REGULATORY AFFAIRS MANAGER
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 Pharmaceutical organization, based in Brussel Belgium.
As a worldwide leader supplying the pharmaceutical and biotechnology industries with biopharmaceuticals.
ROLE DESCRIPTION
As a regulatory affairs manager you will be responsible for the regulatory strategy and global regulatory deliverables for the company.
RESPONSIBILITIES
- Coordination and planning regulatory submissions with management and departments regarding the overall planning to meet customers and project timelines
- Generate a good understanding of the regulatory compliance
- Maintain product registration approvals by ensuring compliance with regulatory requirements and work closely together with Global Regulatory Affairs
- Contribute with regulatory submissions (e.g. DMFs, CEP applications) while collaborating with other functions involved
- Collaborate with Global Regulatory Affairs
- To update and be up-to-date on regulatory legislations, including local regulations and communicate this effectively
REQUIREMENTS
- Minimum bachelor degree in life science related field,
- Minimum of 3 years of experience in the medical affairs in the pharmaceutical industry,
- Experience and knowledge in the pharmaceutical industry, preferably in Regulatory Affairs (CMC)
- Excellent communication and writing skills in French and English
- Experience in leading a team, delegating and decision-making
- Good technical writing skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees van Wezel.
Job Description
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 Pharmaceutical organization, based in Brussel Belgium.
As a worldwide leader supplying the pharmaceutical and biotechnology industries with biopharmaceuticals.
ROLE DESCRIPTION
As a regulatory affairs manager you will be responsible for the regulatory strategy and global regulatory deliverables for the company.
RESPONSIBILITIES
- Coordination and planning regulatory submissions with management and departments regarding the overall planning to meet customers and project timelines
- Generate a good understanding of the regulatory compliance
- Maintain product registration approvals by ensuring compliance with regulatory requirements and work closely together with Global Regulatory Affairs
- Contribute with regulatory submissions (e.g. DMFs, CEP applications) while collaborating with other functions involved
- Collaborate with Global Regulatory Affairs
- To update and be up-to-date on regulatory legislations, including local regulations and communicate this effectively
REQUIREMENTS
- Minimum bachelor degree in life science related field,
- Minimum of 3 years of experience in the medical affairs in the pharmaceutical industry,
- Experience and knowledge in the pharmaceutical industry, preferably in Regulatory Affairs (CMC)
- Excellent communication and writing skills in French and English
- Experience in leading a team, delegating and decision-making
- Good technical writing skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees van Wezel.
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 and Development (R&D)
