Regulatory Affairs Submission Specialst
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 Limburg Belgium.
is a specialist in Medical Devices class II and III
ROLE DESCRIPTION
The role is designed to support the Regulatory Manager in implementing a new product group to the company. Having knowledge on submissions, Technical Files and Dossier making is essential. Both knowledge of CE and approvals outside Europe are essential.
RESPONSIBILITIES
- Technical Files
- Dossier making
- Regulatory of Russia, Turkey Middle East
REQUIREMENTS
- 3-5 year of experience in Medical Devices
- Knowledge of regulatory submissions
- Knowledge of regulations outside of Europe
- Flexible attitude
- Good knowledge of both Dutch and English
- Able to move for the duration of the project
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Tim Thuijs.
