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Registration Specialist

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SIRE 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 Agriculture, Chemicals and Pharmaceutical organization, based in Brabant Flamand Belgium. Our valued client develops thousands of new molecules every year. From a strategic point of view, they are mainly dedicated to research and development registration and positioning of new molecules. On the other hand, they have reinforced their local marketing organizations in recent years and also have established marketing alliances with a number of other multinational and national companies.

Role description

The Regulatory Affairs Team has 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.


Substance responsibility – no direct management of substance at entry level but 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 / Will be able to redefine priorities
People management
• Relationship management
• Initiative/problem solving


• Essential
• 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)
• Previous experience (none to two years) with legislative and regulatory process in plant protection is especially helpful.
• Flexibility, assertiveness and ability to independently and efficiently work in an interdisciplinary and international team
• Fluent in English
Highly Desirable
• Additional language skills would be an asset
• Self-motivated

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SIRE Life Sciences

Ref. number: 35156
Listed by: SIRE Life Sciences
Listed on: 20-07-2017
Country: Belgium
Region: Brabant Flamand
Employment: Permanent
Expertise: 3 - 5 years
Location Type: On location
Language: English
Sector: Pharmaceutical
Specialisation: Regulatory Affairs

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