and Qualification requirements
<ul>
<li>
B.Sc degree in Biomedicine, Engineering, or other relevant education or equivalent experience required in regulatory affairs within the medical devices or pharmaceutical industry or equivalent
</li>
<li>
Good planning/organizational and problem-solving skills and techniques
</li>
<li>
Exercise judgment within defined procedures and practices to determine appropriate action
</li>
<li>
Technological skills with the capability to understand the product technology/design as well as tests, standards, guidance, and other methodologies needed to demonstrate and maintain compliance with applicable regulations
</li>
<li>
Experience with medical device regulatory affairs, submissions, compliance programs, and quality systems is preferred
</li>
<li>
Excellent English skills, both verbal and written
</li>
</ul>
The right person for the position
<ul>
<li>
You have an analytical ability as you will be performing assessments and evaluations
</li>
<li>
You have strong communication skills working within a collaborative environment
</li>
<li>
You need to have strong attention to detail as you will be assisting with ensuring and maintaining compliance of the medical devices throughout their lifetime
</li>
<li>
You need to be organized and comfortable managing multiple work tasks
</li>
</ul>
The Job application, CV, and cover letter may be submitted in English or Icelandic.
We are always interested in talented individuals who share our passion for improving people&rsquo;s lives. Nox Medical embraces diversity. As an equal opportunities employer, we believe the foundation of our dynamic and pioneering spirit starts with a fair and inclusive culture. Our company culture focuses on bringing unique ideas and people together to spark innovation and teamwork.


We are looking for an ambitious and detail-oriented individual to join our regulatory team, which is responsible for the company’s compliance with applicable laws and regulations relating to medical device manufacturers. The Regulatory Affairs Specialist will participate in cross-functional projects relating to the design and development of medical devices, market registrations, and implementation/improvement projects to ensure regulatory compliance of the manufacturer and the medical device throughout its life cycle.

Function &amp; Responsibilities


 - 

Prepare regulatory documents for medical device submissions.


 - 

Compiling technical documentation data packets for distributors to support international product registration.


 - 

Participates in creating and maintaining technical documentation (TD) to comply with EU MDR and other country/market-specific requirements for TD


 - 

Participates in developing, implementing and maintaining the necessary internal procedures to ensure the company’s ongoing compliance with national and international regulations/requirements


 - 

Participates in improvement projects related to the Quality Management System


 - 

Research applicable national and international standards and guidance to provide input to the company’s ongoing compliance and medical device state-of-the-art status


 - 

Participates in design reviews and conducts regulatory assessment/gap analysis


 - 

Participates in market surveillance of medical devices


 - 

Provide support during audits conducted by Notified Body (NB)/Conformity Assessment Bodies (CAB) and Regulatory Authorities (RA) and formulate the appropriate response and corrective actions



Education and Qualification requirements


 - 

B.Sc degree in Biomedicine, Engineering, or other relevant education or equivalent experience required in regulatory affairs within the medical devices or pharmaceutical industry or equivalent


 - 

Good planning/organizational and problem-solving skills and techniques


 - 

Exercise judgment within defined procedures and practices to determine appropriate action


 - 

Technological skills with the capability to understand the product technology/design as well as tests, standards, guidance, and other methodologies needed to demonstrate and maintain compliance with applicable regulations


 - 

Experience with medical device regulatory affairs, submissions, compliance programs, and quality systems is preferred


 - 

Excellent English skills, both verbal and written



The right person for the position


 - 

You have an analytical ability as you will be performing assessments and evaluations


 - 

You have strong communication skills working within a collaborative environment


 - 

You need to have strong attention to detail as you will be assisting with ensuring and maintaining compliance of the medical devices throughout their lifetime


 - 

You need to be organized and comfortable managing multiple work tasks



The Job application, CV, and cover letter may be submitted in English or Icelandic.

We are always interested in talented individuals who share our passion for improving people’s lives. Nox Medical embraces diversity. As an equal opportunities employer, we believe the foundation of our dynamic and pioneering spirit starts with a fair and inclusive culture. Our company culture focuses on bringing unique ideas and people together to spark innovation and teamwork.

Regulatory Affairs Specialist

We are looking for a Supply Chain Coordinator to support our global operations. In this role, you will help ensure seamless material flow, accurate documentation, and timely deliveries, which are key elements in maintaining optimal performance across our manufacturing and distribution operations.
Key Responsibilities
<ul>
<li aria-level="1">
Create, track, and update purchase orders to ensure on-time delivery.
</li>
<li aria-level="1">
Monitor inventory levels and flag shortages or excess.
</li>
<li aria-level="1">
Coordinate with suppliers, logistics partners, and internal teams to resolve order or delivery issues.
</li>
<li aria-level="1">
Maintain accurate purchasing records and support reporting on costs and supplier performance.
</li>
<li aria-level="1">
Support QA activities and contribute to process and efficiency improvements.
</li>
</ul>
Qualifications
<ul>
<li aria-level="1">
Bachelor&rsquo;s degree or equivalent experience in supply chain, logistics, or a related field.
</li>
<li aria-level="1">
1&ndash;2 years of experience in supply chain, logistics, or administrative support.
</li>
<li aria-level="1">
Strong organizational and analytical skills, attention to detail, and ability to manage multiple tasks.
</li>
<li aria-level="1">
Good communication skills and proficiency in English (written and spoken).
</li>
<li aria-level="1">
Ability to work confidently with ERP systems (e.g., Business Central, Navision).
</li>
</ul>
&nbsp;
At Nox Medical, you&rsquo;ll join a team of passionate professionals dedicated to improving health through sleep. We foster a culture of innovation, collaboration, and learning&mdash;where your work directly impacts healthcare outcomes worldwide.
Applications are due by January 4th, 2026. Please submit your application, CV and cover letter in English.


We are looking for a Supply Chain Coordinator to support our global operations. In this role, you will help ensure seamless material flow, accurate documentation, and timely deliveries, which are key elements in maintaining optimal performance across our manufacturing and distribution operations.

Key Responsibilities


 - 

Create, track, and update purchase orders to ensure on-time delivery.


 - 

Monitor inventory levels and flag shortages or excess.


 - 

Coordinate with suppliers, logistics partners, and internal teams to resolve order or delivery issues.


 - 

Maintain accurate purchasing records and support reporting on costs and supplier performance.


 - 

Support QA activities and contribute to process and efficiency improvements.



Qualifications


 - 

Bachelor’s degree or equivalent experience in supply chain, logistics, or a related field.


 - 

1–2 years of experience in supply chain, logistics, or administrative support.


 - 

Strong organizational and analytical skills, attention to detail, and ability to manage multiple tasks.


 - 

Good communication skills and proficiency in English (written and spoken).


 - 

Ability to work confidently with ERP systems (e.g., Business Central, Navision).






At Nox Medical, you’ll join a team of passionate professionals dedicated to improving health through sleep. We foster a culture of innovation, collaboration, and learning—where your work directly impacts healthcare outcomes worldwide.

Applications are due by January 4th, 2026. Please submit your application, CV and cover letter in English.