RA 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 Medical Devices and Pharmaceutical organization, based in Flandre Orientale Belgium.
Our client is a leading european company with focus on innovative health products (OTC).
ROLE DESCRIPTION
To support the Regulatory Team, the company is currently looking for a temporary RA Consultant for 6-months. Your main responsibility is to support the release of two medical devices from regulatory perspective.
RESPONSIBILITIES
- Prepare and submit regulatory dossiers
- Ensure that products meet regulatory requirements
- Liaise with health authorities
- Be up-to-date on changing regulatory guidelines
REQUIREMENTS
- Academic degree in Pharmacy or Life Sciences
- Min. 2+ years' experience in medical devices or pharmaceutical industry
- Knowledge of European regulatory guidelines
- Good communication skills in English (both written and spoken)
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.
