Regulatory Affairs Specialist
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, Chemicals and Pharmaceutical organization, based in Belgium.
The company is a well positioned international client, who develops thousands of new molecules every year. They are dedicated to research and development registration and positioning of new molecules. Having the opportunity to learn and grow is a given, since you’ll be working in an encouraging and inspiring surrounding.
ROLE DESCRIPTION
The team you'll join, has the primary responsibility for approval / renewal active substances at EU level under Regulation 1107/2009 and for the processing of applications to obtain, maintain and renew registrations for plant protection products in the EMEA region. More specific, the port-folio management in Italy and Croatia (EU and Balkan countries will be under your responsibilities.
RESPONSIBILITIES
- Substance responsibility – provide assistance to the (Senior) Registration Specialists
- Country responsibility – registration requirements in order to maintain, extent, and obtain processes
- Expertise responsibility – develop expertise, have good overview, and assist in processes
- Project management – responsible for the maintenance and development of project management tool / enable to work independently and interact well with individuals form of other disciplines to achieve regulatory objectives and to ensure compliance with corporate policies and international regulations, and defined timeframes
REQUIREMENTS
- Minimum of a master degree (preferably in physico-chemistry) but other scientific specialization may be considered as well (such as, but not limited to, toxicology, ecotoxicology, environmental-fate, chemistry)
- Previous experience (2+ years) with legislative and regulatory process is a plus
- Flexibility, assertiveness and ability to independently and efficiently work in an interdisciplinary and international team
- Fluent in English
- Additional language skills would be an asset (especially Italian, Croatian)
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.
