RA Consultant | 6 months | Big Pharma
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 Brussels Hoofdstedelijk Gewest Belgium.
- Coordinating extra studies required for the registration files;
- Maintaining Belgium/Luxembourg registrations by means of preparing, reviewing and submitting of renewals;
- Correct and timely communication of changes to data and dossiers;
- Coordinate changes related to packaging materials;
- Be responsible for every regulatory activity related to non-medicinal products.
- industrial pharmacist is an asset;
- 3-5 years experience
- Preferably trilingual (Dutch, French, English)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
The Company
They are a global pharmaceutical leader that leads the market through innovation in medicine.Role Description
Planning & follow-up of all regulatory activities for dedicated products. Compiling, submission and follow-up of registration files. Assure products are in accordance with pharmaceutical law.Responsibilities
- Preparation and submission of marketing authorisation dossiers;- Coordinating extra studies required for the registration files;
- Maintaining Belgium/Luxembourg registrations by means of preparing, reviewing and submitting of renewals;
- Correct and timely communication of changes to data and dossiers;
- Coordinate changes related to packaging materials;
- Be responsible for every regulatory activity related to non-medicinal products.
Requirements
-MSc in pharmaceutical, biotechnologyy or chemical sciences;- industrial pharmacist is an asset;
- 3-5 years experience
- Preferably trilingual (Dutch, French, English)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
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Job Description
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 Brussels Hoofdstedelijk Gewest Belgium.
- Coordinating extra studies required for the registration files;
- Maintaining Belgium/Luxembourg registrations by means of preparing, reviewing and submitting of renewals;
- Correct and timely communication of changes to data and dossiers;
- Coordinate changes related to packaging materials;
- Be responsible for every regulatory activity related to non-medicinal products.
- industrial pharmacist is an asset;
- 3-5 years experience
- Preferably trilingual (Dutch, French, English)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
The Company
They are a global pharmaceutical leader that leads the market through innovation in medicine.Role Description
Planning & follow-up of all regulatory activities for dedicated products. Compiling, submission and follow-up of registration files. Assure products are in accordance with pharmaceutical law.Responsibilities
- Preparation and submission of marketing authorisation dossiers;- Coordinating extra studies required for the registration files;
- Maintaining Belgium/Luxembourg registrations by means of preparing, reviewing and submitting of renewals;
- Correct and timely communication of changes to data and dossiers;
- Coordinate changes related to packaging materials;
- Be responsible for every regulatory activity related to non-medicinal products.
Requirements
-MSc in pharmaceutical, biotechnologyy or chemical sciences;- industrial pharmacist is an asset;
- 3-5 years experience
- Preferably trilingual (Dutch, French, English)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Research & Development (R&D)