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05.09.2016

Quality Technician (m/f)

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.

Our client is an international class III medical device company. It develops and manufactures cardiovascular related electronical products to prevent heart failure. The position will be located in Niedersachsen, Germany.

ROLE DESCRIPTION

The Quality Technician is responsible for conducting testing procedures and ensures that products comply with quality standards. Demonstrating quality in all aspects of the work life. That incluedes verifying compliance to DMR/QSR and conducting product failure analysis as well as post market activities.

RESPONSIBILITIES

·Testing the received products
·Collection and documentation of test data results
·Supporting validation and verfication activities
·Auditing activities for compliance according to different standards (QSR/ISO/cGMP)
·Root cause analysis of customer post market complaints in collaboration with other departments
·Product evaluation and Identification of CAPA

REQUIREMENTS

· 3-5 years of relevant electrical or technical experience necessary. Experience in the medical device industry is preferable
·Good knowledge within ISO/FDA quality standards and GMP
·Professional skills in MS-Office
·Strong language skills in English and German
·Ability to work effectively in a team environment as well as independently

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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