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 Netherlands.
They are a worldplayer striving for health and the products to achieve that. They are ambitious, innovative and a large player within the medical devices industry looking for new ambitious professionals.
ROLE DESCRIPTION
As the new Quality engineer you will be responsible for the quality of the devices. By being in contact with other teams, you will guarantee and strive for improvement of this quality every day. You will be working within an ambitious young team where you will be challenged to take on many different projects with many opportunities to grow and develop. The end date to this project is still unknown, expected 3 - 5 months.
RESPONSIBILITIES
In this Quality position you will be responsible for monitoring the production processes, research and prevent possible deviations within this process and hereby reporting said problems. Additional responsibilities will be:
• Reviewing produces batches for deviations
• Carrying out department audits
• Taking care of and/or giving trainings in regards to Quality systems
• Monitoring activities and making sure they comply to current laws and regulations (ISO, GMP)
REQUIREMENTS
• BSc/MSc within a medical device/technologica environment
• 3-5 years of experience within a device production environment
• Fluent in English
• Ambitious and the will to develop yourself
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.
