SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical organisation, based in Anvers Belgium.

The Company

The company is part of a global pharmaceutical company, active in injectable pharmaceuticals.

Role Description

This interim project will take up to 5 months to cover for maternity leave. You will be part of a regulatory and quality department that is responsible for all products in the Benelux. To make sure that the department remains able to take on the daily workload, you will be required to work preferably full time and on location at the facility in the Antwerp region.

Responsibilities

You will be responsible for the continuity of writing variations for the directions, labels and dossiers. Translations need to be taken care of as well.

Requirements

- Experienced RA officer in the field of pharmaceuticals or medical devices
- Hands-on experience with translations and variations
- Fluent in Dutch, French and English (German would be a nice addition)
- Structured and focused individual that can self regulate

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge.