Regulatory Affairs Specialist (gn) Medizintechnik

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Regulatory Affairs Specialist (gn) Medizintechnik, Nuremberg

Client:

Location:

Nuremberg, Germany

Job Category:

Other

EU work permit required:

Yes

Job Reference:

3e6ff6065aa1

Job Views:

3

Posted:

18.02.2025

Expiry Date:

04.04.2025

Job Description:

Regulatory Affairs Specialist (gn) Medizintechnik

AQUITAS specializes in personnel consulting and placement in the Nuremberg area. All our job offers are thus permanent and full-time positions with our clients. Through close cooperation with the companies, we can ideally support you in the application process and offer you individual support. Currently, we are looking for a Regulatory Affairs Specialist (gn) Medizintechnik for a company in the medical technology sector located in Nuremberg. With several hundred employees, our client specializes in the development and manufacture of medical technology products and devices... and is waiting for you!

What is offered:

• Exciting tasks in a growing company
• An attractive salary with profit sharing
• A company restaurant and a large supply of fruit for a delicious but also healthy lunch break
• Flexible working hours through flexitime and remote work
• Subsidy for public transport
• Flat hierarchies with quick decision-making processes
• Individual training opportunities

These tasks will motivate you:

• As a Regulatory Affairs Specialist (gn), you will be responsible for ensuring compliance with global regulatory requirements for medical technology products
• You will accompany development projects and take over the review and approval of development and accompanying documents
• You will keep an eye on international regulatory requirements and communicate with the relevant authorities to ensure product approvals
• Moreover, you will integrate the regulatory requirements into the product development process
• In addition, you will coordinate with relevant stakeholders for seamless international market entry

Good prerequisites for your success:

• You have a technical degree (ideally in the field of medical technology) or have a comparable qualification
• You have experience in the field of Regulatory Affairs - ideally with experience in an international environment
• Your very good German and English skills round off your profile

What happens next?

Take your chance and apply directly via the online form. Simply upload your documents and you're done. Alternatively, you can also send us an application via email to [emailprotected]. However, since you are not just a resume, we want to get to know you to best support you in the application process. After an initial conversation, we will help you optimize your documents and prepare you for the interview with our clients. I look forward to getting to know you! Best regards, Philip.