Quality Engineer Production Site
Location: BelgiumSIRE 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 Belgium.
This organisation is developing high-technology products across the globe. They established multiple subsidiaries worldwide that all have their own specialty. They are focused on the improvement of our health within society. They are specialists in creating soft- and hardware infrastructures, commonly known as 3D printing. As a continuously growing company they are looking for new specialists.
ROLE DESCRIPTION
In your role as Quality Engineer, you will be operating at the manufacturing site. On a daily basis you will have to establish and maintain relationships with various stakeholders within the organisation. You will overview all activities attached to Quality Assurance of the site. Your major task is to advice the engineers and support the team in relation the QMS. Furthermore, you will be assisting that department in collecting required documentation and regulations. You will directly report to the Quality manager. This role lasts for 3 months and can be extended to 5 months.
RESPONSIBILITIES
Your main task is to be on the site as QA expert that supports and advises various stakeholders which are directly involved in manufacturing. Furthermore, your role includes:
• Gain insight into possible points of improvements for the QMS
• You will be on track with the latest developments and changes of QA within the Medical Devices sector
• Development of strategic plans and implementation tools for the improvement of the Quality Management System
• Overview and collect required documentation and legislation in relation to the product specifications
• Review and assessment of procedures involving risk and validation management at the manufacturing site
REQUIREMENTS
• Bachelor in engineering
• Minimal 4 years of experience within QA in the Medical Devices
• Excellent knowledge of EU and USA regulation for Medical Devices
• A team player, yet strong individual
• Fluency in English and Dutch, Business level French
• Strong communicator and analytical skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Juliette van Kraaij.
