- Temporary
- Full Time
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Job description
As a (Senior) Project Engineer you will be part of the CMF R&D team, helping our customers and their teams restore form, function and hope to the patients around the world.
With our team, you will be responsible for designing, developing, testing and supporting the physical components (implants) of a system product.
What You Will Do:
In this role you will be part of the product development activities for existing custom CMF implants within an interdisciplinary team.
You will support new product development projects with specification creation throughout finalization, mechanical engineering analysis and prototype realization and will independently work on your own set of tasks in accordance with the project timeline. 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 portion of the documentation work related to hardware topics in coordination with Quality Assurance.
Overall, you act as an important and competent contact person for the tech lead of the project as well as all other relevant stakeholders ( e.g. manufacturing, biomechanical testing lab, quality, and process development departments.)
What you will need:
Required:
Master’s degree in engineering, medical technology or a related field.
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.
Good knowledge of different manufacturing technologies, e.g. CNC milling, 3D printing
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 4 years.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology and Orthopaedics that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
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