Regulatory Affairs Project
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 Pharmaceutical organization, based in Belgium.
The client is dedicated to improve humans health. They want to improve access to medicines and related health care services to the people who need them.
ROLE DESCRIPTION
You will be responsible for the registration of the clients product and work in a small team of RA specialists. This concerns a project for one to three months.
RESPONSIBILITIES
- Be responsible for the registration of the clients healthcare products
- Timely preparation and approval of country records and related attachments on behalf of the representative
- Be responsible for mapping all relevant submission and approval documents
- Be up-to-date with the regulatory guidelines to maintain Regulatory Affairs department files and be compliant
REQUIREMENTS
- Academic degree in life science
- At least half a year of experience with registration in RA
- Excellent communication and writing skills
- Being fluently in English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.
