Regulatory Affairs Consultant
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 Bruxelles-Capitale Belgium.
Act as technical writer for CMC parts of regulatory variations
Registrations and submissions
Contact with relevant regulatory authorities
Report to the RA director
4 years of experience in regulatory affairs and CMC
Fluent in English, Dutch and French
Willing to travel
Good planning and communication skills
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 consultancy company, based in the capital region of Brussels. They are a global leader in regulatory affairs consulting, providing big multinationals with the right specialist to support their regulatory activities. As the demand for these specialist is growing and the regulatory framework keeps changing, they are looking for a new RA consultant.Role Description
As an RA consultant, it is your job to ensure that the products of the clients are compliant to the regulations, as needed to be able to market the products. You will work on both short and long term projects.Responsibilities
Your responsibilities may vary from one project to another. In most cases you will:Act as technical writer for CMC parts of regulatory variations
Registrations and submissions
Contact with relevant regulatory authorities
Report to the RA director
Requirements
At least a Master degree in a life sciences field4 years of experience in regulatory affairs and CMC
Fluent in English, Dutch and French
Willing to travel
Good planning and communication skills
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.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
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 Bruxelles-Capitale Belgium.
Act as technical writer for CMC parts of regulatory variations
Registrations and submissions
Contact with relevant regulatory authorities
Report to the RA director
4 years of experience in regulatory affairs and CMC
Fluent in English, Dutch and French
Willing to travel
Good planning and communication skills
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 consultancy company, based in the capital region of Brussels. They are a global leader in regulatory affairs consulting, providing big multinationals with the right specialist to support their regulatory activities. As the demand for these specialist is growing and the regulatory framework keeps changing, they are looking for a new RA consultant.Role Description
As an RA consultant, it is your job to ensure that the products of the clients are compliant to the regulations, as needed to be able to market the products. You will work on both short and long term projects.Responsibilities
Your responsibilities may vary from one project to another. In most cases you will:Act as technical writer for CMC parts of regulatory variations
Registrations and submissions
Contact with relevant regulatory authorities
Report to the RA director
Requirements
At least a Master degree in a life sciences field4 years of experience in regulatory affairs and CMC
Fluent in English, Dutch and French
Willing to travel
Good planning and communication skills
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.
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)
