SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation.
We like technology, in a Life Sciences 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 organisation, based in Limburg Belgium.
This organisation has an extensive portfolio of Medical Devices. Their products vary from endoscopy to interventional oncology.
They are internationally represented and currently experience a growth for their EMEA site.
In your role as Regulatory Affairs specialist, you will gain the responsibility to collect, maintain and adjust technical files and relevant documentation.
You will have a supportive role in creating awareness and exchange of knowledge about international regulations and changes.
In addition, you interact with internal and external stakeholders and you will ensure that they are provided with the required information.
Next to that, you are involved in the development of strategic plans which are related to the Regulatory Affairs and the implementation.
This project is set for a year and can possibly be extended.
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.