Regulatory Affairs Assistant
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 Brussel Belgium.
Our client is an international leading company within the pharmaceutical market. The company's portfolio mainly encompasses generics and biosimilars.
ROLE DESCRIPTION
Due to a change in regulations for pharmaceutical packaging and labeling, the company is looking for a Regulatory Affairs Assistant who supports the RA team to check the correctness of the updated documents and to perform the administrative work.
Project duration: 1 year
Starting date: 01 September 2017
RESPONSIBILITIES
- Check correctness of updated marketing authorizations documents
- Check correctness of translations from English to Dutch and French
- Support with administration: write cover letters for dossiers, plan RA meetings, keep budgets under control etc.)
REQUIREMENTS
- Degree in Life Sciences, Biology or related field
- Fluency in Dutch and English, good communication in French
- Affinity for regulatory affairs, first experiences are welcome
OTHER
This is a nice opportunity for graduates who want to kick-start their career within the pharmaceutical industry in the field of Regulatory Affairs. During the project you will gain a thorough insight into regulatory procedures and activities and work closely with the QA department.
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.
