Development Engineer (m/f) 390276/4

November 2018

Dezember 2019


nicht angegeben




Ihre Aufgaben:
Responsible for the design, development and documentation of existing electromechanical medical devices
Working on independently complex assignments
Acting as a contact person for internal and external technical questions/issues of products on market
Designing, developing and improving electromechanical medical devices according to the product development/ change process
Investigation of issues of products on market (NC, SCAR, CAPA, Complaint)
Performing the required activities and generates the appropriate technical documents to ensure compliance with national and international regulations related to medical devices (EU MDD/MDR, US FDA, Japanese PAL)
Working with manufacturing during the design stages to incorporate manufacturability into the product designs and during the implementation phase
Working with internal shared services (Design Engineering, Quality, Regulatory) and external suppliers to achieve agreed project milestones (e.g. for supplier Change Requests, Design Changes)
Developing with the test team test set-ups (including derivation of benchmarks) and coordinates the activities required to fabricate test parts and complete testing (according to PD process)
Knowledge and compliance with laws and policies that apply to the job and ensure a high level of professionalism, ethics and compliance at all time

Ihre Qualifikationen:
Master/ bachelor’s degree in mechanical or mechatronics engineering
Profound experience in the design and development of medical devices or comparable industries
Business fluent in German and good knowledge of English
Creative/ problem-solving skills
CAD knowledge preferably PTC Creo
Good documentation practice (GDP) knowledge
Analytical skills
Willingness to accept responsibility
Team player

Projektstart: 11/18
Projektdauer: 13 MM

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