Junior Quality Engineer
Location: NetherlandsSIRE 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 Gelderland Netherlands.
They are an international producer of Medical Devices and cleanrooms throughout the world with different facilities and officer in EMEA and America. Due to their growth they are looking for junior QA engineers.
ROLE DESCRIPTION
As the new Junior QA engineer you will support the Benelux region with Quality affairs and am partly responsible for the implementation, maintenance and development of ISO 13485 and FDA regulations. You will be guided by the local QA manager and ensure that the company stays conform the medical regulations.
RESPONSIBILITIES
Apart from being responsible for the Quality Management Systems you will monitor performance and produce statistical reports by gathering the relevant QA data. The Junior QA will support CAPA’s as the CAPA coordinator, participate in internal audits, identify training needs to maintain necessary competencies and ensure QA activities are carried out to safeguard regulation compliancy of the company.
REQUIREMENTS
• At least two years QA experience
• Experience with ISO 13485 & ISO 9001 and FDA
• Fluent in English where Dutch is an added value
• Experience preferably within a Medical Device environment
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Evertsen.
