RA Manager East Flanders
Location: BelgiumSIRE® 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 Flandre Orientale Belgium.
Leading RA specialists in the registration procedures and submissions to authorities
Communication with local and international regulatory bodies
Preparation and implementation of SOP's
Contribute to the regulatory strategy
Act as the Responsible Person for Information and Publicity
Take care of pharmacovigilance documentation
3-5 years of experience in regulatory affairs for pharmaceuticals
Relevant people management experience
Fluent in Dutch and English, French is highly appreciated
Good knowledge and experience with pharmacovigilance
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Nicolas Gyselinck.
The Company
Our client is a big pharmaceuticals company, based in Ghent, East Flanders. They are a global player on the market of both human and veterinary medicines and are still broadening their focus on different export markets. Because of that, their regulatory activities are growing as well, hence they are currently looking for a new RA manager.Role Description
As the RA manager, you lead the ongoing regulatory projects, ensuring the precise and timely execution. You plan, coordinate and supervise the team of specialists in order to obtain marketing authorisations.Responsibilities
Overseeing the database of registration dossiers and documentsLeading RA specialists in the registration procedures and submissions to authorities
Communication with local and international regulatory bodies
Preparation and implementation of SOP's
Contribute to the regulatory strategy
Act as the Responsible Person for Information and Publicity
Take care of pharmacovigilance documentation
Requirements
At least a bachelor degree in pharmacy or something relevant in life sciences3-5 years of experience in regulatory affairs for pharmaceuticals
Relevant people management experience
Fluent in Dutch and English, French is highly appreciated
Good knowledge and experience with pharmacovigilance
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Nicolas Gyselinck.
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