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26.07.2016

Sr Development Engineer

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Medical Devices organization, based in Germany.

-Great (design-) scope of tasks in a young company
-Community working climate in a motivated team
-Innovative product portfolio in a worldwide growing market
-Attractive surroundings in the south of Stuttgart by public transport connection
-Assistance in finding accommodation in the Stuttgart area
-Performance-based compensation

ROLE DESCRIPTION

In a flat hierarchy this professional will work within a team in the development department.

RESPONSIBILITIES

-Development of disc replacement implants (cages) and related instruments
-Join and control the development process of implants from blueprint to market launch
-3D design and drawing
-Safely select organization of prototypes and pilot series
-Conducting usability tests
-Development-related cooperation with doctors
-Creation of test and validation plans and the related reports
-Assistance with documentation and execution of the design transfers

REQUIREMENTS

-Degree in medical technology, mechanical engineering, precision engineering or possess a comparable focus in medical technology
-4-5 years of professional experience in the development of orthopedic medical devices
-Familiar with the customary regulations such as ISO 13485, ISO 14971 and QSR 21 CFR 820
-Very good knowledge of 3D CAD, ideally in SolidWorks
-Very good knowledge of MS Office
-High level of technical knowledge
-motivated team player with the ability to motivate others
-Good to very good knowledge of English

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Matthias Kunkel.



 
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