What You Will Do: 

In this role you will lead the product & system development activities for existing PEEK custom CMF implants within an interdisciplinary team. 

You will support development projects with specification finalization, mechanical engineering analysis, biomechanical test support and prototype realization and will independently take on the processing of the sub-project management of the hardware area. You will ensure interface communication between software, hardware, and process development. 

You will coordinate and conduct product safety and performance tests in collaboration with the biomechanical testing laboratory and provide support in design validation and product approval.  

You will independently take on a large part of the documentation work regarding hardware topics in coordination with quality. 

Overall, you act as an important and competent contact person for the project manager, manufacturing, marketing, quality, and process development departments. 

What you will need: 

Required: 

Master’s degree in engineering 

You have already gained experience in product and/or system development, project execution & verification & validation.

Excellent interpersonal skills – high degree of independence, communication skills as well as a structured and solution-oriented approach to work.

You enjoy delving into new problems and familiarizing yourself with them.  

Excellent written and spoken German and English skills round off your profile.  

Preferred:  

3-5 years of professional experience in product development, project execution & verification & validation.

Good knowledge of biomechanical testing, materials, and process design. 

Experience in a highly regulated industry, preferably in medical devices 

Diversity is important to us. We welcome applications from people regardless of their ethnic, national or social origin, gender, disability, age or sexual identity.  

This position is initially limited to 24 months.