Would you like to actively contribute to ensuring that medical devices meet the highest quality and safety standards worldwide? Then MedNet GmbH is the right place for you! By strengthening our Regulatory Affairs team, you will take on responsibility and shape the future of a dynamic and internationally active company with us.

MedNet is a leading service provider in the medical technology sector with a broad international network of partners and customers. We find smart solutions for a sustainable future and give our employees the space they need for new ideas. In our company with a family culture and strong values, around 60 colleagues are driving progress in medical technology. As a medium-sized company with over 30 years of experience, we offer you the warm and open atmosphere of a modern company in a fast-growing and future-proof industry.

• You create and maintain technical documentation for class I-III medical devices in accordance with MDR (EU 2017/745).
• You maintain the MDR post-market surveillance system, including preparation of trend analyses and related reports.
• You assist with regulatory customer inquiries and participate in audits by notified bodies and authorities. They carry out internal and external audits in accordance with ISO 13485 requirements.
• You work closely with internal departments and external partners to ensure compliance with regulatory requirements.

• You have completed a degree in natural sciences or medical technology or a comparable qualification.
• You have at least 3 years of professional experience in regulatory affairs for medical devices.
• They have in-depth knowledge of MDR and ISO 13485 as well as experience in working with notified bodies and authorities.
• You are fluent in German and English and work in a structured and independent manner.

• You get access to a company pension plan that offers you secure future prospects.
• You benefit from the opportunity to lease a job bike and take advantage of exclusive corporate benefits for employees.
• You can develop professionally and personally in an innovative working environment through regular continuing education opportunities.
• You will experience a modern corporate culture that promotes flexibility, personal responsibility and team spirit.

Would you like to actively contribute to ensuring that medical devices meet the highest quality and safety standards worldwide? Then MedNet GmbH is the right place for you! By strengthening our Regulatory Affairs team, you will take on responsibility and shape the future of a dynamic and internationally active company with us.

MedNet is a leading service provider in the medical technology sector with a broad international network of partners and customers. We find smart solutions for a sustainable future and give our employees the space they need for new ideas. In our company with a family culture and strong values, around 60 colleagues are driving progress in medical technology. As a medium-sized company with over 30 years of experience, we offer you the warm and open atmosphere of a modern company in a fast-growing and future-proof industry.

• You create and maintain technical documentation for class I-III medical devices in accordance with MDR (EU 2017/745).
• You maintain the MDR post-market surveillance system, including preparation of trend analyses and related reports.
• You assist with regulatory customer inquiries and participate in audits by notified bodies and authorities. They carry out internal and external audits in accordance with ISO 13485 requirements.
• You work closely with internal departments and external partners to ensure compliance with regulatory requirements.

• You have completed a degree in natural sciences or medical technology or a comparable qualification.
• You have at least 3 years of professional experience in regulatory affairs for medical devices.
• They have in-depth knowledge of MDR and ISO 13485 as well as experience in working with notified bodies and authorities.
• You are fluent in German and English and work in a structured and independent manner.

• You get access to a company pension plan that offers you secure future prospects.
• You benefit from the opportunity to lease a job bike and take advantage of exclusive corporate benefits for employees.
• You can develop professionally and personally in an innovative working environment through regular continuing education opportunities.
• You will experience a modern corporate culture that promotes flexibility, personal responsibility and team spirit.

If you are ready to take on responsibility in a future-oriented company and actively shape its commercial direction, we look forward to receiving your application!

Submission of Your Application
We will carefully review your documents and compare your qualifications with the position’s requirements. If any documents are missing, we will contact you promptly.

Initial Meeting
If your application impresses us, we will invite you to an initial conversation to get to know each other.

Second Appointment
As the next step, we will invite you for a second meeting. This includes a tour of our company, giving you the opportunity to gain your first impressions of your potential work environment and meet our team.

Feedback and Offer
After the second meeting, you will receive personal feedback. If we find common ground, we will send you a formal job offer. Both sides will have a brief period to consider before finalizing the contract.

A Personalized Process
We tailor the application process with a focus on personal interaction. The steps outlined above serve as a guideline and may be adjusted on a case-by-case basis.

If you have any questions, please feel free to contact Mr. Marko Jokic:
Phone: +49 251 32266-57
Email: bewerbung@medneteurope.com

We look forward to your application!