Would you like to make an active contribution to ensuring that medical products meet the highest quality and safety standards worldwide? Then MedNet GmbH is the right place for you! As a member of our Regulatory Affairs team, you will take on responsibility and help us shape the future of a dynamic and internationally active company.

MedNet is a leading service provider in the medical technology industry 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 drive 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 will maintain the MDR post-market surveillance system, including the preparation of trend analyses and associated reports.
• You provide support with regulatory customer inquiries and participate in audits by notified bodies and authorities. You carry out internal and external audits in accordance with the requirements of ISO 13485.
• You will work closely with internal departments and external partners to ensure compliance with regulatory requirements.

• You have a degree in natural sciences or medical technology or a comparable qualification.
• You have at least 3 years of professional experience in the field of regulatory affairs for medical devices.
• You 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 will have access to a company pension scheme that offers you secure prospects for the future.
• You benefit from the option of leasing a job bike and enjoy exclusive corporate benefits for employees.
• You can develop professionally and personally in an innovative working environment with regular training opportunities.
• You will experience a modern corporate culture that promotes flexibility, personal responsibility and team spirit.

Would you like to make an active contribution to ensuring that medical products meet the highest quality and safety standards worldwide? Then MedNet GmbH is the right place for you! As a member of our Regulatory Affairs team, you will take on responsibility and help us shape the future of a dynamic and internationally active company.

MedNet is a leading service provider in the medical technology industry 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 drive 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 will maintain the MDR post-market surveillance system, including the preparation of trend analyses and associated reports.
• You provide support with regulatory customer inquiries and participate in audits by notified bodies and authorities. You carry out internal and external audits in accordance with the requirements of ISO 13485.
• You will work closely with internal departments and external partners to ensure compliance with regulatory requirements.

• You have a degree in natural sciences or medical technology or a comparable qualification.
• You have at least 3 years of professional experience in the field of regulatory affairs for medical devices.
• You 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 will have access to a company pension scheme that offers you secure prospects for the future.
• You benefit from the option of leasing a job bike and enjoy exclusive corporate benefits for employees.
• You can develop professionally and personally in an innovative working environment with regular training opportunities.
• You will experience a modern corporate culture that promotes flexibility, personal responsibility and team spirit.

Receipt of your application
We will check your documents carefully and compare your qualifications with the requirements of the position. If any documents are missing, we will contact you as soon as possible.

Get to know us
If we are impressed by your application, we will invite you to an initial interview where we can get to know each other.

Second appointment
In the next step, we will invite you to a second appointment. This will include a tour of our company, where you will gain an initial impression of your potential working environment and get to know our team.‍

Feedback and offer
After the second appointment, you will receive personal feedback. If there is a mutual agreement, we will send you a binding offer. We will give you and us a short time to think things over before finalizing the contract.

A personal process
We design the application process individually and with personal exchange. The process described above serves as a guide, but can be adapted in individual cases.

If you have any questions, please contact Mr. Marko Jokic:
Phone: 0251 32266-57
E-mail: bewerbung@medneteurope.com

We look forward to receiving your application!

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