- Location
- Ballerup, Denmark
- Type
- Full-time
- Department
- Legal
- Closing date
- Today
- Source
- Workday
Description
As Regulatory & Lifecycle Compliance Specialist in GN Hearing, you will contribute to our purpose of Bringing People Closer, by helping ensure that our hearing aid products remain compliant throughout their lifecycle. You will support regulatory assessments, product changes, documentation, and process improvements that help bring safe and compliant medical devices to market and keep them there. In this role, you will support lifecycle compliance for hearing aids across new products and in‑market devices.
The position is well suited to someone early in their career who is motivated by structured problem-solving, improving how work gets done, collaborating across different functions, while learning across the regulatory and quality aspects of medical devices
The team you will be part of:
At our global HQ in Ballerup, Denmark, you will join the Regulatory & Lifecycle Compliance team and report to the Regulatory & Lifecycle Compliance Manager.
We are a collaborative team where learning, knowledge sharing, and continuous improvement are part of our everyday work. We encourage new ideas and give you the opportunity to develop both your technical and professional skills, while helping bring safe and compliant medical devices to market.
Your contribution is appreciated, and you will:
Support regulatory compliance activities across the lifecycle of hearing aid products.
Contribute to regulatory assessments and product change activities to help maintain continued compliance.
Collaborate with colleagues across functions to support product development and product lifecycle improvements.
Contribute to process improvements and efficient day-to-day ways of working.
Identify opportunities to automate and streamline repetitive tasks using digital tools and AI where relevant.
Support Agile ways of working
Prepare and maintain clear regulatory documentation.
At GN we encourage flexible working when possible. We trust our people to fulfill their responsibilities, to know when in-person collaboration creates the most value, and to be present when it matters most.
To perform well in the role, we imagine that you:
Hold a degree in Engineering or another relevant technical field
Bring relevant experience from studies, internships, student roles, or an early-career position
Have an interest in medical device regulation and quality, with some familiarity with frameworks such as MDR, FDA, ISO 13485, IEC 62304, or IEC 62366, or similar
Understand how to work within procedures, controlled documentation, change control, and audit-ready processes
Take a structured and risk-based approach to your work
Communicate clearly and can adapt technical or regulatory topics to different audiences
Work well both independently and in collaboration with others
Are curious, analytical, and motivated to learn
Are proficient in English, written and spoken
You may be especially effective in this role if you have also worked with or have an interest in:
Automation or digital tools, such as Python, Power Automate or Power BI
AI tools that support efficiency and process improvement
Agile or Scrum ways of working
We encourage you to apply
If your experience does not match every qualification listed, we still encourage you to apply. We know that relevant skills can come from different types of roles, studies, and experiences. We value transferable skills and motivation to learn. We also welcome applications from recent graduates who bring curiosity, structure, and a strong motivation to grow within medical device regulatory and quality work.
We are committed to an inclusive recruitment process
All applicants will receive equal consideration for employment. To support a fair and consistent process, we encourage you to submit your CV without a photo.
If you need any adjustments or accommodations during the interview process, please let the Hiring Manager know when accepting the invitation to interview.
How to apply?
Use the ‘APPLY’ link no later than August 30th, 2026.
On a time crunch? Feel free to only submit your up-to-date CV, including a few sentences outlining your motivation for applying – quick and easy.
Applications are reviewed on a continuous basis, so we encourage you to apply as soon as possible. Please note that we may close the position before August 30th if we identify the final candidate earlier.
Join us in bringing people closer
GN brings people closer through our advanced intelligent hearing, audio, video, and gaming solutions. Inspired by people and motivated by innovation, we develop technology that enhances the senses of hearing and sight. We help people with hearing loss address real-life challenges, improve communication and collaboration for businesses, and create strong experiences for audio and gaming users.
GN Store Nord A/S has entered into a definitive agreement for the sale of GN’s Hearing business to Amplifon S.p.A. to create a global leader in audiology. For GN Group, this creates an opportunity to expand our position in the large audio and video peripherals markets. Read more about the announcement here.
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