Regulatory Affairs Consultant
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 Biotechnology and Pharmaceutical organization, based in Brussel Belgium.
The company is one of the leading biotechnology companies in Europe.
ROLE DESCRIPTION
As a Regulatory Affairs Consultant you will be mainly responsible for the coordination and execution of regulatory submissions in compliance with national and European regulatory requirements.
RESPONSIBILITIES
- Guarantee regulatory submissions
- Contribute to and implement the filing plan
- Review source text for country labeling
- Analyze promotional materials
- Keep track on new & ongoing local legislation and regulatory policy
- Coordinate and review briefing documents
- Organizing translation for local Regulatory submission
REQUIREMENTS
- Bachelor or Master degree in Life Science or a similar scientific discipline
- Min. 3+ years' experience in a related field
- Good communication skills in Dutch or French, fluency in English is an additional must
- Excellent organizations skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Anja Paetel.
