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!
Our client is a professional Medical Devices organization, based in Limburg Netherlands.
They are an international company with facilities across Europe and America. They are till today still expanding and are therefore looking for a Quality Manager to expand their team and divide the current workload.
As the new Manager in Quality Assurance you will support all quality related issues within the Company. You will be the first contact person concerning quality related production and problems. The new manager will be supervising the quality control within the company and the laboratory. You will implement all new changes regarding the new ISO 13485 and maintain efficient and effective Quality Management Systems that will be implemented and are already implemented.
Besides supervising the quality systems you will work with the current team towards strategy targets and maintain a continuous improvement form a quality point of view. Your responsibilities will lay with especially ISO 134845 and internal audits. As the manager it is your task to supervise and train the quality team to ensure up-to-date knowledge.
• A university degree in science
• A minimum of 5 years experience within the quality assurance (international is preferred)
• Experience with ISO 13485 & 9001 and GMP
• Fluent in English and Dutch and intermediate in German
• Being innovative and able to work independent